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Pulse sequences for efficient multi-cycle terahertz generation in periodically poled lithium niobate

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Abstract

The use of laser pulse sequences to drive the cascaded difference frequency generation of high energy, high peak-power and multi-cycle terahertz pulses in cryogenically cooled (100 K) periodically poled Lithium Niobate is proposed and studied. Detailed simulations considering the coupled nonlinear interaction of terahertz and optical waves (or pump depletion), show that unprecedented optical-to-terahertz energy conversion efficiencies > 5%, peak electric fields of hundred(s) of mega volts/meter at terahertz pulse durations of hundred(s) of picoseconds can be achieved. The proposed methods are shown to circumvent laser induced damage limitations at Joule-level pumping by 1µm lasers to enable multi-cycle terahertz sources with pulse energies >> 10 milli-joules. Various pulse sequence formats are proposed and analyzed. Numerical calculations for periodically poled structures accounting for cascaded difference frequency generation, self-phase-modulation, cascaded second harmonic generation and laser induced damage are introduced. The physics governing terahertz generation using pulse sequences in this high conversion efficiency regime, limitations and practical considerations are discussed. It is shown that varying the poling period along the crystal length and further reduction of absorption can lead to even higher energy conversion efficiencies >>10%. In addition to numerical calculations, an analytic formulation valid for arbitrary pulse formats and closed-form expressions for important cases are presented. Parameters optimizing conversion efficiency in the 0.1-1 THz range, the corresponding peak electric fields, crystal lengths and terahertz pulse properties are furnished.

© 2016 Optical Society of America

1. Introduction

Multi-cycle or narrowband terahertz pulses in the frequency range of 0.1 to 1 terahertz (THz) have garnered interest as drivers of compact particle acceleration [1,2], coherent X-ray generation [3] and electron beam diagnostics. An impediment to the widespread deployment of these applications has been the inadequate development of accessible sources of narrowband terahertz radiation (hundred(s) of picoseconds (ps) pulse duration) with simultaneously high pulse energy (> 10 milli-joules (mJ)) and peak powers (> 100 Mega-Volt per meter (MV/m) peak electric fields).

Among existing methods, photoconductive switches can be efficient [4] but relatively challenging to scale to high pulse energies, vacuum electronic devices [5] are limited in their frequency of operation and peak powers while free electron lasers [6] are relatively expensive.

With the rapid scaling of laser pulse energies, laser driven approaches employing second order nonlinear processes such as difference frequency generation (DFG) or optical rectification (OR) are promising. However, scaling this approach to high terahertz pulse energies will require achieving high optical-to-terahertz energy conversion efficiencies (or conversion efficiency for short) as well as the development of high energy optical lasers. Here, we describe approaches to improve conversion efficiencies for multi-cycle terahertz generation, which are still relatively low at the sub-percent level. This problem must be distinguished from broadband or single-cycle source development [7–9] where percent level conversion efficiencies have been demonstrated [10–12]. Correspondingly, we only survey work pertinent to multi-cycle or narrowband sources.

Works using quasi-phase-matched (QPM) Gallium Arsenide (GaAs) [13–17] with conversion efficiencies of 10−4, Gallium Phosphide (GaP) [18] with conversion efficiencies of 10−6 have been reported. However, these materials require pumping by 1.3 µm or longer wavelengths where it is still relatively challenging to develop laser technology with the requisite pump pulse energies. Organic materials have produced multi-cycle radiation with 10−5 conversion efficiencies [19] but are also limited by the requirement of optical pumping at wavelengths of 1.3-2µm, large absorption coefficients at lower terahertz frequencies and laser-induced damage.

Lithium niobate (LN) possesses high second order nonlinearity and is compatible with rapidly developing 1µm [20,21] and established 800 nm laser technology. Furthermore, the large absorption in LN maybe reduced by cryogenic cooling. In combination with feasible Joule-class 1 µm lasers and large cross-section crystals, cryogenically cooled LN may thus offer solutions to the problem of high energy multi-cycle terahertz generation.

In LN, multi-cycle THz generation by interfering chirped and delayed copies of a pulse with tilted-pulse-fronts (TPF) has been demonstrated [22,23]. However, TPFs have limitations induced by angular dispersion [24–26] which also affect other non-collinear approaches [27,28]. Collinear geometries based on periodically poled lithium niobate (PPLN) [29–31] could circumvent angular dispersion based limitations but are characterized by a large walk-off between the optical and terahertz radiation. As a result, even the highest conversion efficiency for multi-cycle generation in PPLN crystals at cryogenic temperatures was only 0.1% [31].

For terahertz generation in the frequency range of 0.1 to 1 THz, the conversion efficiency will be limited to the sub-percent level even if every optical photon (300 THz) is converted to a terahertz photon, due to the large quantum defect. To surpass this limitation, repeated energy down-conversion of optical photons or cascaded DFG [32–35] was proposed conceptually. However, methods to utilize this concept and produce large conversion efficiencies at the percent level or more for multi-cycle sources have not been demonstrated or even proposed.

Here, we study a family of approaches comprised of a sequence of pulses that can achieve very high conversion efficiencies > 5% in cryogenically cooled PPLN crystals. Employing a sequence of uniformly spaced pulses in time circumvents walk-off and coherently boosts the generated terahertz field. In combination with the low loss of cryogenically cooled PPLN crystals, this results in ~cm interaction lengths. Additionally, the low dispersion of LN in the 1µm region permits a large number of phase-matched, repeated energy down conversions of the optical pump frequency. Finally, distributing the pump energy over a long sequence mitigates nonlinear phase accumulation. The maximum fluence that can be coupled into a structure is limited by damage and increases with increasing pulse durations. For Joule-level pumping and long pulse sequences, the required PPLN apertures reduce to 1-2 cm2, which has already been demonstrated [36]. As a result, the set of proposed methods can produce the desired terahertz sources with pulse energies >>10 mJ and peak electric fields of hundreds of MV/m. This work dovetails into another set of approaches employing terahertz driven cascaded parametric amplification which yields similar performance [37].

We discuss different approaches to realize a sequence of pulses in time such as direct generation of a burst of pulses, beating multiple frequency lines and interfering chirped and delayed broadband pulses. Related pulse formats have been previously explored in bulk ZnTe [33,38], with TPFs in bulk LN at room temperature [23] and quasi-phase-matched GaAs [14,16]. However, the work presented here is significantly different for a few reasons. Firstly, a different system, i.e. cryogenically cooled PPLN, is studied. Secondly, the emphasis is on feasible designs that enable dramatic cascaded DFG to achieve conversion efficiencies >>1%, particularly under high energy pump conditions. Furthermore, unprecedented studies of the physics in this high conversion efficiency regime, limiting factors and corresponding correction mechanisms are presented. Finally, in this work, the various pulse sequence formats are treated on a common footing to elucidate the overarching mechanisms unifying their behavior.

Since such high conversion efficiencies can only be obtained by cascaded DFG, calculations incorporating pump depletion are imperative. In Section 2, a numerical model for PPLNs which considers the coupled nonlinear interaction of optical and terahertz fields (or pump depletion) is introduced. The model accounts for dispersion, absorption, cascaded DFG, self-phase-modulation (SPM), cascaded second-harmonic-generation (SHG) and laser induced damage. An analytic formulation considering absorption and dispersion based on undepleted pump approximations is provided for arbitrary pulse formats. At low conversion efficiencies, the analytic calculations show excellent agreement with numerical calculations. However, the results deviate as conversion efficiencies of several percent are obtained. In Section 3, the general physics underpinning terahertz generation with pulse sequences is described. Cascaded DFG causes a red-shift and broadening of the optical spectrum (henceforth referred to collectively as cascading effects) which is seen to result in a modification of the phase-matching condition. This results in a drop in conversion efficiency. Varying the PPLN period along the propagation direction and further reduction of absorption by reducing the crystal temperature to 10 K can thus lead to significantly higher conversion efficiencies. In Section 4, the conversion efficiencies, peak terahertz electric fields and terahertz pulse properties produced by various pulse sequence formats over a large parameter space are analyzed. Closed form expressions are provided for each format. In Section 5, various practical considerations such as self-focusing, terahertz diffraction, pump laser architectures and crystal fabrication are discussed.

2. Theory

2.1 Depleted formulation for QPM structures

Since the proposed set of methods is envisaged to operate in the several percent energy conversion efficiency regime where every optical photon yields multiple terahertz photons by cascaded DFG, it is necessary to simultaneously solve for both optical and terahertz spectral components as in Eqs. (1)-(2).

dATHz(Ω,z)dz=α(Ω)2ATHz(Ω,z)jΩ2χ(2)(z)2k(Ω)c20Aop(ω+Ω,z)Aop*(ω,z)ej[k(ω+Ω)k(ω)k(Ω)]zdω
dAop(ω,z)dz=jω2χ(2)(z)2k(ω)c20Aop(ω+Ω,z)ATHz*(Ω,z)ej[k(ω+Ω)k(ω)k(Ω)]zdΩjω2χ(2)(z)2k(ω)c20Aop(ωΩ,z)ATHz(Ω,z)ej[k(ω)k(ωΩ)k(Ω)]zdΩjε0ω0n(ω0)n2,eff2F{Aop(t,z)|Aop(t,z)|2}
In Eq. (1), the spectral component ETHz(Ω,z) of the terahertz electric field at angular frequency Ω propagating in the positive z direction is described by the complex scalarATHz(Ω,z)ejk(Ω)zwhere ATHz(Ω,z) represents the spectral envelope and k(Ω)represents the wave number at Ω (See Appendix A for Fourier transform conventions). The optical laser field contains a number of spectral componentsEop(ω,z)=Aop(ω,z)ejk(ω)z. Here Aop(ω,z)represents the spectral envelope at angular frequency ω and k(ω) is the corresponding wave number.

In Eq. (1), the first term on the right hand side (RHS) accounts for terahertz absorption. The second term on the RHS of Eq. (1) corresponds to the aggregate of all possible DFG processes between various spectral components of the optical field. The periodic inversion of the second order nonlinearity in PPLN crystals is explicitly accounted for by the χ(2)(z) parameter in Eqs. (1)-(2). Explicitly accounting for the exact variation of χ(2)(z) directly considers all orders of forward propagating QPM waves in the PPLN crystal. The specified pulse formats will only permit phase-matching of harmonics of a single terahertz frequency and hence backward phase-matched waves need not be considered.

Equation (2) represents the corresponding evolution of the envelopeAop(ω,z). The first term on the RHS of Eq. (2) represents the generation of optical radiation due to DFG between higher optical frequencies and terahertz radiation. This term is responsible for cascading effects. The second term corresponds to sum-frequency generation (SFG) between lower optical frequency components and terahertz radiation and causes some blue shift of the optical spectrum. The final term corresponds to the cumulative SPM effect which is a third order process.

While second harmonic generation (SHG) is highly phase mismatched in lithium niobate (Δk~106 m−1), phase-mismatched cascaded SHG (not to be confused with cascaded DFG) can influence the optical pump radiation as an effective third order effect [39]. The explicit consideration of SHG would significantly increase computation time. However, they may be accounted for by a cascaded SHG approximation absorbed into the effective nonlinear refractive index n2,effterm (See Appendix B). The optical-to-terahertz energy conversion efficiency (or conversion efficiency) η is readily calculated by aggregating energy over all terahertz spectral components as follows. Here, Fpumpis the input optical pump fluence.

η(z)=πε0c0n(Ω)|A(Ω,z)|2dΩFpump

The model thus presented considers only one spatial dimension since transverse beam effects are not expected to be significant for the large pump beam sizes pertinent to this work. The length scales of transverse effects estimated in Section 5 justify this assumption.

2.2 Analytic formulation for arbitrary pulse formats

In addition to the above depleted calculations, analytic expressions for arbitrary pulse formats using undepleted pump approximations are derived. While they do not account for cascading effects, they show good qualitative and quantitative agreement with full numerical simulations considering cascading effects. These expressions alleviate the computational challenge of exploring the problem over large parametric spaces, provide overview and consistency checks.

We retain only the first term in the Fourier series expansion of χ(2)(z)=m0(2/mπ)sin(mπ/2)χ0(2)ej2mπΛ1 in the second term on the RHS of Eq. (1). Furthermore, the optical wave numbers k(ω+Ω),k(ω)are expanded via a Taylor series around the central angular frequency ω0 of the pump to the second order to result in Eq. (4). Therefore, contrary to Eqs. (1)-(2), only up to the second order of dispersion is considered.

dATHz(Ω,z)dz=α(Ω)2ATHz(Ω,z)jΩ2χeff(2)ejΔkz2k(Ω)c20Aop(ω+Ω)Aop*(ω)ej(β"Ω(ωω0)+β"Ω22)zdω
In Eq. (4),Δk=Ωc1(n(Ω)ng)2πΛ1 is the phase mismatch between the optical pump and generated THz radiation in a PPLN crystal. Here,ng is the optical group refractive index and n(Ω)is the THz phase refractive index at angular frequency Ω. The parameter Λ corresponds to the period of the PPLN crystal. The periodic inversion of the nonlinearity in the material imparts a momentum2πΛ1, which appears in the expression for phase-mismatch. Setting,Δk=0, provides the required QPM period Λ=(fTHz[n(Ω)ng])1c for the phase-matched terahertz frequencyfTHz (not angular frequency).

In Eq. (4), χeff(2) is the effective second order nonlinearity corresponding to the first term in the Fourier series expansion of χ(2)(z)and β"is the group velocity dispersion due to material dispersion (GVD-MD). Equation (4) is then integrated to yield the following analytic expression for the terahertz spectral envelope (See Appendix A for derivation).

ATHz(Ω,z)=jΩχeff(2)n(Ω)c(α(Ω)2jΔk)(Ftω{Aop(t)Aop*(t+β"Ωz)}ej(Δk+β"Ω22)zFtω{|Aop(t)|2}eα(Ω)z2)
In Eq. (5), Ftω{.}corresponds to the Fourier transform between the time (t), and angular frequency (ω) domains. Upon setting β" = 0, we see that the ATHz(Ω,z) is directly proportional to Ftω(|Aop(t)|2) or the Fourier transform of the optical intensity profile. Note that no assumption about the optical spectrum has been made in Eq. (5), i.e. it is valid for an arbitrary optical pump pulse format.

Equation (5) is verified by evaluating it for the case of a single unchirped Gaussian pulse in a lossless PPLN crystal without dispersion. The second order nonlinear coefficientχeff(2)=2deff. The absolute value of the field component squared for this case is shown in Eq. (6). The expression is in agreement with other formulae in the literature [14,40].

|ATHz(Ω,z)|2=Ω2deff2Fpump2c4π2ε02n(ω0)2n2(Ω)eΩ2τ24sinc2(zΔncΩΩTHz2)z2
In Eq. (6), ΩTHz=2πfTHzis the angular frequency of the phase-matched terahertz wave andΔn=n(Ω)ng. Equation (6) illuminates certain important features. For instance, barring effects of absorption, the terahertz conversion efficiency would increase quadratically with terahertz frequency. If phase-matching is broadband, then the sinc2 function is ~1 and the conversion efficiency [Eq. (3)] increases quadratically with crystal length z. However, if phase-matching is narrowband and there is large walk-off between the optical pump and generated terahertz wave (largeΔn), as is the case for LN, the sinc2 function in Eq. (6) will have a small linewidth centered about the phase-matched terahertz frequency fTHz and may be approximated as a Dirac-Delta functionδ(Δnz[ΩΩTHz]/c).Invoking this approximation leads the conversion efficiency η from Eq. (3) to only increase linearly with crystal length z in the absence of absorption. Thus, the walk-off limitation present in lithium niobate may be deduced from Eq. (6).

3. Terahertz generation with pulse sequences: A general discussion

In this paper, three pulse formats suitable for high energy terahertz generation using cryogenically cooled PPLNs are presented. They comprise of (i) a burst of pulses of equal intensity, (ii) a set of quasi-continuous wave (quasi-CW) lines and (iii) interfering chirped and delayed broadband pulses. All of these formats constitute different forms of pulse sequences in time with common underlying physics. In this section, we provide an overview of the overarching mechanisms of terahertz generation using pulse sequences, their limitations and corresponding correction mechanisms.

3.1 Physical motivation: Alleviating walk-off and laser induced damage

Consider the case of a single optical pump pulse propagating through a PPLN crystal phase-matched for terahertz generation at frequencyfTHz. The electric field of the optical pump pulse is aligned with the extraordinary axis of the crystal for maximum nonlinearity. The optical group refractive index ng = 2.21 at 1030 nm, while the terahertz phase refractive index is n(Ω)~5. In the case of such largeΔn=n(Ω)ng, the optical pump pulse walks off very rapidly from the generated terahertz radiation. As a result, rather than adding on top of the already generated terahertz radiation, the optical pump merely adds another cycle to the back of it. This produces only a linear growth of conversion efficiency with length, in accordance with the discussion following Eq. (6).

Secondly, notwithstanding SPM or self-focusing effects, the permissible peak intensity (and hence fluence) of the optical pump pulse is limited by laser-induced damage (or damage). Therefore, continuously increasing the intensity of the pulse is not a feasible solution to scaling conversion efficiencies. Equivalently, this damage limitation prohibits the use of very large pump energies for feasible crystal apertures.

Now consider a sequence of two optical pump pulses instead of just one incident on a cryogenically cooled PPLN with crystal temperature T = 100 K as simulated in Fig. 1(a). The PPLN period Λ = 237.74 µm has a spatially dependent second order nonlinearityχ(2)(z) as shown in Fig. 1. The crystal parameters correspond to Magnesium Oxide (MgO) doped (5% mol.) congruent lithium niobate (See Table 1. for list, Appendix A for details). Each pump pulse (blue) is Gaussian with a transform limited (TL) full-width at half-maximum (FWHM) duration τ=400 fs optimized for terahertz generation at fTHz=0.5 THz (See Section 4.1). If the pump pulses are separated by a time interval Δt corresponding to the time period of the phase-matched terahertz wave T0=fTHz1 = 2ps (or separated by a distance Δz=cng1fTHz1 inside the crystal), the second pump pulse will coherently add to the terahertz electric field (red) generated by the first ultrafast pulse as shown in Fig. 1(b)-(c). In general, a sequence of N pump pulses will serially boost the terahertz field generated by the first pump pulse in the sequence, thereby alleviating walk-off.

 figure: Fig. 1

Fig. 1 (a) A sequence of 2 optical pump pulses of 400 fs duration each separated by the time period T0 (2 ps) corresponding to the inverse of the THz frequency (0.5 THz).(b)-(c) The second pulse coherently boosts the magnitude of the THz field generated by the first pulse.

