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Photoelectrochemical and Impedance Spectroscopic Investigation of Water Oxidation with “Co–Pi”-Coated Hematite Electrodes

机译:“Co - pi” - 赤铁矿电极水氧化的光电化学和阻抗光谱研究

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摘要

Uniform thin films of hematite (α-Fe2O3) 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.
机译:通过稳态和瞬态光电化学测量以及阻抗谱研究了通过原子层沉积(ALD)沉积的赤铁矿均匀薄膜(α-Fe2O3),该原子层涂覆了不同量的磷酸钴催化剂“ Co-Pi”。为了阐明Co-Pi增强赤铁矿电极的水分解性能的机理,进行了作为Co-Pi厚度函数的系统研究。发现在光照下,Co-Pi催化剂可以有效地收集和存储来自赤铁矿电极的光生空穴。这种电荷分离减少了表面状态的重组,从而导致水氧化效率提高。还发现,较厚的Co-Pi膜可提高水氧化效率,这归因于优异的电荷分离能力和多孔催化膜表面积的增加。这些综合的结果为Co-Pi催化剂与用于水分解应用的半导体电极结合的增强和局限性提供了重要的新认识。

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