Highly porous non-precious bimetallic electrocatalysts for efficient hydrogen evolution

被引:504
作者
Lu, Qi [1 ,2 ]
Hutchings, Gregory S. [1 ]
Yu, Weiting [2 ]
Zhou, Yang [3 ]
Forest, Robert V. [1 ]
Tao, Runzhe [4 ]
Rosen, Jonathan [1 ]
Yonemoto, Bryan T. [1 ]
Cao, Zeyuan [5 ]
Zheng, Haimei [4 ]
Xiao, John Q. [3 ]
Jiao, Feng [1 ]
Chen, Jingguang G. [2 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, Ctr Catalyt Sci & Technol, Newark, DE 19716 USA
[2] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[3] Univ Delaware, Dept Phys & Astron, Newark, DE 19716 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[5] Univ Delaware, Dept Mech Engn, Newark, DE 19716 USA
基金
美国国家科学基金会; 美国国家航空航天局;
关键词
ACTIVE EDGE SITES; NANOPARTICLE ELECTROCATALYSTS; MOLYBDENUM CARBIDE; OXYGEN REDUCTION; CATALYTIC-ACTIVITY; ALKALINE; MOS2; OXIDATION; ENERGY; STABILITY;
D O I
10.1038/ncomms7567
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
A robust and efficient non-precious metal catalyst for hydrogen evolution reaction is one of the key components for carbon dioxide-free hydrogen production. Here we report that a hierarchical nanoporous copper-titanium bimetallic electrocatalyst is able to produce hydrogen from water under a mild overpotential at more than twice the rate of state-of-the-art carbon-supported platinum catalyst. Although both copper and titanium are known to be poor hydrogen evolution catalysts, the combination of these two elements creates unique copper-copper-titanium hollow sites, which have a hydrogen-binding energy very similar to that of platinum, resulting in an exceptional hydrogen evolution activity. In addition, the hierarchical porosity of the nanoporous copper-titanium catalyst also contributes to its high hydrogen evolution activity, because it provides a large-surface area for electrocatalytic hydrogen evolution, and improves the mass transport properties. Moreover, the catalyst is self-supported, eliminating the overpotential associated with the catalyst/support interface.
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页数:8
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