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Tables Icon

Table 1. Parameters used for analytic and numerical solutions

The laser induced damage threshold intensity Id reduces as the square root of the pulse duration [41]. Consequently, the damage threshold fluence Fd increases as the square root of the pulse duration. The lower limit of the reported values Fd for a pulse duration of 10 ns in lithium niobate is ~1 GW/cm2 [42]. Therefore, we use the following empirical expressions to determine Id and Fd. Among various factors, the quality of anti-reflection coatings, crystal growth methods, choice and concentration of dopants all influence laser-induced damage. For instance, in preliminary tests on MgO doped (5% mol.) congruent lithium niobate crystals, we recorded damage threshold values, four times larger than those in Eq. (7) [43].

Id=1(τd/10ns)1/2GW/cm2
Fd=10(τd/10ns)1/2J/cm2

A sequence of N pump pulses may be considered to have an effective damage threshold pulse duration τd=Nτ, since the time interval between pulses (~ps) is smaller compared to carrier decay time scales (> ns). Therefore, the permissible peak intensity scales asN1/2 but due to the serial reinforcement by N pump pulses, the conversion efficiency increases as N×N1/2 or asN. Simultaneously, the damage fluence also scales asN, which increases the energy loading capacity of the crystal. Thus, the approach of using a sequence of N pump pulses alleviates walk-off, permits larger pump fluences and results in higher conversion efficiencies.

The scenario illustrated in Fig. 1 addresses a case when every pump pulse in the sequence is of equal intensity. However, the above arguments are generally true even when this is not so. It is worth mentioning that the scaling of the damage threshold depends on the envelope of the pulse, which may result in quantitative alterations that is hypothesized above. The ramifications of pulse envelopes on damage shall be reported elsewhere.

3.2 Terahertz generation mechanisms, limiting factors and correction mechanisms

In Fig. 2, we plot the conversion efficiency (η), according to Eq. (3), as a function of PPLN crystal length for a burst of N optical pump pulses of equal intensity. As in Section 3.1, the simulated pump pulses have Gaussian full-width at half maximum (FWHM) durations τ=400 fs, separated by 2 ps each, optimized for generation of 0.5 THz radiation. The remaining material parameters are presented in Table 1.

 figure: Fig. 2

Fig. 2 (a) Analytic undepleted calculations [Eq. (5)] at 300K for pulse trains with N pulses. Large absorption results in low conversion efficiencies (b) Analytic calculations at 100 K showing enhanced conversion efficiencies due to increase in interaction lengths and reduction in absorption.(c) Depleted calculations [Eqs. (1)-(2)] show good agreement with analytic calculations predicting >5% conversion efficiency at 100 K. Drop in conversion efficiency is due to change in phase-matching produced by (d) spectral shift of optical pump. (e) Terahertz spectrum at 0.5 THz with large suppression of higher order modes.

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In Fig. 2(a), undepleted calculations using Eq. (5) at a crystal temperature T = 300 K are presented (PPLN period Λ = 219 µm). From Fig. 2(a), we see that the optimal interaction lengths are < 0.5 cm due to large absorption (~7.5 cm−1 at 0.5 THz), which limits the conversion efficiency to < 1%. In Fig. 2(b), undepleted calculations at a crystal temperature of 100K (Λ = 238 µm) are presented. The interaction lengths increase to ~2 cm due to a reduction in absorption (~1.36 cm−1). The simultaneous increase in interaction length and reduction of absorption drastically enhances conversion efficiencies to 8%.

The values with larger N initially increase at a slower rate since the intensity of a single pulse in the sequence is lower due to damage limitations [Eq. (7a)]. However, due to mitigation of walk-off, they grow monotonically over a longer length, eventually resulting in higher conversion efficiencies. The optimal number of pulses in the sequence will be proportional to the optimal interaction length. Consequently, there is not as much benefit in increasing the number of pump pulses in the sequence from N = 16 to 32 at T = 300K as it is for T = 100 K.

Conversion efficiencies > 0.1%, are only possible when cascading is present, i.e. the optical pump undergoes repeated energy down conversions. Therefore, we evaluate the same cases via numerical solutions to Eqs. (1)-(2) in Fig. 2(c). These depleted pump calculations incorporating cascading effects agree quantitatively and qualitatively with that in Fig. 2(b) during the initial increase of conversion efficiency. However, after reaching a smaller maximum value of ~5% at shorter interaction lengths ~1.5 cm, a fall in conversion efficiency, contrary to the saturation observed in analytic undepleted calculations [Figs. 2(a)-(b)] is seen.

The fall in conversion efficiency is attributed to a change in the phase-matching condition caused by the spectral broadening and red-shift of the optical spectrum due to cascading. In Fig. 2(d), the optical spectrum as a function of crystal length is plotted for the N = 32 case, which shows a steady red-shift due to repeated energy down conversion of the optical photons to terahertz photons. The corresponding terahertz spectrum [Fig. 2(e)] is quasi-monochromatic at 0.5 THz, with a large suppression of higher harmonics.

In Fig. 3(a), we perform simulations to identify the reasons for the drop in conversion efficiency observed in Fig. 2(c). Equations (1)-(2) are solved with various effects switched on or off to identify their relative influence. As in Fig. 2, a burst of 32 pulses of equal intensity, 400 fs each, separated by 2 ps are incident on a PPLN crystal phase-matched for 0.5 THz. When a medium with no dispersion (denoted by β” = 0), no terahertz absorption (α = 0) and no SPM (n2,eff = 0) is assumed, the conversion efficiency even increases to ~30% (blue, solid curve). The inclusion of SPM does little to change this result. This suggests that further reduction of absorption by cooling to 10 K and reduction of phase-slippage by gradually varying the PPLN period along the crystal length can lead to significantly higher conversion efficiencies.

 figure: Fig. 3

Fig. 3 (a). Conversion efficiency as a function of crystal length with various effects selectively switched on or off. The drop in conversion efficiency observed is due to alteration of phase-matching conditions caused by spectral broadening and red-shift of the optical spectrum. Therefore, further abatement of losses and gradual variation of PPLN periods can yield conversion efficiencies >> 5%. (b) Optical spectrum for the case of a dispersion and absorption free medium [blue curve, Fig. 3(a)] shows dramatic red-shift > 100 THz. In comparison, the regular case with both dispersion and absorption at T = 100 K shows significantly lesser red-shift.

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However, when dispersion was switched on but absorption was zero [red, solid curve Fig. 3(a)], the conversion efficiency was dispersion limited. In this case, the change in the phase-matching condition caused by cascading leads to a saturation of conversion efficiency. If absorption was switched on but dispersion was switched off [blue, dashed curve, Fig. 3(a)], phase-slippage is minimal but the conversion efficiency is limited by absorption. Consequently it saturates when the interaction length is on the order of the absorption length, similar to Fig. 2(b). When both dispersion and absorption are switched on [red, dashed curve, Fig. 3(a)], the conversion efficiency drops rapidly after reaching a maximum value. This is because, after phase-matching is compromised and no net energy is transferred to the terahertz field, inclusion of absorption can only lead to an effective dissipation of THz energy. Further inclusion of SPM does not alter the results significantly [green, dashed curve, Fig. 3(a)]. In Fig. 3(b), the optical spectrum corresponding to the case without absorption or dispersion [blue, solid curve in Fig. 3(a)] is depicted. A dramatic spectral red shift and broadening is evident. This red-shift is significantly larger than the regular case [red curve in Fig. 3(b)] which corresponds to a case with dispersion and absorption at 100 K [green-dashed curve in Fig. 3(a)].The simulations in Fig. 3, thus show that the drop in conversion efficiency observed in Fig. 2(c) is caused by the change in phase-matching condition produced by the shift in the optical spectrum due to cascading. However, further mitigation of losses and reduction of phase-slippage can lead to significantly higher conversion efficiencies.

3.3 Temporal properties of terahertz pulses

Here, we examine the properties of terahertz pulses generated by a sequence of optical pump pulses. First, the case of a burst of pump pulses with equal intensity is considered. The understanding is readily extended to other pulse sequence formats.

