材料科学
钙钛矿(结构)
析氧
电解质
介孔材料
石墨
卤化物
分解水
催化作用
水溶液
化学工程
电极
电化学
光催化
纳米技术
无机化学
化学
复合材料
有机化学
物理化学
工程类
作者
Isabella Poli,Ulrich Hintermair,Miriam Regue,Santosh Kumar,Emma V. Sackville,Jenny Baker,Trystan Watson,Salvador Eslava,Petra J. Cameron
标识
DOI:10.1038/s41467-019-10124-0
摘要
Metal-halide perovskites have been widely investigated in the photovoltaic sector due to their promising optoelectronic properties and inexpensive fabrication techniques based on solution processing. Here we report the development of inorganic CsPbBr3-based photoanodes for direct photoelectrochemical oxygen evolution from aqueous electrolytes. We use a commercial thermal graphite sheet and a mesoporous carbon scaffold to encapsulate CsPbBr3 as an inexpensive and efficient protection strategy. We achieve a record stability of 30 h in aqueous electrolyte under constant simulated solar illumination, with currents above 2 mA cm-2 at 1.23 VRHE. We further demonstrate the versatility of our approach by grafting a molecular Ir-based water oxidation catalyst on the electrolyte-facing surface of the sealing graphite sheet, which cathodically shifts the onset potential of the composite photoanode due to accelerated charge transfer. These results suggest an efficient route to develop stable halide perovskite based electrodes for photoelectrochemical solar fuel generation.
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