Resonance energy transfer, motional narrowing, and vibrational dephasing in molecular crystals: 390 cm−1 internal vibration of naphthalene
- 15 January 1983
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 78 (2) , 626-631
- https://doi.org/10.1063/1.444818
Abstract
For the naphthalene‐h8 crystal, the vibrational dephasing of the 390 cm−1 Raman active vibration is investigated by the temperature dependence of the linewidth and the line shape in the Raman spectra. This mode shows a relatively large resonance transfer interaction with a consequent factor group splitting of ∼5.5 cm−1. The corresponding transition in the isotopic mixed crystal, composed of 10% naphthalene‐h8 and 90% naphthalene‐d8, is, predominantly, due to the monomer. This monomer transition exhibits a Gaussian line shape at 4 K and has a width of ∼1.5 cm−1. In the neat naphthalene‐h8 crystal at 4 K, the line shape of the higher energy Davydov component is found to be a motionally narrowed Lorentzian with a width much smaller than that of the monomer transition in the isotopic mixed crystal. In contrast to this, the line shape of the lower energy Davydov component is asymmetric. The low energy side of the lower Davydov component is found to obey the Urbach rule, while its high energy side is a Lorentzian. Furthermore, the width of the lower Davydov component is larger than that of the upper Davydov component but still smaller than what is observed for the corresponding monomer transition in the isotopic mixed crystal. This result suggests that the vibrational exciton band k‐scattering mechanism, which involves the exciton–phonon scattering, does not contribute significantly to the vibrational dephasing. It is because such a mechanism predicts that at 4 K the upper Davydov component would be broader than the lower Davydov component as observed for the electronic excitons in molecular crystals. A detailed study of temperature dependence of the linewidth of the upper Davydov component also supports the assumption that the k scattering within the vibrational exciton band is not the main contributor to the dephasing of the 390 cm−1 vibration. This observed temperature dependence of the linewidth is found to be consistent with the mechanism of pure dephasing which involves an off‐diagonal quartic anharmonic interaction with the high‐frequency in‐plane librational phonon motions.Keywords
This publication has 30 references indexed in Scilit:
- Dephasing of optical phonons in a substitutionally disordered organic solid. The lowest-frequency Raman-active phonon of a binary solid solution between p-bromochlorobenzene and p-dichlorobenzeneThe Journal of Physical Chemistry, 1982
- Dephasing times and linewidths of optical transitions in molecular crystals. Temperature dependence of line shapes, linewidths, and frequencies of Raman active phonons in naphthaleneThe Journal of Chemical Physics, 1979
- The origin of vibrational dephasing of polyatomic molecules in condensed phasesThe Journal of Chemical Physics, 1979
- Effects of Energy Exchange on Vibrational Dephasing Times in Raman ScatteringPhysical Review Letters, 1977
- Phonon scattering and exciton linewidths in naphthalene and phenanthrene molecular crystalsJournal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics, 1977
- Vibrational, torsional, and librational excitons in molecular crystals: Raman spectra of neat and isotopic mixed dureneThe Journal of Chemical Physics, 1973
- Method of Heavily Doped Isotopic Mixed Crystal for Determination of Exciton Splittings and Normal Modes: Raman Spectra of NaphthaleneThe Journal of Chemical Physics, 1972
- Vibrational Exciton Density of States in Solid BenzeneThe Journal of Chemical Physics, 1970
- Benzene Vibrational Exciton SpectrumThe Journal of Chemical Physics, 1967
- Scattering of Neutrons by an Anharmonic CrystalPhysical Review B, 1962