In Fig. 4(a), a schematic of a burst of optical pump pulses, separated by an interval T0=fTHz1 is depicted. The full-width at half-maximum duration of each pulse is τ. The entire burst has a total duration τp, which is the main quantity influencing the properties of the generated terahertz pulse. In Fig. 4(b), the relative time scales of the optical pump pulse and the generated terahertz pulse are depicted in the top panel. The bottom panel depicts the absorption experienced by the terahertz pulse over its duration. From Fig. 4(b), we see that the first pump pulse in the sequence entering the crystal at time t = 0, emerges after a time Lng1c and with it appears the first terahertz generated near the crystal exit. The terahertz generated by the back of the pump pulse with effective pulse durationτp, at the beginning of the crystal, will emerge after a time LnTHzc1+τp has elapsed. Therefore, the total temporal extent of the terahertz pulse isL(nTHzng)c1+τp. The shape of the terahertz pulse will be determined by overlap with the pump pulse sequence and absorption considerations as follows:

 figure: Fig. 4

Fig. 4 (a). Schematic of a burst of pump pulses of equal intensity. The total duration of the burst is τp. (b) (Top panel) Relative time scales of optical pump and generated THz pulses. The first terahertz to emerge is generated by the front of the optical pulse near the exit of the crystal. The terahertz to emerge last is generated by the back of the optical pulse near the beginning of the crystal. (Bottom) Absorption is least for the terahertz generated near the exit and most for the terahertz generated at the beginning of the crystal. (c) Simulated terahertz field profiles for a burst of 32, 400 fs (FWHM) Gaussian pulses. (d) Intensity of optical pump pulses

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(i) The terahertz radiation emerging first, generated close to the exit of the crystal, is not serially boosted by the subsequent pump pulses in the sequence and will consequently have the smallest amplitude. Thereafter, the overlap of the generated terahertz with other pump pulses in the sequence linearly increases, up until the moment the final pump pulse emerges from the crystal, i.e. at t = LnTHzc1+τp. After this time, the overlap saturates and begins to decline only after t = LnTHzc1. This corresponds to the time when the terahertz radiation generated by the first optical pump pulse in the sequence emerges from the crystal. Naturally, any terahertz generated after this will overlap less with the pump pulse sequence.

(ii) The front of the terahertz pulse, generated close to the crystal exit experiences the least propagation distance and therefore least absorption. The terahertz generated by the front of the pump pulse sequence at the beginning of the crystal propagates through the entire crystal, experiences maximum absorption and emerges after a time LnTHzc1has elapsed. Any terahertz radiation emerging after this time, experiences the same effective loss, since it too has propagated through the entire crystal.

Based on (i)-(ii), we understand the depicted terahertz pulse schematic in Fig. 4(b). It shows an initial increase in amplitude due to overlap and subsequent drop due to absorption. In Figs. 4(c)-(d), we plot the temporal waveforms of the terahertz electric field obtained from simulations. The waveforms are plotted at the location of maximum conversion efficiency.

In Fig. 4(c), the terahertz electric field for a burst of N = 32, τ = 400 fs pulses separated by 2 ps each are incident on a PPLN crystal phase-matched for 0.5 THz is shown. The conversion efficiency is maximized at L = 1.35 cm [See Fig. 2(c)]. The optical pump pulse sequence is depicted in Fig. 4(d). The inset in Fig. 4(d) shows the sequence of pulses separated by 2 ps each, corresponding to generation of 0.5 THz radiation. In line with the previous reasoning, the amplitude of the terahertz electric field increases up until the duration of the pump pulse has elapsed. Thereafter, a decline initially due to increasing absorption is observed. A third steeper drop, corresponding to a decline in overlap occurs at about tLng1c = 123 ps. This corresponds to the time t = LnTHzc1 when the terahertz generated by the front of the pump pulse sequence at the beginning of the crystal has emerged.

In general, sequences of pump pulses, the terahertz electric field is proportional to|Aop(t)|2sin(2πfTHzt), or the convolution of the pump intensity envelope with a sinusoidal function with a frequency of the phase-matched terahertz wave. However, most of the critical time instants described in the overlap process above are similar for various pulse sequence formats.

3.4 Optimizing the number of pulses in a sequence

A recurring theme in the various pulse formats described will be the optimal number of pump pulses in the sequence or the optimal value of the effective pulse duration τp[See Fig. 4(a)]. An intuitive estimate of this is obtained by examining the time scales of the optical pump pulse sequence and generated terahertz pulses as viewed at the end of a crystal of length L in Fig. 4(b). For most efficacious terahertz generation, temporal overlap between optical and terahertz pulses must be maximized. This translates to the conditionτp>L(nTHzng)c1.

However due to absorption delineated in Fig. 4(b), a trade-off exists. Since the absorption saturates after t = LnTHzc1, the fraction of time over which absorption saturation is present must be minimized. Therefore, one would desireτp<L(nTHzng)c1. Considering both constraints, an estimate for the optimal effective pulse length may beτp~L(nTHzng)c1.

The maximum crystal length L = Lmax itself is set by the strongest limitation to terahertz generation. This approximate condition on the value of τp agrees well with various simulations from ensuing sections. Quantitative corrections to this picture appear upon considering details of the pump pulse envelope.

3.5 Simulation methods and parameters

All ensuing calculations assume MgO doped (5% mol.) congruent lithium niobate as the nonlinear material. The crystal temperature is fixed at 100K. Material and other parameters used in the calculations are tabulated below.

The large cascading of the optical spectrum and long terahertz pulses necessitate simulations with large time-bandwidth products. The accuracy of simulations was verified by examining the numerical conservation of total energy (Appendix C). A bandwidth of 300 THz, a frequency resolution of 0.5 GHz and spatial resolution of 1.25 µm is necessary. For PPLN lengths of ≤ 5 cm, this translates to computational domain sizes with dimensions of 600,000 × 40,000 or 24 billion.

The direct optimization of the numerical solution to Eqs. (1)-(2) is thus impractical. Fast analytic calculations based on Eq. (5) are therefore used to obtain optimal pump parameters for maximizing conversion efficiency. Full numerical solutions are then performed to obtain accurate values of (i) conversion efficiency, (ii) peak electric field, (iii) terahertz pulse durations and (iv) optimal crystal lengths corresponding to these optimal pump parameters.

4 Results

4.1 Burst pulse format

We further analyze terahertz generation due to a burst of N pump pulses with equal intensity. The electric field envelope of such a train is given byAop(t)=n=1NE0e2ln2(tnT0)2τ2. Here, τ is the FWHM pulse duration of each pulse. The pulses are separated from each other by a timeT0=fTHz1. The FWHM durationτ=(2ln2)12τe2, where τe2is the e−2 pulse duration. Using Eq. (5), we obtain the following closed form expression for the spectral componentATHz(Ω,z) in the undepleted limit.

ATHz(Ω,z)=jΩχeff(2)(Fpump/N)ej(N1)ΩT02πc2ε0n(ω0)n(Ω)(α(Ω)2jΔk)sin(NΩT02)sin(ΩT02)(eΩ2τ216ln2(1+4(2ln2)2β"2z2τ4)ejΔkzeΩ2τ216ln2eα(Ω)z2)

Inspecting Eq. (8), the optimal value of the pre-factor sin(NΩT02)[sin(ΩT02)]1=NforT0=mfTHz1, or for integral multiples of the time period of the phase-matched terahertz wave as was illustrated in Section 3.1. Assuming this condition, it is evident from Eq. (8) that the conversion efficiency scales as N since the total pump fluence Fpump scales as Ndue to damage limitations. From the first exponential term within brackets, we see how the GVD-MD term β" results in the spreading of the pump pulse in time. The second term within brackets corresponds to terahertz absorption which results in the saturation of conversion efficiency over crystal length [See Fig. 2(a)-(b)]. Forβ"0, the conversion efficiency gradually vanishes due to reduction in peak intensity by spreading of the pulse in time, albeit rather slowly for small β" (e.g. in Table 1.). For example, a τ = 400 fs pulse only suffers a pulse duration increase of less than 5 fs over 2 cm of propagation in lithium niobate. Furthermore, the pulse-spreading effect is less prevalent when the optical spectrum of the pulse is continuously increasing, as is the case with the numerical simulations based on Eqs. (1)-(2).

Equation (8) is sufficient to predict behavior at low conversion efficiencies [sub-percent level, see Fig. 5(c)] when the undepleted pump approximation holds. For instance, it produces good quantitative agreement with the experiments reported in [31]. These experiments involved impinging PPLNs phase-matched for terahertz generation at 552 GHz at 100 K with a single pump pulse from a Titanium Sapphire (Ti:Sa) laser system centered at 800 nm with FWHM durations in the range of 160fs to 190 fs and peak fluences ranging between 16 and 23 mJ/cm2. Corresponding to these parameters, Eq. (8) predicts conversion efficiencies of 0.08-0.13% at 100K which is in agreement with the experimentally reported value of 0.12%. Note, in order to correspond to the experimental situation, Eq. (8) has to be corrected for Fresnel reflections (~54% terahertz transmission for lithium niobate) and averaging effects due to Gaussian transverse intensity variations (a factor of 0.5).

 figure: Fig. 5

Fig. 5 (a) Conversion efficiency (η) as a function of transform limited FWHM pulse duration τ at T = 100K. Optimal τ values are inversely proportional to the generated frequency fTHz (b) η as a function of number of pulses N in the sequence shows initial Nscaling and eventual saturation when the effective pulse length cτp = cN/ fTHz exceeds the walk-off length. (c) Optimal η for various terahertz frequencies and corresponding calculations considering cascading (square markers). η>5% are predicted. (d) Peak free-space (blue) and focused (green) electric fields obtained analytically (solid) and numerically (square markers) predict field strengths approaching GV/m. (e) Number of cycles for various terahertz frequencies.(f) Optimal interaction lengths L obtained analytically (solid) and numerically (square markers). Cascading effects modify phase-matching conditions and reduce interaction lengths in numerical calculations.

