Charge recombination versus charge separation in donor-bridge-acceptor systems

被引：0

作者：

Wiberg, Joanna ^{[1
]}

Guo, Lijun ^{[1
,3
]}

Pettersson, Karin ^{[1
]}

Nilsson, Daniel ^{[2
]}

Ljungdahl, Thomas ^{[2
]}

Mårtensson, Jerker ^{[2
]}

Albinsson, Bo ^{[1
]}

机构：

[1] Department of Chemical and Biological Engineering/Physical Chemistry, Chalmers University of Technology, SE-412 96 Göteborg, Sweden

[2] Department of Organic Chemistry, Chalmers University of Technology, SE-412 96 Göteborg, Sweden

[3] Physics Department, Henan University, Kaifeng 475001, China

来源：

Journal of the American Chemical Society | 2007年 / 129卷 / 01期

关键词：

Optimizing the ratio of the rates for charge separation (CS) over charge recombination (CR) is crucial to create long-lived charge-separated states. Mastering the factors that govern the electron transfer (ET) rates is essential when trying to achieve molecular-scale electronics; artificial photosynthesis; and also for the further development of solar cells. Much work has been put into the question of how the donor-acceptor distances and donor-bridge energy gaps affect the electronic coupling; VDA; and thus the rates of ET. We present here a unique comparison on how these factors differently influence the rates for CS and CR in a porphyrin-based donor-bridge-acceptor model system. Our system contains three series; each of which focuses on a separate charge-transfer rate-determining factor; the donor-acceptor distance; the donor-bridge energy gap; and last; the influence of the electron acceptor on the rate for charge transfer. In these three series both CS and CR are governed by superexchange interactions which make a CR/CS comparative study ideal. We show here that the exponential distance dependence increases slightly for CR compared to that for CS as a result of the increased tunneling barrier height for this reaction; in accordance with the McConnell superexchange model. We also show that the dependence on the tunneling barrier height is different for CS and CR. This difference is highly dependent on the electron acceptor and thus cannot solely be explained by the differences in the frontier orbitals of the electron donor in these porphyrin systems. © 2007 American Chemical Society;

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摘要：

Journal article (JA)

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页码：155 / 163