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Extension of high-order harmonic generation cutoff from laser-ablated tin plasma plumes

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Abstract

The high-order harmonic spectra from laser-ablated tin plasma plumes are investigated experimentally and theoretically at different laser wavelengths. It is found that the harmonic cutoff is extended to ∼84 eV and the harmonic yield is greatly improved by decreasing the driving laser wavelength from 800 nm to 400 nm. Appling the Perelomov-Popov-Terent’ev theory with the semiclassical cutoff law and one-dimensional time-dependent Schrödinger equation, the contribution of the Sn3+ ion to harmonic generation accounts for the cutoff extension at 400 nm. With the qualitative analysis of the phase mismatching effect, we reveal the phase matching caused by the dispersion of free electrons is greatly optimized in the 400 nm driving field relative to the 800 nm driving field. The high-order harmonic generated from laser-ablated tin plasma plumes driven by the short laser wavelength provides a promising way to extend cutoff energy and generate intensely coherent extreme ultraviolet radiation.

© 2023 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement

1. Introduction

High-order harmonic generation (HHG) driven by strong laser fields enables visible to infrared laser coherent up-conversion into the extreme ultraviolet region with ultrashort-time characteristics [13]. This technology is being widely used in attosecond scientific applications [4,5]. Over the decades, atoms and molecules in gas [69] have been the most common medium for HHG. To broaden the studied atomic species, laser-ablated plasma plumes (LPPs) are used as an alternative medium [10,11]. With the advantage of the resonant characteristics of special electronic structures in metal ions [1214], the high-order harmonic spectra generated by some metal ions in LPPs can appear obvious resonance enhancement [1519]. However, the harmonic cutoff of the high-order harmonics driven by LPPs is low, which seriously restricts the practical application of HHG from LPPs. How to improve the harmonic cutoff of LPPs without reducing the harmonic yield has always been a topic of great concern.

The basic process of the high-order harmonics generated by the low-density LPPs can be regarded as a quantum nonlinearity originating from atoms and ions, which is similar to the three-step model of gaseous atoms [20,21]. In the three-step model, the maximum energy of the radiated photon follows the cutoff law hνmax = Ip + 3.17Up, where the ponderomotive energy Up is proportional to the square of laser wavelength λ and the laser intensity I, Ip is the ionization potential of the particles. In the gaseous HHG, the extension of the harmonic cutoff has been achieved with great success by increasing the available laser wavelength λ [1,22,23] and the effective laser intensity I [2426]. For LPPs, many reports have also used laser wavelengths at 1.3-1.8 μm instead of 0.8 μm to generate high-order harmonics [2733]. Some experiments successfully extended the harmonic cutoff in carbon LPPs [27,30], accompanied by efficient harmonic generation [30], whereas others failed in extension of harmonic cutoff [28,29,3133]. This means that using a long-wavelength laser to extend harmonic cutoff is not easy for HHG in LPPs. Since the plasma itself contains a lot of electrons, it is almost impossible to achieve phase matching by suppressing the ionization rate like gaseous HHG. Meanwhile, the scaling of single atom response λ-(5∼6) [34] may result in a low harmonic conversion efficiency, which also makes the measurement of harmonic cutoff arduously. An alternative method of using higher ionization potential to extend harmonic cutoff has attracted extensive attentions [3539]. In the HHG experiments of manganese [38], vanadium [39] and titanium [37] LPPs, the third ionization potential was used to successfully extend the cutoff. However, further improving the ionization potential and solving the severe phase mismatch caused by free electron dispersion will become a challenge. Moreover, the harmonic conversion efficiency of these materials is relatively low [40,41], which limits their practical application. It is urgent to study a more suitable and convenient method from LPPs to extend harmonic cutoff and increase the harmonic yield at the same time.

In this work, we experimentally and theoretically investigate the high-order harmonic spectra from the laser-ablated tin plasma plumes (Sn-LPPs) at different laser wavelengths. The experimental results show that the highest observable harmonic cutoff at 800 nm laser driving wavelength is ∼51 eV (33rd), while it can be extended to ∼84 eV (27th) at 400 nm with a great improvement of the harmonic yield at the same time. By using the Perelomov-Popov-Terent’ev model [42] with the semiclassical cutoff law and one-dimensional time-dependent Schrödinger equation, the contribution of the Sn3+ ion to harmonic generation is responsible for the cutoff extension at 400 nm. In addition, we qualitatively analyze the improvement of phase matching caused by the dispersion of free electrons in the 400 nm driving field relative to the 800 nm driving field. And the dependence of harmonic cutoff in a 400 nm driving field on the intensity of driving pulses demonstrates the robustness of our theoretical calculation.

