A tailored double perovskite nanofiber catalyst enables ultrafast oxygen evolution

被引:380
作者
Zhao, Bote [1 ]
Zhang, Lei [1 ]
Zhen, Dongxing [1 ]
Yoo, Seonyoung [1 ]
Ding, Yong [1 ]
Chen, Dongchang [1 ]
Chen, Yu [1 ]
Zhang, Qiaobao [1 ]
Doyle, Brian [1 ]
Xiong, Xunhui [1 ,2 ]
Liu, Meilin [1 ]
机构
[1] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[2] South China Univ Technol, New Energy Res Inst, Sch Environm & Energy, Guangzhou 510006, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
EFFICIENT WATER OXIDATION; OXIDE FUEL-CELLS; HIGHLY-EFFICIENT; TRANSITION-METALS; ALKALINE-SOLUTION; ION DIFFUSION; SPIN-STATE; SURFACE; REDUCTION; ELECTROCATALYST;
D O I
10.1038/ncomms14586
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
Rechargeable metal-air batteries and water splitting are highly competitive options for a sustainable energy future, but their commercialization is hindered by the absence of cost-effective, highly efficient and stable catalysts for the oxygen evolution reaction. Here we report the rational design and synthesis of a double perovskite PrBa0.5Sr0.5Co1.5Fe0.5O5+delta nanofiber as a highly efficient and robust catalyst for the oxygen evolution reaction. Co-doping of strontium and iron into PrBaCo2O5+delta is found to be very effective in enhancing intrinsic activity (normalized by the geometrical surface area, similar to 4.7 times), as validated by electrochemical measurements and first-principles calculations. Further, the nanofiber morphology enhances its mass activity remarkably (by similar to 20 times) as the diameter is reduced to similar to 20 nm, attributed to the increased surface area and an unexpected intrinsic activity enhancement due possibly to a favourable eg electron filling associated with partial surface reduction, as unravelled from chemical titration and electron energy-loss spectroscopy.
引用
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页数:9
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