Sponge Assembled by Graphene Nanocages with Double Active Sites to Accelerate Alkaline HER Kinetics

被引:57
作者
Gu, Yu [1 ]
Xi, Baojuan [1 ]
Wei, Ruchao [1 ]
Fu, Qiang [1 ]
Qain, Yitai [1 ,2 ,3 ]
Xiong, Shenglin [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, State Key Lab Crystal Mat,Minist Educ, Jinan 250100, Peoples R China
[2] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni single atoms; Ni nanoparticles; graphene nanocages; double active sites; alkaline hydrogen evolution reaction; HYDROGEN-EVOLUTION REACTION; POROUS CARBON; HIGHLY EFFICIENT; SINGLE-ATOM; ELECTROCATALYSTS; NANOPARTICLES; NANOSHEETS; CURVATURE; SURFACE; MOS2;
D O I
10.1021/acs.nanolett.0c03565
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Elaborate design of novel hybrid structures for hydrogen-evolution electrocatalysts is a crucial strategy for synergistically accelerating the reaction kinetics of water splitting. Herein, we prepare a three-dimensional (3D) sponge assembled by graphene nanocages (SGNCs) in which Ni nanoparticles and Ni single atoms coexist via a facile one-pot selft-emplating and self-catalytic strategy. Driven by simultaneous atomization and agglomeration under higher temperature, dual active sites of single atoms and nanoparticles are formed on graphene nanocages. Benefiting from the unique 3D porous structure and dual active sites, the SGNCs exhibit excellent hydrogen evolution reaction (HER) performance, which affords the current density of 10 mA cm(-2). at a low overpotential of 27 mV. Theoretical calculations reveal that the interaction between single atoms and nanoparticles promotes HER kinetics. The controlled engineering strategy of non-noble metal-based hybrid materials provides prospects for innovative electrocatalyst development.
引用
收藏
页码:8375 / 8383
页数:9
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