2. Experimental and numerical methods

2.1 Experimental design

The homebuilt HHG setup employed in the present work is shown in Fig. 1. Two laser beams are split from a commercial 1kHz, 0.8 μm Ti: sapphire amplifier system (Spectra Physics: Sprifire Ace). One 210 ps, 0.5 mJ laser beam is split from the amplified laser beam before time compression as the heating pulse (HP), and the other is temporally compressed to derive a 35fs, 5.5 mJ laser beam as the driving pulse (DP). HP is focused on the Sn sample surface by a 200 mm lens to generate the plasma plumes. The second harmonic (centered at 400 nm) is generated by a 0.5-mm-thick β-Barium borate (BBO) crystal with a conversion efficiency of ∼25% and separated from the fundamental pulses by two dichroic mirrors (DM). The half-wave plate (HWP) rotates the second harmonic to horizontal polarization. After the plasma plumes ablated by HP with a time delay of ∼50 ns, the horizontally polarized 400 nm laser beam served as DP is focused into Sn-LPPs through a spherical lens with a focal length of 300 mm to generate high-order harmonics. After passing through a narrow slit, the harmonics are reflected by a concave mirror onto a 1200 grooves/mm flat field grating, and then the dispersed harmonics are detected by a microchannel plate with a phosphor screen and recorded by a CCD camera. The integration time of the CCD camera is fixed at 200 ms. The intensity of each harmonic spectrum in this paper is related to the photon flux. The pulse width of DP at the location where DP interacted with the plasma plumes is estimated to be ∼50 fs due to the propagation of the optical path through the air.

 figure: Fig. 1.

Fig. 1. Schematic diagram of the experimental setup.

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2.2 Simulation methods

The Perelomov-Popov-Terent’ev (PPT) theory [42] is applicable not only for noble gases [43], but also for metals [4446]. In atomic units, the total rate of PPT ionization is

$${w_{PPT}}(F,\omega ) = \sum\limits_{q \ge {q_{\min }}}^\infty {{w_q}(F,\omega )} $$
where qmin is equal to (Ip + Up)/ω, which represents the minimum number of photons required to reach the effective ionization potential Ip + Up, and ω and F are the frequency and amplitude of the laser field, respectively. The rate of PPT ionization can be also written as
$$\begin{array}{c} {w_{PPT}}(F,\omega ) = \frac{{{\textrm{2}^{\textrm{2}{n^\ast }}}}}{{{n^\ast }\Gamma ({n^\ast } + {l^\ast } + 1)\Gamma ({n^\ast } - {l^\ast })}}\frac{{(2l + 1)(l + |m|)!}}{{{2^{|m|}}(|m|)!(l - |m|)!}}{I_p}{(\frac{{2{F_0}}}{F})^{2{n^\ast } - |m|- 1}}\\ \times {(1 + {\gamma ^2})^{|m|/2 + 3/4}}{A_m}(\omega ,\gamma )\exp [ - \frac{{2{F_0}}}{{3F}}g(\gamma )] \end{array}$$
with
$$\begin{aligned} g(\gamma ) &= \frac{\textrm{3}}{{\textrm{2}\gamma }}[(1 + \frac{1}{{\textrm{2}{\gamma ^2}}}){\sinh ^{ - 1}}\gamma - \frac{{\sqrt {1 + {\gamma ^2}} }}{{2\gamma }}],\\ {A_m}(F,\omega ) &= \frac{{\textrm{4}{\gamma ^2}}}{{\sqrt {3\pi } |m|!(1 + {\gamma ^2})}}\\ &\quad \times \sum\limits_{q \ge {q_{\min }}}^\infty {{e^{ - \alpha (\gamma )(q - v)}}{\omega _m}(\sqrt {\beta (\gamma )(q - {q_{\min }})} )} ,\\ {\omega _m}(x) &= \frac{{{x^{2|m|+ 1}}}}{2}\int_0^1 {\frac{{{e^{ - {x^2}t}}{t^{|m|}}}}{{\sqrt {1 - t} }}dt,} \\ \alpha (\gamma ) &= 2({\sinh ^{ - 1}}\gamma - \frac{\gamma }{{\sqrt {1 + {\gamma ^2}} }}),\\ \beta (\gamma ) &= \frac{{2\gamma }}{{\sqrt {1 + {\gamma ^2}} }}, \end{aligned}$$
where l and m are the orbital and magnetic quantum number of Sn ions, F0 = (2Ip)3/2 is the Coulomb field, γ is the Keldysh parameter, $\mathrm{\Gamma }(x )$ is the gamma function, ${n^\ast } = Z/\sqrt {2{I_p}} $ is the effective quantum number, ${l^\ast } = {n^\ast } - 1$ is the effective orbital quantum number. Here, Z is the charge of Sn ions after absorbing q photons. The direction of laser polarization determines the quantization axis.

