Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Chemical Physics Letters

Photon-echo decay of naphthalene in durene and perdeutero-naphthalene

Thys J. Aartsma, Douwe A. Wiersma

Published Mar 1, 1978• 20 citations
Publisher
DOI
10.1016/0009-2614(78)85251-8

Related papers

A photon echo study of pentacene in naphthalene at high pressure

Robert A. Crowell, Eric L. Chronister

Chemical Physics Letters•Dec 1, 1993•9 citations

Optical density effects in photon echo experiments

Radley W. Olson, Howard W. H. Lee, Frank G. Patterson +1 more

The effects of optical density (OD) on photon echo experiments is examined both theoretically and experimentally. The theoretical treatment involves coupled Maxwell-Optical Bloch equations, and the experiments are picosecond photon echo studies of the mixed molecular crystal, pentacene in naphthalene. Under high power excitation (π/2, π) in high OD samples, the echo decays are predicted and observed to be faster than decays arising solely from the intrinsic molecular T2. The increase in the echo decay rate vanishes in the limit of low power or low OD, permitting the intrinsic molecular T2 to be measured. Previously reported concentration effects are shown to actually be optical density effects. The experimentally determined intrinsic molecular T2 of pentacene in naphthalene is shown to be independent of concentration and temperature (below ∼2 K) and T2≠2T1. It is suggested that the difference between T2 and 2T1 is due to the static multiplet level structure arising from the electronic state-phonon coupling.

The Journal of Chemical Physics•Jan 1, 1982•79 citations

Stimulated photon echo decay arising from spectral diffusion in GaSe

南不二雄, F. Minami

•Jan 1, 1999•0 citations

Photon Echo of Pentacene Molecules Introduced in Crystals with High Concentration

Yuzo Yoshikuni, Arao Nakamura, Shigeo Shionoya

Abstract Photon echo decay time is measured for pentacence molecules introduced in naphthalene and p-terphenyl crystals with rather high concentrations (10−6–105 mol/mol) at temperatures between 1.6 K and 4.1 K, using a tunable picosecond laser system consisting of a mode-locked YAG laser and a parametric oscillator. In naphthalene echo decay time increases with lowering temperature approaching a constant value below 2 K, but in p-terphenyl it is almost constant. The phase relaxation time at very low temperature is much shorter than twice the population relaxation time in both crystals, indicating that pure dephasing processes exist. Analyzing the results it turns out that there exsists a pure dephasing process which is temperature-independent and is very probably due to interactions between pentacene molecules, in addition to the temperature-dependent dephasing process due to the scattering of pseudolocalized phonons.

Bulletin of the Chemical Society of Japan•Sep 1, 1982•5 citations

Optical free induction decay of molecules undergoing radiative and radiationless relaxation

Harmen de Vries, Douwe A. Wiersma

In this paper we examine the effect of radiative and radiationless processes on optical free induction decay (OFID) in singlet–singlet transitions of molecules in the condensed phase. The main conclusion is that the applicability of OFID to molecular singlet–singlet transitions is severely limited by the presence of an intermediate triplet state, which quite often forms a bottleneck in the optical pumping cycle. Using the theoretically derived formulas for the OFID signal, we examine the feasibility of OFID experiments on the mixed crystals of porphin in n-octane and naphthalene in durene and conclude that such experiments, if at all fruitful, would be difficult to execute. We re-evaluate the reported OFID results of pentacene in p-terphenyl and obtain for the lowest 1B2u←1A1g transition a dipole moment of 0.9±0.3 D.

The Journal of Chemical Physics•Jul 15, 1978•27 citations

Stimulated photon echo decay arising from spectral diffusion in GaSe

Takashi Kuroda

•Jan 1, 1999•0 citations
The effects of optical density (OD) on photon echo experiments is examined both theoretically and experimentally. The theoretical treatment involves coupled Maxwell-Optical Bloch equations, and the experiments are picosecond photon echo studies of the mixed molecular crystal, pentacene in naphthalene. Under high power excitation (π/2, π) in high OD samples, the echo decays are predicted and observed to be faster than decays arising solely from the intrinsic molecular T2. The increase in the echo decay rate vanishes in the limit of low power or low OD, permitting the intrinsic molecular T2 to be measured. Previously reported concentration effects are shown to actually be optical density effects. The experimentally determined intrinsic molecular T2 of pentacene in naphthalene is shown to be independent of concentration and temperature (below ∼2 K) and T2≠2T1. It is suggested that the difference between T2 and 2T1 is due to the static multiplet level structure arising from the electronic state-phonon coupling.
Abstract Photon echo decay time is measured for pentacence molecules introduced in naphthalene and p-terphenyl crystals with rather high concentrations (10−6–105 mol/mol) at temperatures between 1.6 K and 4.1 K, using a tunable picosecond laser system consisting of a mode-locked YAG laser and a parametric oscillator. In naphthalene echo decay time increases with lowering temperature approaching a constant value below 2 K, but in p-terphenyl it is almost constant. The phase relaxation time at very low temperature is much shorter than twice the population relaxation time in both crystals, indicating that pure dephasing processes exist. Analyzing the results it turns out that there exsists a pure dephasing process which is temperature-independent and is very probably due to interactions between pentacene molecules, in addition to the temperature-dependent dephasing process due to the scattering of pseudolocalized phonons.
In this paper we examine the effect of radiative and radiationless processes on optical free induction decay (OFID) in singlet–singlet transitions of molecules in the condensed phase. The main conclusion is that the applicability of OFID to molecular singlet–singlet transitions is severely limited by the presence of an intermediate triplet state, which quite often forms a bottleneck in the optical pumping cycle. Using the theoretically derived formulas for the OFID signal, we examine the feasibility of OFID experiments on the mixed crystals of porphin in n-octane and naphthalene in durene and conclude that such experiments, if at all fruitful, would be difficult to execute. We re-evaluate the reported OFID results of pentacene in p-terphenyl and obtain for the lowest 1B2u←1A1g transition a dipole moment of 0.9±0.3 D.