Metal-encapsulated organolead halide perovskite photocathode for solar-driven hydrogen evolution in water

被引:178
作者
Crespo-Quesada, Micaela [1 ]
Pazos-Outon, Luis M. [2 ]
Warnan, Julien [1 ]
Kuehnel, Moritz F. [1 ]
Friend, Richard H. [2 ]
Reisner, Erwin [1 ]
机构
[1] Univ Cambridge, Dept Chem, Christian Doppler Lab Sustainable SynGas Chem, Cambridge CB2 1EW, England
[2] Univ Cambridge, Dept Phys, Cambridge CB3 OHE, England
基金
英国工程与自然科学研究理事会;
关键词
DIFFUSION LENGTHS; LEAD ACETATE; CELLS; PERFORMANCE; EFFICIENT; TEMPERATURE; STABILITY; LAYER; CRYSTALLIZATION; PHOTOANODES;
D O I
10.1038/ncomms12555
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lead-halide perovskites have triggered the latest breakthrough in photovoltaic technology. Despite the great promise shown by these materials, their instability towards water even in the presence of low amounts of moisture makes them, a priori, unsuitable for their direct use as light harvesters in aqueous solution for the production of hydrogen through water splitting. Here, we present a simple method that enables their use in photoelectrocatalytic hydrogen evolution while immersed in an aqueous solution. Field's metal, a fusible InBiSn alloy, is used to efficiently protect the perovskite from water while simultaneously allowing the photogenerated electrons to reach a Pt hydrogen evolution catalyst. A record photocurrent density of -9.8mAcm(-2) at 0 V versus RHE with an onset potential as positive as 0.95 +/- 0.03 V versus RHE is obtained. The photoelectrodes show remarkable stability retaining more than 80% of their initial photocurrent for similar to 1 h under continuous illumination.
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页数:7
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