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Volumn 112, Issue 7, 2000, Pages 3358-3369

On the theory of electron transfer reactions at semiconductor electrode/liquid interfaces

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EID: 0000262396     PISSN: 00219606     EISSN: None     Source Type: Journal    
DOI: 10.1063/1.480918     Document Type: Article
Times cited : (139)

References (62)
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    • 39.40 These surface states are energetically unfavorable in the electron transfer reactions considered in this study and are neglected in the calculations
    • 39.40 These surface states are energetically unfavorable in the electron transfer reactions considered in this study and are neglected in the calculations.
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    • note
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    • The self-exchange electron transfer rate constant for the viologen system (S. Dai, thesis. University of Tennessee, 1990) is about one order higher than that of the Fc system [R. M. Neilson, G. E. MacManis, L. K. Safford, and M. J. Weaver, J. Chem. Phys. 93, 2152(1989)]. Since no temperature-dependence measurement was done for the viologen system, the reorganization energy is unknown and thus no conclusion can be drawn by comparing the self-exchange reactions.
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    • note
    • There is some arbitrariness of this definition of the surface density of electrons and the averaged coupling matrix element because the applied potential on different atom layers of the semiconductor are different. But because the coupling between the semiconductor atoms and the redox species decays fast with their distance (with a decay length in the order of 1 Å), and the applied potential varies slowly (with the band bending in the order of 100 nm), it is a good approximation to assume that the density of electrons is the same in the semiconductor surface region of present interest.


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