In the duration of the laser pulse, the ionization probability of Sn ions can be calculated from the PPT ionization rate by integration

$$P = 1 - \exp [ - \int_{ - \infty }^{ + \infty } {w({F_0}(t))dt} ]$$
where F0(t) is a sine-squared envelope of the laser pulse, and the full width at half maximum (FWHM) of the envelope is the actual laser duration in our experiment. For each ionic species, the ionization probability is calculated as a function of the laser intensity, as shown in Fig. 4(a) and Fig. 4(c).

We also calculate the high-order harmonic spectra from different Sn ions by one-dimensional time-dependent Schrödinger equation (1D-TDSE). In length gauge for this system, the corresponding 1D-TDSE, in atomic units, is given by

$$i\frac{\partial }{{\partial t}}\psi (x,t) = [ - \frac{1}{2}\frac{{{\partial ^2}}}{{\partial {x^2}}} + V(x) + E(t) \cdot x]\textrm{ }\psi (x,t)$$

By utilizing the split operator method [47], we are able to solve the 1D-TDSE in Eq. (4). To prevent the wave packet from being unphysical reflected off the boundary, a mask function of the kind cos1/8 was employed. For the atomic potential function, a soft Coulomb function $V(x) ={-} Z/\sqrt {{x^2} + a}$ is utilized to prevent numerical inaccuracy brought on by the screening potential approaching the origin. Then, using Ehrenfest's theorem, the time-dependent induced dipole moment may be calculated as follows:

$$a(t) = \frac{{{\partial ^2}}}{{\partial {t^2}}}\left\langle {\psi \textrm{(}x,t\textrm{)}|x |\psi \textrm{(}x,t\textrm{)}} \right\rangle = \left\langle {\psi \textrm{(}x,t\textrm{)}\left|{ - \frac{{dV(x)}}{{dx}} - E(t)} \right|\psi \textrm{(}x,t\textrm{)}} \right\rangle $$

From the absolute square of the Fourier transformation of the time-dependent dipole accelerations, we may get the HHG power spectrum

$$P(\omega ) = {\left|{\int {{e^{ - i\omega t}}a(t)dt} } \right|^2}$$

3. Results and discussion

The harmonic spectra driven by the 400 nm laser field at different HP intensities are measured first to optimize the harmonic generation condition, as shown in Fig. 2. Clearly, the harmonic cutoff at the HP intensity from 0.8 × 1010 W/cm2 to 1.4 × 1010 W/cm2 is about 17th, 23rd, 27th and 23rd order, respectively. This non-monotonic trend indicates that the harmonic cutoff value is influenced by the density of LPPs, which is related to the HP intensity. The cutoff value reaches a maximum of 27 at the HP intensity of 1.2 × 1010 W/cm2. As the HP intensity increases, the background noise caused by plasma line emissions becomes more prominent. The cutoff begins to get lower at the intensity of 1.4 × 1010 W/cm2. The harmonic spectra as a function of HP intensity are also measured in the driving field of 800 nm. It is found that the HP intensity of 1.2×1010 W/cm2 is sufficient to give satisfactory harmonic spectrum in the driving fields of 400 nm and 800 nm without noticeable plasma emissions. Throughout the paper, we use a constant HP intensity at 1.2 × 1010 W/cm2. As shown in Fig. 2, we further observe a satellite peak on the right side of the 7th harmonic at 23.2 eV in the 400 nm driving field. This is most likely due to the second-order diffraction of the 15th harmonic [48,49]. And the 9th harmonic enhancement in all spectra is caused by the strong radiative transition of Sn2+ ion from 4d105s5p to 4d95s5p2, which has been verified well in the theoretical calculation [50].

 figure: Fig. 2.

Fig. 2. High-order harmonic spectra generated from Sn-LPPs in the 400 nm driving field with HP intensity at (a) 0.8 × 1010 W/cm2, (b) 1 × 1010 W/cm2, (c) 1.2 × 1010 W/cm2, (d) 1.4 × 1010 W/cm2, respectively. The DP intensity is maintained at 8 × 1014 W/cm2 for all the spectra.

