Mapping out the conduction band under CTTS transitions:: the photodetachment quantum yield of sodide (Na-) in tetrahydrofuran

被引:25
作者
Barthel, ER [1 ]
Schwartz, BJ [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0009-2614(03)00922-9
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
Upon photoexcitation of the charge-transfer-to-solvent absorption band of Na- in tetrahydrofuran (THF), electrons detach into immediate contact pairs, solvent-separated contact pairs, or as free electrons. In this Letter, we analyze the recombination dynamics of Na- at multiple excitation wavelengths to determine the action spectrum for production of each type of electron. The action spectra match well with the four Gaussian sub-bands (corresponding to three p-like CTTS states and the continuum) needed to describe the polarized bleach recovery. We also find that the Na- free-electron action spectrum is linearly related to the Rb-/THF photocurrent action spectrum measured by Levanon and co-workers. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:435 / 443
页数:9
相关论文
共 22 条
[1]   Direct observation of charge-transfer-to-solvent (CTTS) reactions:: Ultrafast dynamics of the photoexcited alkali metal anion sodide (Na-) [J].
Barthel, ER ;
Martini, IB ;
Schwartz, BJ .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (21) :9433-9444
[2]   Solvent effects on the ultrafast dynamics and spectroscopy of the charge-transfer-to-solvent reaction of sodide [J].
Barthel, ER ;
Martini, IB ;
Keszei, E ;
Schwartz, BJ .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (13) :5916-5931
[3]   How does the solvent control electron transfer? Experimental and theoretical studies of the simplest charge transfer reaction [J].
Barthel, ER ;
Martini, IB ;
Schwartz, BJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (49) :12230-12241
[4]   THEORY AND APPLICATIONS OF CHARGE-TRANSFER-TO-SOLVENT SPECTRA [J].
BLANDAMER, MJ ;
FOX, MF .
CHEMICAL REVIEWS, 1970, 70 (01) :59-+
[5]   Excited states of iodide anions in water: A comparison of the electronic structure in clusters and in bulk solution [J].
Bradforth, SE ;
Jungwirth, P .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (07) :1286-1298
[6]   Reply to the comment on 'Iodine effect on the relaxation pathway of photoexcited I-(H2O)n clusters' [Chem. Phys. Lett. 335 (2001) 475] [J].
Chen, HY ;
Sheu, WS .
CHEMICAL PHYSICS LETTERS, 2002, 353 (5-6) :459-462
[8]   Optical absorption and reflection spectra of Na+(C222)Na- [J].
Hendrickson, JE ;
Pratt, WP ;
Kuo, CT ;
Xie, QS ;
Dye, JL .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (09) :3395-3401
[9]   Time-resolved scavenging and recombination dynamics from l:e- caged pairs [J].
Kloepfer, JA ;
Vilchiz, VH ;
Lenchenkov, VA ;
Chen, XY ;
Bradforth, SE .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (02) :766-778
[10]   Mechanisms of the ultrafast production and recombination of solvated electrons in weakly polar fluids:: Comparison of multiphoton ionization and detachment via the charge-transfer-to-solvent transition of Na- in THF [J].
Martini, IB ;
Barthel, ER ;
Schwartz, BJ .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (24) :11245-11257