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表面修饰的α-Fe2O3 光阳极中光生空穴的动力学行为研究及其在太阳能分解水反应中的应用。

Dynamics of photogenerated holes in surface modified α-Fe2O3 photoanodes for solar water splitting.

机构信息

Department of Chemistry, Imperial College London, South Kensington Campus, London, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2012 Sep 25;109(39):15640-5. doi: 10.1073/pnas.1118326109. Epub 2012 Jul 16.

Abstract

This paper addresses the origin of the decrease in the external electrical bias required for water photoelectrolysis with hematite photoanodes, observed following surface treatments of such electrodes. We consider two alternative surface modifications: a cobalt oxo/hydroxo-based (CoO(x)) overlayer, reported previously to function as an efficient water oxidation electrocatalyst, and a Ga(2)O(3) overlayer, reported to passivate hematite surface states. Transient absorption studies of these composite electrodes under applied bias showed that the cathodic shift of the photocurrent onset observed after each of the surface modifications is accompanied by a similar cathodic shift of the appearance of long-lived hematite photoholes, due to a retardation of electron/hole recombination. The origin of the slower electron/hole recombination is assigned primarily to enhanced electron depletion in the Fe(2)O(3) for a given applied bias.

摘要

本文探讨了在对氧化铁光阳极进行表面处理后,观察到水光电解所需的外部电偏压降低的原因。我们考虑了两种替代的表面改性方法:一种是基于钴氧/羟基金属(CoO(x))的覆盖层,之前有报道称其作为一种有效的水氧化电催化剂;另一种是 Ga(2)O(3)覆盖层,据报道可以钝化氧化铁表面态。对这些复合电极在施加偏压下的瞬态吸收研究表明,在每种表面改性之后观察到的光电流起始的阴极位移伴随着长寿命氧化铁光空穴出现的类似阴极位移,这是由于电子/空穴复合的延迟。较慢的电子/空穴复合的原因主要归因于在给定的施加偏压下,Fe(2)O(3)中的电子耗尽增强。

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