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In Fig. 5(a), we plot the conversion efficiency for various τ and number of pump pulses N in the sequence using Eq. (8) and simulation parameters from Table 1. The solid lines in Fig. 5(a) represent the case of N = 2. For a small pump pulse duration τ (i.e. large bandwidth), the dominant limitation is the low pump fluence due to damage limitations. On the other hand, for large τ, there is insufficient bandwidth for efficient terahertz generation. Consequently, an optimal τ is observed which decreases for larger terahertz frequencies. The dashed lines represent the case for N = 4 pulses. The expectation of Nscaling is evident upon comparing the two cases. In Fig. 5(b), we plot the conversion efficiency as a function of N using Eq. (8) at optimal values of τ for variousfTHz. After the initial N scaling, at larger values of N, a saturation of conversion efficiency is observed. This is understood by recognizing that the parameterNT0 assumes the role of the effective pump pulse duration τp described in Section 3.3-3.4. Since it was deduced that the optimal τp~L(nTHzng)c1, the values of N at which saturation of conversion efficiency occurs are expected to be roughlyL(nTHzng)c1/T0. In the undepleted limit, the conversion efficiency begins to saturate at interaction lengths of ~2 cm at 0.5 THz [See Fig. 2(b)]. This translates to a saturation of conversion efficiency for N~100 pulses which is well supported by the calculations in Fig. 5(b).

Figure 5(c) depicts the maximum conversion efficiency obtained by optimizing undepleted calculations based on Eq. (8) over τ, N and crystal length L for various fTHz (blue, solid). For optimal parameters, numerical solutions (square markers) to Eqs. (1)-(2) (i.e. depleted calculations accounting for cascading effects and SPM) are also performed. In general, an increase in conversion efficiency with frequency is observed in the presented frequency range. The scaling is however not quadratic as simplistic expectations from Eqs. (6),(8) suggest due to trade-offs incurred by terahertz absorption. The conversion efficiency may be expected to saturate at even higher terahertz frequencies due to increasing absorption. For lower conversion efficiencies or smaller terahertz frequencies, almost exact quantitative agreement between analytic and numerical calculations is observed. However, at larger terahertz frequencies, greater deviation is observed due to a greater impact of the modification of phase-matching conditions by cascading effects. As described in Section 3, this results in a reduction of the optimal interaction lengths and conversion efficiencies. The properties of the emergent terahertz pulse are also altered. Despite these limitations, conversion efficiencies in excess of 5% at 0.5 THz are still predicted by numerical calculations, which is significantly higher in relation to existing approaches.

In Fig. 5(d), the peak free-space (blue) and focused (green) terahertz electric fields obtained from analytic (solid) and numerical simulations (square markers) are presented. The focused terahertz fields are estimated by scaling the free space values by a factor equal towinfTHz/c, where win is the input beam radius of a pump laser pulse with a total energy of 1J and a flat-top (or top-hat) beam profile. Thus,win=1/πFd, whereFdis the damage threshold fluence. The scaling reflects the reduction in terahertz beam radius from win to ~cfTHz1 (or the terahertz wavelength as may be obtained in linear accelerator structures [1]) upon focusing.

Focused terahertz fields approaching the GV/m range are thus obtained using numerical calculations. Consistent with the case of conversion efficiencies in Fig. 5(c), the numerical calculations for corresponding peak terahertz electric fields are smaller compared to analytically obtained values at larger terahertz frequencies. In Fig. 5(e), the number of terahertz field cycles corresponding to the e−2 pulse durations (full-width) is presented using analytic and numerical calculations. Naturally, lower terahertz frequencies contain smaller number of cycles, due to their longer time period. At 0.5 THz, ~100 cycles or 200 ps terahertz pulses are predicted. While the total temporal extent of terahertz pulses is altered due to the modification of interaction lengths in the case of numerical solutions, due to overlap effects, the e−2 terahertz pulse duration remains roughly similar to analytic calculations. In Fig. 5(f), the optimal interaction lengths obtained from numerical and analytic calculations are plotted. Quantitative agreement at 0.1 THz is obtained, which is consistent with trends from Figs. 5(c)-(e). For larger terahertz frequencies, the modification of phase-matching conditions by cascading leads to shorter interaction lengths for the case of numerical calculations. The optimal crystal lengths obtained above are accessible with current PPLN technology.

4.2 Difference frequency generation with multiple lines

Beating two or more quasi-CW lines, each corresponding to a pulse with transform limited duration of hundreds of picoseconds and central frequency separated by the terahertz frequencyfTHz also generates a sequence of pulses separated by a time intervalT0=fTHz1. The total spectrum of M quasi-CW lines, where each line has a linewidth corresponding to the FWHM pulse duration τ is given byAop(ω)=m=0M1π/4ln2E0τe(ωω02πmfTHz)2τ28ln2. In time, Aop(t) takes the form of a sequence of ‘sub-pulses’, each separated by T0 with peak intensities following a Gaussian envelope (See Appendix B.3). As the number of lines M increase, the duration of the individual ‘sub-pulses’ decrease and the peak intensity increases. However, the sub-pulses are still contained within an overall Gaussian envelope of FWHM duration τ. This impacts the damage threshold intensity and fluence. For a set of M lines, it can be shown that the relevant damage threshold duration τd=τ/M (Appendix B.3). Upon inserting Aop(ω)into Eq. (5), we obtain Eq. (9) in the undepleted limit.

ATHz(Ω,z)=jΩχeff(2)(FpumpM1)e(Ω2πfTHz)2τ216ln2πc2ε0n(ω0)n(Ω)(α(Ω)2jΔk)[sin(π(M1)β"ΩfTHzz)sin(πβ"ΩfTHzz)e2ln2Ω2β"2z22τ2ej(Δk+π(M1)β"ΩfTHz)zeαz2]

The fluence per line isM1Fpump, where Fpump is the total fluence bound by damage [Eq. (7b)] corresponding toτd=τ/M, i.e. Fd=10(τM1/10ns)1/2. The exponential term outside the brackets in Eq. (9) shows the terahertz field centered aboutfTHz. The first exponential term inside the bracket of Eq. (9) represents the spreading of the pump pulses in time by GVD-MD. Note that the pre-factor sin(π(M1)β"ΩfTHzz)sin(πβ"ΩfTHzz)1 is exactly equal to M −1 forβ"=0. This represents the situation where DFG processes between every pair of adjacent lines add up coherently. However, this may be modified for large values of M, fTHzorβ". The second term in Eq. (9) corresponds to terahertz absorption. In the optimal case, the conversion efficiency which is proportional to |ATHz(Ω,z)|2Fpump1 scales asM5/2(M1)2, forFpump=Fd.This yields the optimal condition of M≤5.

Analytic calculations using Eq. (9) in Fig. 6(a) depict the conversion efficiency as a function of τ for variousfTHz at T = 100K. In this case, τ takes on the role of the effective pump pulse duration τp introduced in Section 3.2. Thus, optimal values of τ are approximately equal to L(nTHzng)c1. For example, at 0.5 THz, an optimal τ~200 ps is obtained which unsurprisingly resembles the optimal values of NT0 for the burst pulse format (N~100) in Section 4.1. In Fig. 6(b), the conversion efficiency for various fTHz as a function of the number of lines M is plotted using Eq. (9). As deduced in the preceding paragraph, the optimal number of lines is M ≤ 5 for all frequencies.

 figure: Fig. 6

Fig. 6 (a).Conversion efficiency η as a function of transform limited FWHM duration of each line τ, showing optimal pulse lengths comparable to the walk-off length.(b) η vs number of lines M, showing saturation for large M. (c) Optimal η obtained analytically (solid) and numerically (squares). Numerical simulations predict η >8% at 0.5 THz. Deviations from analysis are due to modification of phase-matching conditions by cascading effects. (d) Peak free-space (blue) and focused (green) electric fields obtained analytically (solid) and numerically (squares) depicting field values > GV/m.(e) Reduced number of terahertz field cycles obtained numerically (squares) is consistent with lower conversion efficiencies and (f) reduced interaction lengths.

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In Fig. 6(c), the optimal conversion efficiency for variousfTHzare calculated analytically Eq. (9) (solid lines) and numerically using Eqs. (1)-(2) (square markers). Conversion efficiencies of > 5% at 0.5 THz are predicted by the numerical calculations including cascading and SPM. As with the previous case, the deviation of numerical from analytic results for larger terahertz frequencies or conversion efficiencies is owed to the greater impact of the modification of phase-matching conditions by cascading effects. In Fig. 6(d), the free-space (blue) and focused terahertz electric fields (green) are shown analytically (solid) and numerically (square markers). Numerical calculations reveal peak focused electric fields of a several hundred MV/m. The lower conversion efficiencies obtained numerically in relation to analytic results yields proportionally smaller peak electric fields. The corresponding number of terahertz cycles obtained analytically and numerically are shown in Fig. 6(e). Due to overlap effects as in the case of Fig. 5(e), the number of cycles remains roughly similar for analytic and numerical calculations. However, in contrast to Section 4.1, due to the Gaussian envelope of the sequence of sub-pulses, the generated terahertz pulse also has a roughly Gaussian shape. As with the burst pulse format, the optimal interaction lengths obtained numerically are smaller compared to those obtained analytically for larger terahertz frequencies due to a modification of phase-matching conditions by cascading effects as evident in Fig. 6(f).

