THEORY OF ELECTRON-TRANSFER RATES ACROSS LIQUID LIQUID INTERFACES .2. RELATIONSHIPS AND APPLICATION

被引:126
|
作者
MARCUS, RA
机构
[1] A. A. Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena
来源
JOURNAL OF PHYSICAL CHEMISTRY | 1991年 / 95卷 / 05期
关键词
D O I
10.1021/j100158a023
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
In part 1 an expression was obtained for the exchange current rate constant k12II for an electron transfer between a reactant in one liquid and a second reactant in a second immiscible liquid, across an (assumed) sharp interfacial boundary. This expression is used to obtain a relation between k12II and the self-exchange rate constants k11 and k22 for electron transfer in homogeneous solutions, each redox species being in its respective liquid phase. The relation provides an extension of the "cross-relation" for one-phase electron transfer to this two-phase case. An expression is also given relating k12II to the usual metal-liquid electrochemical exchange current rate constants k1el and k2el, these k(el,)s referring to each reactant in its respective solvent phase. An alternative limiting model for the interfacial region is also considered, in which that region is now broad, instead of sharp. The results of both models are compared with the limited available kinetic data, and the desirability of further experimental studies is noted.
引用
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页码:2010 / 2013
页数:4
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