化学
电子转移
半导体
化学物理
分子
动能
纳米技术
电子
光化学
材料科学
有机化学
光电子学
量子力学
物理
作者
Ke Hu,Amber D. Blair,Eric J. Piechota,Phil A. Schauer,Renato N. Sampaio,Fraser G. L. Parlane,Gerald J. Meyer,Curtis P. Berlinguette
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2016-06-20
卷期号:8 (9): 853-859
被引量:102
摘要
Molecular approaches to solar-energy conversion require a kinetic optimization of light-induced electron-transfer reactions. At molecular-semiconductor interfaces, this optimization has previously been accomplished through control of the distance between the semiconductor donor and the molecular acceptor and/or the free energy that accompanies electron transfer. Here we show that a kinetic pathway for electron transfer from a semiconductor to a molecular acceptor also exists and provides an alternative method for the control of interfacial kinetics. The pathway was identified by the rational design of molecules in which the distance and the driving force were held near parity and only the geometric torsion about a xylyl- or phenylthiophene bridge was varied. Electronic coupling through the phenyl bridge was a factor of ten greater than that through the xylyl bridge. Comparative studies revealed a significant bridge dependence for electron transfer that could not be rationalized by a change in distance or driving force. Instead, the data indicate an interfacial electron-transfer pathway that utilizes the aromatic bridge orbitals.
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