4.3 Chirp and delay

Interfering copies of chirped broadband pulses delayed with respect to each other offers an alternate method of generating a sequence of pulses. Since the bandwidth of the pulse is spread over time, the approach is similar to DFG between two long narrowband pulses. In particular, the method is attractive for use with off-the-shelf high energy broadband 800 nm Ti:Sa lasers. Here, we calculate the efficiency of the approach for cryogenically cooled PPLNs. We consider the optical laser field due to a chirp and delay setup asAop(t)=21/2(E0e2ln2t2τ2ejbt2+E0e2ln2(t+Δt)2τ2ejb(t+Δt)2). Here, τ is the FWHM chirped pulse duration and is related to the FWHM transform limited pulse duration by the chirp rateb=2ln2(ττTL)1. Inserting Aop(t)into Eq. (5), we obtain the expression for the terahertz spectral envelope ATHz(Ω,z) as follows.

ATHz(Ω,z)=jΩ(Fpump/2)ejΩΔt2πε02c2n(ω0)n(Ω)(α(Ω)2jΔk)[PTHz(Ω,Δt')ejΔkzPTHz(Ω,Δt)eαz2]
PTHz(Ω,Δt)=ε0χeff(2)e(Ω2bΔt)2τ216ln2e2ln2Δt22τ2
Δt'=Δtβ"Ωz

The total pump fluence Fpump is bound by damage according to Eq. (7b). The damage threshold duration is equal to that of two narrowband pulses or the case of M = 2 from Section 4.2 and is given by τd = τ/2. Equation (10b) indicates that the generated terahertz is centered about the terahertz frequencyfTHz=bΔt/π. Thus, the center frequency can be tuned with an appropriate chirp rate b and delay Δt. However, a large delay causes PTHz(Ω,Δt)to drop due to insufficient overlap as evident in the exponential dependence on –Δt2 in Eq. (10b).

In Fig. 7(a), the conversion efficiency η is plotted for various transform limited FWHM pulse durations τTL and terahertz frequenciesfTHzat T = 100K. At low values of τTL, the GVD-MD term in Eq. (10c) leads to lower values of η. At large values of τTL, there is insufficient bandwidth for efficient terahertz generation. The dotted lines correspond to a τ = 50 ps, whereas the solid lines correspond to τ = 100 ps. The similarity of their optima indicate that τTL and τ maybe treated as independent variables. In Fig. 7(b), we plot the conversion efficiency as a function of the chirped pulse duration τ at the optimum bandwidth values obtained from Fig. 7(a). In this case, τ assumes the form of the effective pulse duration τp. Similar to the burst pulse format and the case of M quasi-CW lines, the optimal values of τ also closely resemble the valueL(nTHzng)c1 as deduced in section 3.2.

 figure: Fig. 7

Fig. 7 (a). Conversion efficiency η as a function of transform limited FWHM pulse duration τTL. Low values are limited by dispersion [Eq. (10c)] and large values have insufficient bandwidth.(b) Optimal pulse length is close the walk-off length and is smaller for larger frequencies due to more absorption. (c) Optimal η obtained analytically (solid) and numerically (squares). η ~2% is predicted using numerical simulations. (d) Focused electric field gradients in the range of GV/m are predicted which is in close agreement with numerical results. (e) Numerical results predict shorter terahertz pulse lengths due to (f) shorter interaction lengths.

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For example, in Fig. 7(b), the optimal chirped pulse duration τ = 200 ps at 0.5 THz which is similar to the values obtained for both the M quasi-CW line case [Fig. 6(a)], as well as the burst pulse case [Fig. 5(b)]. The conversion efficiencies obtained with the chirp and delay approach will be similar but lesser than the case with M = 2 quasi-CW lines [See Fig. 6(b),7(b)] due to the eln2Δt2τ2factor produced by the relative delay between optical pulses in Eq. (10b). In Fig. 7(c), the optimal conversion efficiency as a function of terahertz frequency is plotted along with numerical calculations at the corresponding points. Consistent with earlier depicted trends in Section 4.1 and 4.2, the conversion efficiency obtained via numerical calculations are smaller at larger terahertz frequencies due to a more adverse impact of the modification of phase-matching conditions by cascading effects. Despite these limitations, conversion efficiencies of ~2% are predicted at 0.5 THz. The peak terahertz fields are plotted in Fig. 7(d) and corresponding numbers of cycles are plotted in Fig. 7(e). As with prior cases (Section 4.2, 4.3), the peak electric fields obtained numerically are smaller than the analytic values at larger terahertz frequencies due to modification of phase-matching conditions by cascading effects. Focused field strengths of few 100 MV/m are observed. The obtained number of terahertz field cycles is similar for numerical and analytic calculations, consistent with the trends from Section 4.2-4.3. The reduction of interaction lengths due to cascading effects is evident in Fig. 7(f) for larger frequencies as in other pulse sequence formats.

5. Practical considerations

Self-focusing

Since our studies were limited to one dimensional spatial calculations, we calculate self-focusing distances [48] as follows:

zsf=πwin2λ012πn2,effIn(λ0)
Here λ0 is the central wavelength of the optical pump, n2,eff is the effective nonlinear refractive index (Table 1.), win is the input pump beam radius and I is the peak pump intensity. The peak intensity is calculated considering laser induced damage limitations from Eq. (7a) and is proportional toτd1/2. win is calculated assuming a total energy of 1 Joule in the pump pulse sequence and a flat-top beam profile. Due to damage fluence limitations from Eq. (7b),win2=1/(Fdπ)is proportional toτd1/2. From Eq. (11), the dependencies on τd of I andwincompensate each other, resulting in zsf being independent of τd and equal to ~75 cm. This means that self-focusing would not pose an issue as long as operation is below the damage threshold. The caveat however is that τdhas to be large enough to permit values of win that can be accommodated within feasible crystals. However, this would not be true for beams with local spatial modulations. This issue could be circumvented with a suitable imaging system to clean up the beam prior to the PPLN.

Diffraction of terahertz beams

For an optical pump beam radiuswin, the terahertz beam radius would be win/2as a virtue of being generated by a second order nonlinear process. The Rayleigh length (as defined for a Gaussian beam) for a terahertz wave propagating inside the crystal is given by Eq. (12).

zR=12πwin2nTHzfTHzc
In Fig. 8, we plot the damage limited beam radiiwin, Rayleigh and self-focusing lengths at 0.5 THz as a function of the effective pulse durationτd.

 figure: Fig. 8

Fig. 8 Self-focusing, terahertz Rayleigh lengths and requisite crystal apertures as a function of τd. Crystal apertures are within the grasp of current technology, self-focusing and diffraction lengths are longer than the optimal interaction lengths.

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Crystal fabrication

For effective damage threshold durations τd=100-500 ps, the maximum crystal apertures (2win×2win) required would be < 1.2 cm2, which can be realized with demonstrated technology [36].

Multi-photon absorption

For pump wavelengths in the range of ~1 µm, 4-photon absorption of the fundamental and 2-photon absorption of the second harmonic are possible. The former is expected to be weak even for intensities as large as 100 GWcm−2 [25,49], while the latter is not expected to be significant since the SHG is not phase-matched. However, for 800 nm, 3-photon absorption of the fundamental and 2-photon absorption of second harmonic + fundamental is possible [50]. These multi-photon processes are stronger than those for the case of ~1µm wavelengths. Therefore, for 800 nm, lower damage thresholds and conversion efficiencies are anticipated.

Practical implementation of the pulse formats

To generate highly efficient terahertz fields, three pulse formats – a burst of pulses, multiple quasi-CW lines and chirped and delayed broadband pulses have been presented. From a laser engineering point of view, the chirp and delay pulse format can be readily implemented with existing Titanium Sapphire lasers. It involves stretching of a pulse (which is typically done anyway during chirped pulse amplification), splitting and delaying it. However, high pulse energies from Titanium sapphire lasers are typically limited to low repetition rates. For higher average powers, Ytterbium based lasers [20,21] are strong candidates. However, the limited bandwidth of these lasers makes chirp and delay approaches less attractive. Therefore, a burst of pulses with a pulse separation of just a few picoseconds can be achieved by splitting and delaying one laser pulse. The multiple quasi-CW line approach relies on spatially superimposing multiple highly stable narrow band lasers. Such multi quasi-CW line sources may also be self-generated starting with a single quasi-CW pump and weak quasi-CW optical seed pulse. The terahertz radiation, initially generated by the DFG between the pump and seed pulse then rapidly causes the optical spectrum to cascade, thus generating a series of quasi-CW lines [37].

6. Conclusion

Highly efficient terahertz generation approaches employing cascaded difference frequency generation (DFG) of pulse sequences in periodically poled lithium niobate (PPLN) were proposed and analyzed over a large parameter space. Optimal energy conversion efficiencies > 5%, peak electric fields of several hundred MV/m for terahertz pulses with hundreds of picoseconds durations are predicted using calculations employing pump depletion. At Joule level pumping, this translates to terahertz pulse energies >> 10 mJ. Analytic formulations for calculating the conversion efficiencies for arbitrary pulse formats were presented which included the effects of dispersion and absorption. These showed good qualitative and quantitative agreement with detailed numerical simulations including cascaded DFG, self-phase modulation, cascaded second harmonic generation and laser induced damage, particularly at low conversion efficiencies and terahertz frequencies. The physics of terahertz generation using pulse sequences in PPLN’s was discussed. At sufficiently high conversion efficiencies, significant cascading of the optical spectrum results in a change in the phase-matching condition, thereby limiting conversion efficiency. Changing the PPLN period along the propagation direction and further mitigation of losses could lead to even higher conversion efficiencies >>10%. Various practical considerations such as terahertz diffraction, self-focusing, multi-photon absorption, pump laser development and PPLN fabrication were discussed.

