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光电化学和阻抗光谱研究“Co-Pi”涂层赤铁矿电极的水氧化。

Photoelectrochemical and impedance spectroscopic investigation of water oxidation with "Co-Pi"-coated hematite electrodes.

机构信息

Department of Chemistry, Michigan State University, East Lansing, Michigan 48824-1322, USA.

出版信息

J Am Chem Soc. 2012 Oct 10;134(40):16693-700. doi: 10.1021/ja306427f. Epub 2012 Sep 27.

Abstract

Uniform thin films of hematite (α-Fe(2)O(3)) deposited by atomic layer deposition (ALD) coated with varying amounts of the cobalt phosphate catalyst, "Co-Pi," were investigated with steady-state and transient photoelectrochemical measurements and impedance spectroscopy. Systematic studies as a function of Co-Pi thickness were performed in order to clarify the mechanism by which Co-Pi enhances the water-splitting performance of hematite electrodes. It was found that under illumination, the Co-Pi catalyst can efficiently collect and store photogenerated holes from the hematite electrode. This charge separation reduces surface state recombination which results in increased water oxidation efficiency. It was also found that thicker Co-Pi films produced increased water oxidation efficiencies which is attributed to a combination of superior charge separation and increased surface area of the porous catalytic film. These combined results provide important new understanding of the enhancement and limitations of the Co-Pi catalyst coupled with semiconductor electrodes for water-splitting applications.

摘要

通过原子层沉积(ALD)沉积的具有均匀厚度的赤铁矿(α-Fe(2)O(3))薄膜,其表面涂覆有不同量的磷酸钴催化剂 "Co-Pi",采用稳态和瞬态光电化学测量和阻抗谱进行了研究。为了阐明 Co-Pi 增强赤铁矿电极水分解性能的机制,进行了 Co-Pi 厚度的系统研究。结果发现,在光照下,Co-Pi 催化剂可以有效地从赤铁矿电极收集和储存光生空穴。这种电荷分离减少了表面态复合,从而提高了水氧化效率。还发现,较厚的 Co-Pi 薄膜产生了更高的水氧化效率,这归因于优异的电荷分离和多孔催化膜表面积的增加的综合作用。这些综合结果为 Co-Pi 催化剂与半导体电极在水分解应用中的增强和限制提供了重要的新认识。

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