Expand this Topic clickable element to expand a topic
Skip to content
Optica Publishing Group

Photochemical Hole Burning and Debye-Waller Factor in Polyvinylalcohol doped with Ionic Porphyrins

Not Accessible

Your library or personal account may give you access

Abstract

Photochemical holes can be burned at relatively high temperatures in the Qx band of a free base porphyrin with ionic substituents when the molecule is dispersed in polyvinylalcohol (PVA) [1-2]. This characteristics of the porphyrin-PVA system is due to the facts that the Debye-Waller factor is relatively large [3] and the thermally activated backward reaction is small [4], Figure 1(a) shows one of such porphyrin molecules, TCPP(Na). The large Debye-Waller factor in porphyrin-PVA system is a direct consequence of a high mean phonon frequency. The typical phonon energy of the porphyrin-PVA system, which was determined as the energy deference between the zero-phonon hole and the bottom of the side hole, is as large as 25 cm–1. According to ref. 3, the Debye-Waller factor f(T) of porphyrin-PVA system is well represented by one-phonon approximation.

© 1994 Optical Society of America

PDF Article
More Like This
Photochemical Hole Burning of Ionic Dye Molecules

K. Sakoda, K. Kominami, and M. Iwamoto
MGG5 OSA Annual Meeting (FIO) 1989

Photochemical Hole Burning of Organic Dye Doped in Inorganic Semiconductor: Zinc Porphyrin in Titanium Dioxide

Shinjiro Machida, Kazuyuki Horie, and Takashi Yamasita
WD49 Spectral Hole-Burning and Related Spectroscopies: Science and Applications (SHBL) 1994

Photochemical Hole Burning of Porphin-Cross-Linked Polymers

Masayuki Maeda and Kazuaki Sakoda
WD39 Spectral Hole-Burning and Related Spectroscopies: Science and Applications (SHBL) 1994

Select as filters


Select Topics Cancel
© Copyright 2024 | Optica Publishing Group. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies.