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水热转化 WO 薄膜合成的 α-SnWO 光阴极的光电化学性质及行为。

Photoelectrochemical Properties and Behavior of α-SnWO Photoanodes Synthesized by Hydrothermal Conversion of WO Films.

机构信息

Department of Chemistry and Biochemistry, Worcester Polytechnic Institute , Worcester, Massachusetts 01609, United States.

Department of Chemical Engineering, Worcester Polytechnic Institute , Worcester, Massachusetts 01609, United States.

出版信息

ACS Appl Mater Interfaces. 2017 Jan 18;9(2):1459-1470. doi: 10.1021/acsami.6b12640. Epub 2017 Jan 5.

Abstract

Metal oxides with moderate band gaps are desired for efficient production of hydrogen from sunlight and water via photoelectrochemical (PEC) water splitting. Here, we report an α-SnWO photoanode synthesized by hydrothermal conversion of WO films that achieves photon to current conversion at wavelengths up to 700 nm (1.78 eV). This photoanode is promising for overall PEC water-splitting because the flat-band potential and voltage of photocurrent onset are more negative than the potential of hydrogen evolution. Furthermore, the photoanode utilizes a large portion of the solar spectrum. However, the photocurrent density reaches only a small fraction of that which is theoretically possible. Density functional theory based thermodynamic and electronic structure calculations were performed to elucidate the nature and impact of defects in α-SnWO prepared by this synthetic route, from which hole localization at Sn-at-W antisite defects was determined to be a likely cause for the poor photocurrent. Measurements further showed that the photocurrent decreases over time due to surface oxidation, which was suppressed by improving the kinetics of hole transfer at the semiconductor/electrolyte interface. Alternative synthetic methods and the addition of protective coatings and/or oxygen evolution catalysts are suggested to improve the PEC performance and stability of this promising α-SnWO material.

摘要

具有适中带隙的金属氧化物是通过光电化学(PEC)水分解利用太阳光和水高效生产氢气所需要的。在这里,我们报告了一种通过 WO 薄膜水热转化合成的α-SnWO 光阳极,其在波长高达 700nm(1.78eV)处实现了光子到电流的转换。由于平带电位和光电流起始电压比析氢电位更负,因此该光阳极有望用于整体 PEC 水分解。此外,该光阳极利用了很大一部分太阳光谱。然而,光电流密度仅达到理论上可能值的一小部分。通过基于密度泛函理论的热力学和电子结构计算,阐明了通过这种合成路线制备的α-SnWO 中缺陷的性质和影响,结果表明,在 Sn 位 W 反位缺陷处的空穴局域化是导致光电流较差的可能原因。进一步的测量表明,由于表面氧化,光电流随时间下降,通过改善半导体/电解质界面处空穴转移的动力学可以抑制这种情况。建议采用替代的合成方法和添加保护层和/或析氧催化剂来提高这种有前途的α-SnWO 材料的 PEC 性能和稳定性。

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