Appendix A Analytic formulation

The Fourier transform of a functionf(t)is given byf(ω)=f(t)ejωtdt. The corresponding inverse Fourier transform is defined asf(t)=(2π)1f(ω)ejωtdω. The definitions follow energy conservation (Parseval’s theorem) according to|f(t)|2dt=2π|f(ω)|2dω.

Derivation of Eq. (5)

SettingATHz(Ω,z)=ϕ(Ω,z)eα(Ω)z2reduces Eq. (4) to the following forω0>>0, where Δω=ωω0 is the displacement from the central angular frequency of the pump.

ϕ(Ω,z)=ε0χeff(2)0zAop(Δω+Ω)Aop*(Δω)ej(Δk+β"ΔωΩ+β"Ω22)zeαz2dzdΔω
Forβ"ΔωΩ<<α, the above reduces to the following.

ATHz(Ω,z)=ε0χeff(2)0Aop(Δω+Ω)Aop*(Δω)[ej(Δk+β"ΔωΩ+β"Ω22)zeα(Ω)z2α(Ω)2jΔk]dΔω. The integral, 0Aop(Δω+Ω)Aop*(Δω)dΔωmay be written asF(|Aop(t)|2), upon expressing Aop(Δω+Ω)=(2π)1Aop(t)ej(Δω+Ω)tdtand reversing the order of integrals [51]. Proceeding along similar lines for other integrals, Eq. (5) is obtained.

Appendix B Simulation details

B.1 Material properties

Since the terahertz frequency is much smaller than the optical frequency, the relevant second order nonlinear effect is the electro-optic effect. The electro-optic tensor element which maximizes terahertz generation in lithium niobate isr33. This corresponds to extraordinarily polarized terahertz and optical fields. For lithium niobate, r33~ 32 pm/V. The effective nonlinear coefficient for bulk lithium niobate at a pump wavelength λ0 is then d0=r33n(λ0)4/4 [44]. At 1030 nm, n(λ0)=2.15, which yields a d0=168 pm/V. The corresponding bulk susceptibility is thenχ0(2)=2d0. In PPLN structures, there is periodic inversion of the nonlinearity along the crystal direction z, which is described byχ(2)(z)=χ0(2)sgn{cos(2πΛ1z)}, where sgn is the signum function.

The terahertz absorption coefficients at 300 K and 100 K are obtained from [45,46] in Fig. 9(a). At 0.5 THz, the absorption coefficient at 300 K is 7.2 cm−1. At 100 K, the value reduces to about 1.4 cm−1, representing a fivefold decrease. Even further decrease in absorption may be obtained by cooling the crystal to 10K, which yields an absorption coefficient of 0.25cm−1 at 0.5 THz [46]. In Fig. 9(b), the PPLN poling period Λ for terahertz generation at various frequencies fTHz is obtained in the phase-matched condition asΛ=cfTHz1(nTHz(Ω)ng(λ0))1. The terahertz phase index at 0.5 THz is nTHz(Ω) ~ 4.96 at 300 K and 4.73 at 100 K [45]. The group refractive index is ng(λ0) =2.21 and is relatively insensitive to temperature change.

 figure: Fig. 9

Fig. 9 (a) Terahertz absorption coefficients at various crystal temperatures.(b) PPLN periods for various phase-matched terahertz frequencies at different crystal temperatures (c) Values of n2,eff obtained using Eq. (13) at different crystal temperatures.

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Second harmonic generation is highly phase-mismatched in bulk lithium niobate. Corresponding to the fundamental at 1030 nm with refractive index 2.15, the second harmonic at 515 nm has a refractive index nSHG = 2.24. The corresponding phase-mismatch Δk =1.02×106m−1, which corresponds to a coherence length of πΔk1~ 3 µm that is significantly smaller than the PPLN periods under consideration. However, phase-mismatched SHG can manifest itself as a third order nonlinearity which can considerably alter the self-phase-modulation effect. These cascaded SHG effects have an effective third order susceptibility given by the following [39].

χ(3)casc=m16πdm23nSHGλ01Δkm
χ(3)=χ(3)casc+χ(3)bulk

Here, dm=2dSHG(mπ)1sin(mπ/2) is the mth term in the Fourier series expansion of dSHG(z)=dSHGsgn{cos(2πΛ1z)}and Δkm=4πcλ01[nSHGn(λ0)]2πmΛ1is the mth order phase-mismatch. The value of dSHG = 25 pm/V for lithium niobate. The total third order susceptibility is given by Eq. (13b). χ(3)bulk includes instantaneous Kerr and Stimulated Raman Scattering (SRS) contributions and has a value of 6365 pm2/V2 [39]. The cascaded SHG contribution has a sign opposite of χ(3)bulkand amounts to χcasc(3) = −4428.8 pm2/V2 in bulk LN (obtained by settingdm=dSHGδm,0, where δis the Dirac-Delta function). In bulk LN, this results in a total χ(3) = 1936.2 pm2/V2. The corresponding nonlinear refractive index coefficient n2,eff=3χ(3)/4n(λ0)2ε0c is then equal to 1.17 × 10−19 m2/Watt, similar to reported values [52]. In Fig. 9(c), we plot the calculated n2,efffor PPLNs at various THz frequencies and crystal temperatures. Equation (13) is used for the calculations, with values ranging over negative and positive orders upto the 10th order withm0.

B.2 Numerical diagnostics

In Fig. 10, we present the total energy (or fluence in the 1-D case) for the simulation in Section 3. Absorption is turned off to test the conservation of energy. As can be seen, energy is conserved very well over the simulated crystal lengths.

 figure: Fig. 10

Fig. 10 Verification of the numerical conservation of energy in the simulations.

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B.3 Pulse sequence formats

Consider a pair of quasi-CW lines, separated by the desired terahertz frequencyfTHz. Each quasi-CW line has a linewidth corresponding to a transform limited full-width at half-maximum (FWHM) duration τ. In the time domain, such a spectrum corresponds to an intensity |Aop(t)|2that is proportional to e4ln2t2τ2|ej2πfTHzt+1|2ore4ln2t2τ2cos2(πfTHzt). The corresponding intensity profile is a Gaussian envelope with FWHM duration τ, containing a sinusoidal modulation which appears as a sequence of ‘sub-pulses’ separated by the time period of the terahertz wave T0=fTHz1 in time. The FWHM duration of each sub-pulse is obtained by settingcos2(πfTHzt)=1/2. This yields a sub-pulse FWHM duration of T0/2. The total number of pulses in an envelope with FWHM duration τ is N=τ/T0. The effective damage threshold durationτd which is N times the individual sub-pulse duration is thenτd=NT0/2=(T01τ)T0/2=τ/2. If there are M lines instead of just 2, the envelope retains a FWHM duration τ but the additional bandwidth results in proportionally shorter ‘sub-pulse’ durations [Fig. 11(a)]. Therefore, τd=τ/M for arbitrary M.

 figure: Fig. 11

Fig. 11 (a). Temporal intensity profile corresponding to a spectrum with M quasi-CW lines, each corresponding to a FWHM duration τ = 200 ps and separated by the terahertz frequency fTHz = 0.5 THz. A sequence of ‘sub-pulses’ in time, separated by the time period of the terahertz wave T0 = 2 ps are obtained. The duration of the sub-pulses reduces with increasing M. (b) Temporal intensity profile corresponding to the overlap of two broadband pulses with transform limited duration τTL = 30fs, chirped to τ = 200ps. A sequence of sub-pulses separated by T0 = 2 ps is obtained. The case is similar to that of M = 2 quasi-CW lines.

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Similarly, when two broadband chirped pulses are overlapped with a suitable delay, |Aop(t)|2becomes proportional to e4ln2t2τ2cos2(btΔt+ϕ) which is also a Gaussian envelope with sinusoidal modulations [See Fig. 11(b)]. Since2bΔt=2πfTHz, this also appears as a sequence of ‘sub-pulses’ separated by T0 with a sub-pulse durationT0/2. Therefore, τd=τ/2for chirp and delay approaches.

Funding

European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013) / ERC Grant Agreement n. 609920, the Center for Free-Electron Laser Science at DESY and the excellence cluster “The Hamburg Centre for Ultrafast Imaging- Structure, Dynamics and Control of Matter at the Atomic Scale” of the Deutsche Forschungsgemeinschaft.

Acknowledgments

The authors thank Prof. Erich.P.Ippen for helpful comments and Dr. Sergio Carbajo for initial laser induced damage threshold characterization.