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Figure 3 shows the harmonic spectra in the driving fields of 800 nm and 400 nm, respectively. In the 800 nm driving field, the 17th harmonic has a higher yield than the neighboring harmonics. This enhancement can be identified as the transition between two Sn+ ionic states (4d105s25p and 4d95s25p2) with a frequency (26.22 eV) close to the 17th harmonic [51]. To achieve higher cutoff energy and have comparability at different laser wavelengths in the harmonic spectrum, the same camera integration time and gain factor are used in the measurement. Most notably, the harmonic cutoff in the 800 nm driving field is much higher than the previous reports [15,48], being about the 33rd order (∼51 eV). And the cutoff in the 400 nm driving field can be further extended to around the 27th order (∼84 eV). Interestingly, the cutoff energy is increased at short wavelengths, in contrast to what is expected from the three-step model in gaseous HHG according to the semiclassical cutoff law. Moreover, the harmonic yield is also much improved at short wavelengths. We can observe that the harmonic yield of the 15th harmonic (∼46 eV) in the driving field of 400 nm almost surpasses that of the 29th harmonic (∼45 eV) in the driving field of 800 nm by 16 times. It is known that the conversion efficiency is the ratio of harmonic power to the laser power (photon energy × photon flux/ laser power) [52]. In this experiment, the actual single pulse energies of 400 nm and 800 nm lasers are 350 μJ and 1600 μJ, respectively. Therefore, the actual harmonic conversion efficiency at 400 nm is 70 times higher than that at 800 nm, which is similar to the single-atom response (25-6 times) [34].

 figure: Fig. 3.

Fig. 3. High-order harmonic spectra generated from Sn-LPPs driven by (a) 800 nm laser field with DP intensity at 9 × 1014 W/cm2, and (b) 400 nm laser field with DP intensity at 8 × 1014 W/cm2. The HP intensity is maintained at 1.2 × 1010 W/cm2 for all the spectra. The purpose of choosing DP with different intensities is to measure the maximum cutoff energy at different driving wavelengths.

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To further investigate the inverse relationship between the harmonic cutoff and laser wavelength in Sn-LPPs HHG, the PPT model with the semiclassical cutoff law and 1D-TDSE methods are applied to distinguish the influenced factors in the microscopic particles, as shown in Fig. 4. Based on the physical picture of the three-step model, due to the depletion of the ground state (i.e. ionization probability reaches 99.9%), the harmonic cutoff energy cannot be further increased before the laser pulse reaches the peak intensity. The maximum value of the effective laser intensity is defined as the saturation intensity Isat. To quantitatively describe the ionization process driven by 800 and 400 nm laser fields, the PPT theory is applied to estimate the Isat of different Sn ions. Figure 4(a) shows the Sn ion yields as the function of DP intensity with 400 nm driving laser wavelength. The ionization probabilities of Sn+, Sn2+ and Sn3+ in a 400 nm driving field are saturated (i.e. 99.9%) at the intensities of 0.09 × 1014 W/cm2, 4.07 × 1014 W/cm2 and 8.33 × 1014 W/cm2, respectively. According to the semiclassical cutoff law, the harmonic cutoff of Sn3+ at the saturation intensity is estimated to be the 25th harmonic, which is close to our experimental cutoff value. Therefore, the contribution of the Sn3+ ion to harmonic generation is responsible for the extended harmonic cutoff of Sn-LPPs HHG driven by a 400 nm laser field. This assignment can be further confirmed by the method of 1D-TDSE as shown in Fig. 4(b). We summarize the cutoff energy obtained theoretically in Table 1. The results of the theoretical analysis are in good agreement with our experimental findings in a 400 nm laser field.

 figure: Fig. 4.

Fig. 4. Calculated ionization probabilities of different Sn ions as a function of DP intensity in (a) 400 nm, and (c) 800 nm laser fields. The saturation intensities Isat of each particle is depicted by the vertical dash line. (b) and (d) show the calculated high-order harmonic spectra generated from Sn2+ and Sn3+ particles at each saturation intensity in 400 nm and 800 nm laser fields, respectively. The dashed lines represent the calculated harmonic cutoff, which is judged on the position of the sharp decrease in the harmonic intensity after a primary plateau.

