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BiVO(4)/CuWO(4) 异质结光阳极用于高效太阳能驱动水氧化。

BiVO(4)/CuWO(4) heterojunction photoanodes for efficient solar driven water oxidation.

机构信息

Department of Chemical and Biological Engineering, Colorado School Mines, Golden, CO 80401, USA.

出版信息

Phys Chem Chem Phys. 2013 Mar 7;15(9):3273-8. doi: 10.1039/c2cp44577h. Epub 2013 Jan 25.

Abstract

BiVO(4)/CuWO(4) heterojunction electrodes were prepared using spray deposition of a highly porous bismuth vanadate film onto the surface of an electrodeposited three dimensional network connected copper tungstate. Bilayer BiVO(4)/CuWO(4)/fluorine doped tin oxide glass (FTO) electrodes demonstrated higher photocurrent magnitudes than either with BiVO(4)/FTO or CuWO(4)/FTO electrodes in 1.0 M Na(2)SO(4) electrolyte buffered at pH 7. The photocurrent is enhanced by the formation of the heterojunction that aids charge carrier collection brought about by the band edge offsets. When the pH 7 buffered electrolytes contained 1.0 M bicarbonate is employed instead of 1.0 M sulfate, the charge transfer resistance was decreased. This led to nearly 1.8 times the photocurrent density at 1.0 V vs. Ag/AgCl. The photocurrent was stable over 24 hours in bicarbonate electrolyte.

摘要

BiVO(4)/CuWO(4) 异质结电极是通过将高度多孔的钒酸铋薄膜喷涂在电沉积的三维相互连接的铜钨酸盐表面上制备的。在 pH 值为 7 的 1.0 M Na(2)SO(4)电解质缓冲液中,双层 BiVO(4)/CuWO(4)/掺氟氧化锡玻璃 (FTO) 电极的光电流强度高于 BiVO(4)/FTO 或 CuWO(4)/FTO 电极。异质结的形成促进了载流子的收集,从而增强了光电流,这是由于能带边缘的偏移。当 pH 值为 7 的缓冲电解质中使用 1.0 M 碳酸氢盐而不是 1.0 M 硫酸盐时,电荷转移电阻降低。这导致在 1.0 V 对 Ag/AgCl 时的光电流密度增加近 1.8 倍。在碳酸氢盐电解质中,光电流在 24 小时内稳定。

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