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Figures (11)

Fig. 1
Fig. 1 (a) A sequence of 2 optical pump pulses of 400 fs duration each separated by the time period T0 (2 ps) corresponding to the inverse of the THz frequency (0.5 THz).(b)-(c) The second pulse coherently boosts the magnitude of the THz field generated by the first pulse.
Fig. 2
Fig. 2 (a) Analytic undepleted calculations [Eq. (5)] at 300K for pulse trains with N pulses. Large absorption results in low conversion efficiencies (b) Analytic calculations at 100 K showing enhanced conversion efficiencies due to increase in interaction lengths and reduction in absorption.(c) Depleted calculations [Eqs. (1)-(2)] show good agreement with analytic calculations predicting >5% conversion efficiency at 100 K. Drop in conversion efficiency is due to change in phase-matching produced by (d) spectral shift of optical pump. (e) Terahertz spectrum at 0.5 THz with large suppression of higher order modes.
Fig. 3
Fig. 3 (a). Conversion efficiency as a function of crystal length with various effects selectively switched on or off. The drop in conversion efficiency observed is due to alteration of phase-matching conditions caused by spectral broadening and red-shift of the optical spectrum. Therefore, further abatement of losses and gradual variation of PPLN periods can yield conversion efficiencies >> 5%. (b) Optical spectrum for the case of a dispersion and absorption free medium [blue curve, Fig. 3(a)] shows dramatic red-shift > 100 THz. In comparison, the regular case with both dispersion and absorption at T = 100 K shows significantly lesser red-shift.
Fig. 4
Fig. 4 (a). Schematic of a burst of pump pulses of equal intensity. The total duration of the burst is τp. (b) (Top panel) Relative time scales of optical pump and generated THz pulses. The first terahertz to emerge is generated by the front of the optical pulse near the exit of the crystal. The terahertz to emerge last is generated by the back of the optical pulse near the beginning of the crystal. (Bottom) Absorption is least for the terahertz generated near the exit and most for the terahertz generated at the beginning of the crystal. (c) Simulated terahertz field profiles for a burst of 32, 400 fs (FWHM) Gaussian pulses. (d) Intensity of optical pump pulses
Fig. 5
Fig. 5 (a) Conversion efficiency (η) as a function of transform limited FWHM pulse duration τ at T = 100K. Optimal τ values are inversely proportional to the generated frequency fTHz (b) η as a function of number of pulses N in the sequence shows initial N scaling and eventual saturation when the effective pulse length cτp = cN/ fTHz exceeds the walk-off length. (c) Optimal η for various terahertz frequencies and corresponding calculations considering cascading (square markers). η>5% are predicted. (d) Peak free-space (blue) and focused (green) electric fields obtained analytically (solid) and numerically (square markers) predict field strengths approaching GV/m. (e) Number of cycles for various terahertz frequencies.(f) Optimal interaction lengths L obtained analytically (solid) and numerically (square markers). Cascading effects modify phase-matching conditions and reduce interaction lengths in numerical calculations.
Fig. 6
Fig. 6 (a).Conversion efficiency η as a function of transform limited FWHM duration of each line τ, showing optimal pulse lengths comparable to the walk-off length.(b) η vs number of lines M, showing saturation for large M. (c) Optimal η obtained analytically (solid) and numerically (squares). Numerical simulations predict η >8% at 0.5 THz. Deviations from analysis are due to modification of phase-matching conditions by cascading effects. (d) Peak free-space (blue) and focused (green) electric fields obtained analytically (solid) and numerically (squares) depicting field values > GV/m.(e) Reduced number of terahertz field cycles obtained numerically (squares) is consistent with lower conversion efficiencies and (f) reduced interaction lengths.
Fig. 7
Fig. 7 (a). Conversion efficiency η as a function of transform limited FWHM pulse duration τTL. Low values are limited by dispersion [Eq. (10c)] and large values have insufficient bandwidth.(b) Optimal pulse length is close the walk-off length and is smaller for larger frequencies due to more absorption. (c) Optimal η obtained analytically (solid) and numerically (squares). η ~2% is predicted using numerical simulations. (d) Focused electric field gradients in the range of GV/m are predicted which is in close agreement with numerical results. (e) Numerical results predict shorter terahertz pulse lengths due to (f) shorter interaction lengths.
Fig. 8
Fig. 8 Self-focusing, terahertz Rayleigh lengths and requisite crystal apertures as a function of τd. Crystal apertures are within the grasp of current technology, self-focusing and diffraction lengths are longer than the optimal interaction lengths.
Fig. 9
Fig. 9 (a) Terahertz absorption coefficients at various crystal temperatures.(b) PPLN periods for various phase-matched terahertz frequencies at different crystal temperatures (c) Values of n2,eff obtained using Eq. (13) at different crystal temperatures.
Fig. 10
Fig. 10 Verification of the numerical conservation of energy in the simulations.
Fig. 11
Fig. 11 (a). Temporal intensity profile corresponding to a spectrum with M quasi-CW lines, each corresponding to a FWHM duration τ = 200 ps and separated by the terahertz frequency fTHz = 0.5 THz. A sequence of ‘sub-pulses’ in time, separated by the time period of the terahertz wave T0 = 2 ps are obtained. The duration of the sub-pulses reduces with increasing M. (b) Temporal intensity profile corresponding to the overlap of two broadband pulses with transform limited duration τTL = 30fs, chirped to τ = 200ps. A sequence of sub-pulses separated by T0 = 2 ps is obtained. The case is similar to that of M = 2 quasi-CW lines.

Tables (1)

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Table 1 Parameters used for analytic and numerical solutions

Equations (18)

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d A THz (Ω,z) dz = α(Ω) 2 A THz (Ω,z) j Ω 2 χ (2) (z) 2k(Ω) c 2 0 A op (ω+Ω,z) A op * (ω,z) e j[ k(ω+Ω)k(ω)k(Ω) ]z dω
d A op (ω,z) dz = j ω 2 χ (2) (z) 2k(ω) c 2 0 A op (ω+Ω,z) A THz * (Ω,z) e j[ k(ω+Ω)k(ω)k(Ω) ]z dΩ j ω 2 χ (2) (z) 2k(ω) c 2 0 A op (ωΩ,z) A THz (Ω,z) e j[ k(ω)k(ωΩ)k(Ω) ]z dΩ j ε 0 ω 0 n( ω 0 ) n 2,eff 2 F{ A op (t,z) | A op (t,z) | 2 }
η(z)= π ε 0 c 0 n(Ω) | A(Ω,z) | 2 dΩ F pump
d A THz (Ω,z) dz = α(Ω) 2 A THz (Ω,z) j Ω 2 χ eff (2) e jΔkz 2k(Ω) c 2 0 A op (ω+Ω) A op *(ω) e j( β"Ω( ω ω 0 )+ β" Ω 2 2 )z dω
A THz (Ω,z)= jΩ χ eff (2) n(Ω)c( α(Ω)2jΔk ) ( F tω { A op (t) A op * (t+β"Ωz) } e j( Δk+ β" Ω 2 2 )z F tω { | A op (t) | 2 } e α(Ω)z 2 )
| A THz (Ω,z) | 2 = Ω 2 d eff 2 F pump 2 c 4 π 2 ε 0 2 n ( ω 0 ) 2 n 2 (Ω) e Ω 2 τ 2 4 sin c 2 ( zΔn c Ω Ω THz 2 ) z 2
I d =1 ( τ d /10ns ) 1/2 GW/ cm 2
F d =10 ( τ d /10ns ) 1/2 J/ cm 2
A THz (Ω,z)= jΩ χ eff (2) ( F pump /N ) e j(N1)Ω T 0 2 π c 2 ε 0 n( ω 0 )n(Ω)( α(Ω)2jΔk ) sin( NΩ T 0 2 ) sin( Ω T 0 2 ) ( e Ω 2 τ 2 16ln2 ( 1+ 4 (2ln2) 2 β " 2 z 2 τ 4 ) e jΔkz e Ω 2 τ 2 16ln2 e α(Ω)z 2 )
A THz (Ω,z)= jΩ χ eff (2) ( F pump M 1 ) e ( Ω2π f THz ) 2 τ 2 16ln2 π c 2 ε 0 n( ω 0 )n(Ω)( α(Ω)2jΔk ) [ sin( π( M1 )β"Ω f THz z ) sin( πβ"Ω f THz z ) e 2ln2 Ω 2 β " 2 z 2 2 τ 2 e j( Δk+π( M1 )β"Ω f THz )z e αz 2 ]
A THz (Ω,z)= jΩ( F pump /2 ) e jΩΔt 2 π ε 0 2 c 2 n( ω 0 )n(Ω)( α(Ω)2jΔk ) [ P THz (Ω,Δt') e jΔkz P THz (Ω,Δt) e αz 2 ]
P THz (Ω,Δt)= ε 0 χ eff (2) e ( Ω2bΔt ) 2 τ 2 16ln2 e 2ln2Δ t 2 2 τ 2
Δt'=Δtβ"Ωz
z sf = π w in 2 λ 0 1 2π n 2,eff In( λ 0 )
z R = 1 2 π w in 2 n THz f THz c
ϕ(Ω,z)= ε 0 χ eff (2) 0 z A op (Δω+Ω) A op *(Δω) e j( Δk+ β " ΔωΩ+ β" Ω 2 2 )z e αz 2 dzdΔω
χ (3) casc = m 16π d m 2 3 n SHG λ 0 1 Δ k m
χ (3) = χ (3) casc + χ (3) bulk
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