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Tables Icon

Table 1. Calculated cutoff values in 400 and 800 nm driving fields from different ions using a semiclassical model and 1D-TDSE

Driven by 800 nm laser wavelength, the Sn3+ ion yield exceeds 90% at the experimental laser intensity of 9 × 1014 W/cm2 as shown in Fig. 4(c). It appears that the ionization of Sn3+ may be contributed to the harmonic spectrum generated by the 800 nm laser field. However, the theoretically predicted cutoff from Sn3+ at its saturation intensity is much higher than our experimental result and the previous measurements [15,48]. This is mainly due to the above theories without taking the macroscopical propagation effect into account. To achieve effective frequency up-conversion and optimize cutoff, the generated harmonic photons need to have the same phase velocity as the driving field, i.e., the phase matching. The phase mismatching term Δk is a sum of contributions from the dispersion terms of atoms/ions, free electrons, quantum phase Δkint, and laser geometry ΔkG. Although the focusing lens of DP is only 300 mm in our experiment, a few millimeters of Rayleigh length is still much longer than the plasma length of a hundred microns, which will cause the term ΔkG to be neglected [5355]. For the term Δkint, it is a function of ΔI/Δz, and within the Rayleigh length, the change in DP intensity ΔI near the plasma length Δz is very small [53,54]. Therefore, in comparison with the dispersion terms of atoms/ions and electrons, for Sn-LPPs HHG, the contributions of ΔkG and Δkint to the phase mismatching are negligible [17,55]. To analyze the phase mismatching of Sn-LPPs HHG at different laser wavelengths, the term Δk can be simplified as

$$\triangle k = q{k_\omega } - {k_{q\omega }} \approx{-} \underbrace{{\frac{{{n_i}{\omega _q}}}{c}(\delta + \Delta \delta )}}_{{atom\textrm{ and ions}}} + \underbrace{{\frac{{{\omega _q}{n_e}{e^2}}}{{c{\varepsilon _0}m\omega _{DP}^2}}}}_{{free\textrm{ electrons}}}$$
where ωq is the qth harmonic frequency, ωDP is the DP frequency, ε0 is the vacuum permittivity, m is the electron mass, δ is the refractive index difference between DP and the harmonic from different ions, Δδ is the nonlinear refractive index from different ions, ni is the density of different particles of Sn and i=0 denotes atoms, i=1, 2, 3… denote ions with different charges, respectively. In a multi-species plasma medium, the free electron term plays a major role in the phase mismatching [17,55], whereas the atomic term is replaced by the linear dispersion and the Kerr effect of the ion to compensate for the electronic dispersion term and achieve phase matching. It has been demonstrated that the dispersion of ions is negative and increases with laser frequency ωDP [55]. The free electron term is positive and inversely proportional to the square of laser frequency ωDP, therefore, the perfect agreement between theory and experiment in the 400 nm driving field is due to the improvement of phase matching in the 400 nm driving field compared with the 800 nm driving field.

Figure 5 shows the harmonic cutoff as a function of DP intensity in the 400 nm driving field. There is a small plateau at the 15th order, and the cutoff value remains constant after reaching the 27th order. According to the PPT theory, the ionization process has a window where the Sn2+ yield is saturated and the Sn3+ ions cannot achieve effective ionization within the intensity ranges from 3.99 × 1014 W/cm2 to 4.62 × 1014 W/cm2. The cutoff will be the same in this intensity region, thus, the first cutoff plateau is derived from the contribution of the Sn2+ ion to harmonic generation. In the same way, the second cutoff plateau at the 27th order corresponds to the contribution of the Sn3+ ion to harmonic generation. However, the ionization of the Sn4+ ion needs the peak laser intensity to reach 3 × 1015 W/cm2, which is a harsh experimental condition. Therefore, the cutoff value remains constant at the intensity ranges from 8 × 1014 W/cm2 to 1.4 × 1015 W/cm2.

 figure: Fig. 5.

Fig. 5. Dependence of the harmonic cutoff in the 400 nm driving field on DP intensity.

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4. Conclusion

In summary, we have studied the high-order harmonic spectra of Sn-LPPs in 800 and 400 nm driving fields. Experimental measurement shows a simultaneous enhancement of the harmonic cutoff and the harmonic yield at the short laser wavelength. This enhancement in synchronization has not been achieved in previous HHG experiments of LPPs. Theoretical calculations are in good agreement with our result in the 400 nm driving field, which confirms that the contribution of the Sn3+ ion to harmonic generation accounts for the cutoff extension at 400 nm. Considering the propagation effect in experimental measurements, we reveal the phase matching caused by the dispersion of free electrons is much improved in the 400 nm driving field relative to the 800 nm driving field. Two cutoff plateaus in dependence with DP intensity at 400 nm laser wavelength can also be well described by our theories even without consideration of the phase matching effect, clarifying the robustness of our theoretical calculation. We prove that the high-order harmonic generated from laser-ablated tin plasma plumes driven by a short laser wavelength effectively extends the cutoff energy and generates intensely coherent extreme ultraviolet radiation.

