Development of kinetic analysis system in pump-probe measurement based on femtosecond chromium:: forsterite laser and its application to S1-S0 relaxation dynamics of azulene

被引:11
作者
Matsuda, H
Nagasawa, Y [1 ]
Miyasaka, H
Okada, T
机构
[1] Osaka Univ, Grad Sch Engn Sci, Dept Chem, Osaka 5608531, Japan
[2] Osaka Univ, Res Ctr Mat Sci Extreme Condit, Osaka 5608531, Japan
关键词
chromium : forsterite laser; femtosecond spectroscopy; azulene; ultrafast dynamics;
D O I
10.1016/S1010-6030(02)00407-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ultrafast transient absorption measurement system with cavity-dumped chromium:forsterite (Cr:F) laser as a light source was developed. The second harmonic of the Cr:F laser can cover the immeasurable region of the titanium: sapphire laser which is nowadays the most popular light source for the ultrafast spectroscopy. The second harmonic of the Cr:F laser was tunable from 620 to 640 nm and the shortest pulse duration attained in the present condition was similar to25 fs. The sensitivity of this laser to ultrafast spectroscopy was evaluated by the measurement of S-0 and S-1 state dynamics of azulene. In spite of extremely small molar extinction coefficient of the S-1 <-- S-0 transition, i.e. 300 M-1 cm(-1), the ultrafast dynamics of azulene after photo-excitation to S-1 state was clearly observed with high S/N ratio and <= 30 fs time resolution. Although the small molar extinction coefficient value of 300 M-1 cm(-1), pump-and-probe measurement clearly resolved the multi-exponential recovery profile with a very weak oscillation of 160 cm(-1). (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:69 / 75
页数:7
相关论文
共 38 条
[11]   THE NATURE OF SIMPLE PHOTODISSOCIATION REACTIONS IN LIQUIDS ON ULTRAFAST TIME SCALES [J].
HARRIS, AL ;
BROWN, JK ;
HARRIS, CB .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1988, 39 :341-366
[12]   SPECTRAL MANIFESTATIONS OF NONRADIATIVE PROCESSES IN AZULENE [J].
HOCHSTRASSER, RM ;
LI, TY .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1972, 41 (02) :297-+
[13]   PICOSECOND DYNAMICS OF AZULENE [J].
IPPEN, EP ;
SHANK, CV ;
WOERNER, RL .
CHEMICAL PHYSICS LETTERS, 1977, 46 (01) :20-23
[14]   CHARACTERIZATION OF ELECTRONIC TRANSITIONS IN COMPLEX MOLECULES [J].
KASHA, M .
DISCUSSIONS OF THE FARADAY SOCIETY, 1950, (09) :14-19
[15]   GEMINATE RECOMBINATION OF MOLECULAR-IODINE - THE ROLE OF A-STATE AND A'-STATES [J].
KELLEY, DF ;
ABULHAJ, NA ;
JANG, DJ .
JOURNAL OF CHEMICAL PHYSICS, 1984, 80 (09) :4105-4109
[16]   POTENTIAL SYMMETRY-BREAKING, STRUCTURE AND DEFINITE VIBRATIONAL ASSIGNMENT FOR AZULENE - MULTICONFIGURATIONAL AND DENSITY-FUNCTIONAL RESULTS [J].
KOZLOWSKI, PM ;
RAUHUT, G ;
PULAY, P .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (13) :5650-5661
[17]   EXCESS ENERGY-DEPENDENCE OF INTERNAL-CONVERSION IN THE S1 STATE OF AZULENE [J].
KULKARNI, SK ;
KENNY, JE .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (07) :4441-4443
[18]   Structure and vibrational spectrum of some polycyclic aromatic compounds studied by density functional theory .1. Naphthalene, azulene, phenanthrene, and anthracene [J].
Martin, JML ;
ElYazal, J ;
Francois, JP .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (38) :15358-15367
[19]   FEMTOSECOND VIBRATIONAL-RELAXATION MEASUREMENT OF AZULENE USING TEMPORALLY INCOHERENT-LIGHT [J].
MATSUMOTO, T ;
UEDA, K ;
TOMITA, M .
CHEMICAL PHYSICS LETTERS, 1992, 191 (06) :627-632
[20]   Ultrafast excited state deactivation of triphenylmethane dyes [J].
Nagasawa, Y ;
Ando, Y ;
Kataoka, D ;
Matsuda, H ;
Miyasaka, H ;
Nagasawa, Y .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (10) :2024-2035