Iridium-based double perovskites for efficient water oxidation in acid media

被引:412
作者
Diaz-Morales, Oscar [1 ]
Raaijman, Stefan [1 ]
Kortlever, Ruud [1 ]
Kooyman, Patricia J. [2 ,3 ]
Wezendonk, Tim [2 ]
Gascon, Jorge [2 ]
Fu, W. T. [1 ]
Koper, Marc T. M. [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, POB 9502, NL-2300 RA Leiden, Netherlands
[2] Delft Univ Technol, Fac Sci Appl, ChemE, Julianalaan 136, NL-2628 BL Delft, Netherlands
[3] Univ Cape Town, Dept Chem Engn, Private Bag X3, ZA-7701 Rondebosch, South Africa
关键词
OXYGEN EVOLUTION REACTION; HYDROGEN-PRODUCTION; CRYSTAL-STRUCTURES; OXIDE SURFACES; SPACE GROUP; STABILITY; ELECTROCHEMISTRY; ELECTROCATALYSTS; ELECTROLYSIS; METALS;
D O I
10.1038/ncomms12363
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
The development of active, cost-effective and stable oxygen-evolving catalysts is one of the major challenges for solar-to-fuel conversion towards sustainable energy generation. Iridium oxide exhibits the best available compromise between catalytic activity and stability in acid media, but it is prohibitively expensive for large-scale applications. Therefore, preparing oxygen-evolving catalysts with lower amounts of the scarce but active and stable iridium is an attractive avenue to overcome this economical constraint. Here we report on a class of oxygen-evolving catalysts based on iridium double perovskites which contain 32 wt% less iridium than IrO2 and yet exhibit a more than threefold higher activity in acid media. According to recently suggested benchmarking criteria, the iridium double perovskites are the most active catalysts for oxygen evolution in acid media reported until now, to the best of our knowledge, and exhibit similar stability to IrO2.
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页数:6
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