Funding

National Natural Science Foundation of China (62121005, 62134009); Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences; Department of Science and Technology of Jilin Province (YDZJ202102CXJD002).

Acknowledgments

We thank Dianxiang Ren and Yu Hang Lai for interesting discussions.

Disclosures

The authors declare no competing financial interest.

Data availability

Data underlying the results presented in this paper are not publicly available at this time but may be obtained from the authors upon reasonable request.

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Data availability

Data underlying the results presented in this paper are not publicly available at this time but may be obtained from the authors upon reasonable request.

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Figures (5)

Fig. 1.
Fig. 1. Schematic diagram of the experimental setup.
Fig. 2.
Fig. 2. High-order harmonic spectra generated from Sn-LPPs in the 400 nm driving field with HP intensity at (a) 0.8 × 1010 W/cm2, (b) 1 × 1010 W/cm2, (c) 1.2 × 1010 W/cm2, (d) 1.4 × 1010 W/cm2, respectively. The DP intensity is maintained at 8 × 1014 W/cm2 for all the spectra.
Fig. 3.
Fig. 3. High-order harmonic spectra generated from Sn-LPPs driven by (a) 800 nm laser field with DP intensity at 9 × 1014 W/cm2, and (b) 400 nm laser field with DP intensity at 8 × 1014 W/cm2. The HP intensity is maintained at 1.2 × 1010 W/cm2 for all the spectra. The purpose of choosing DP with different intensities is to measure the maximum cutoff energy at different driving wavelengths.
Fig. 4.
Fig. 4. Calculated ionization probabilities of different Sn ions as a function of DP intensity in (a) 400 nm, and (c) 800 nm laser fields. The saturation intensities Isat of each particle is depicted by the vertical dash line. (b) and (d) show the calculated high-order harmonic spectra generated from Sn2+ and Sn3+ particles at each saturation intensity in 400 nm and 800 nm laser fields, respectively. The dashed lines represent the calculated harmonic cutoff, which is judged on the position of the sharp decrease in the harmonic intensity after a primary plateau.
Fig. 5.
Fig. 5. Dependence of the harmonic cutoff in the 400 nm driving field on DP intensity.

Tables (1)

Tables Icon

Table 1. Calculated cutoff values in 400 and 800 nm driving fields from different ions using a semiclassical model and 1D-TDSE

Equations (8)

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w P P T ( F , ω ) = q q min w q ( F , ω )
w P P T ( F , ω ) = 2 2 n n Γ ( n + l + 1 ) Γ ( n l ) ( 2 l + 1 ) ( l + | m | ) ! 2 | m | ( | m | ) ! ( l | m | ) ! I p ( 2 F 0 F ) 2 n | m | 1 × ( 1 + γ 2 ) | m | / 2 + 3 / 4 A m ( ω , γ ) exp [ 2 F 0 3 F g ( γ ) ]
g ( γ ) = 3 2 γ [ ( 1 + 1 2 γ 2 ) sinh 1 γ 1 + γ 2 2 γ ] , A m ( F , ω ) = 4 γ 2 3 π | m | ! ( 1 + γ 2 ) × q q min e α ( γ ) ( q v ) ω m ( β ( γ ) ( q q min ) ) , ω m ( x ) = x 2 | m | + 1 2 0 1 e x 2 t t | m | 1 t d t , α ( γ ) = 2 ( sinh 1 γ γ 1 + γ 2 ) , β ( γ ) = 2 γ 1 + γ 2 ,
P = 1 exp [ + w ( F 0 ( t ) ) d t ]
i t ψ ( x , t ) = [ 1 2 2 x 2 + V ( x ) + E ( t ) x ]   ψ ( x , t )
a ( t ) = 2 t 2 ψ ( x , t ) | x | ψ ( x , t ) = ψ ( x , t ) | d V ( x ) d x E ( t ) | ψ ( x , t )
P ( ω ) = | e i ω t a ( t ) d t | 2
k = q k ω k q ω n i ω q c ( δ + Δ δ ) a t o m  and ions + ω q n e e 2 c ε 0 m ω D P 2 f r e e  electrons
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