纳米笼
过电位
电催化剂
石墨烯
材料科学
纳米技术
催化作用
纳米颗粒
贵金属
分解水
化学工程
化学
光催化
物理化学
电化学
有机化学
工程类
电极
作者
Yu Gu,Baojuan Xi,Ruchao Wei,Qiang Fu,Yitai Qain
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-10-19
卷期号:20 (11): 8375-8383
被引量:37
标识
DOI:10.1021/acs.nanolett.0c03565
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 self-templating 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.
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