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高效活性氧化物光电阴极用于光电化学水还原。

Highly active oxide photocathode for photoelectrochemical water reduction.

机构信息

Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne, Laboratory of Photonics and Interfaces, Station 6, CH-1015 Lausanne, Switzerland.

出版信息

Nat Mater. 2011 Jun;10(6):456-61. doi: 10.1038/nmat3017. Epub 2011 May 8.

Abstract

A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H(2) production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents of up to -7.6 mA cm(-2) at a potential of 0 V versus the reversible hydrogen electrode at mild pH. The electrodes remained active after 1 h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%.

摘要

一种清洁高效的方法来克服化石燃料的有限供应和温室效应是通过半导体/水结的光电化学电池将阳光和水转化为氢气燃料,其中能量收集和水电解被结合到单个半导体电极中。我们提出了一种用于太阳能 H(2)生产的高效光阴极,由电沉积的氧化亚铜组成,通过掺杂氧化锌和氧化钛的纳米层保护其免受水的光解分解,并通过电沉积的铂纳米颗粒激活其用于析氢反应。研究了不同表面保护成分的作用,在最佳情况下,电极在温和 pH 值下的 0 V 对可逆氢电极的电位下显示出高达 -7.6 mA cm(-2)的光电流。电极在 1 小时的测试后仍然保持活性,发现氧化亚铜在还原反应过程中是稳定的,法拉第效率估计接近 100%。

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