Gu Yu, Xi Baojuan, Wei Ruchao, Fu Qiang, Qain Yitai, Xiong Shenglin
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, P.R. China.
School of Chemistry and Materials Science and Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei 230026, P.R. China.
Nano Lett. 2020 Nov 11;20(11):8375-8383. doi: 10.1021/acs.nanolett.0c03565. Epub 2020 Oct 19.
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 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.
精心设计用于析氢电催化剂的新型混合结构是协同加速水分解反应动力学的关键策略。在此,我们制备了一种由石墨烯纳米笼组装而成的三维(3D)海绵(SGNCs),其中镍纳米颗粒和镍单原子通过简便的一锅自模板和自催化策略共存。在较高温度下同时发生雾化和团聚的驱动下,石墨烯纳米笼上形成了单原子和纳米颗粒的双活性位点。受益于独特的3D多孔结构和双活性位点,SGNCs表现出优异的析氢反应(HER)性能,在27 mV的低过电位下可提供10 mA cm的电流密度。理论计算表明,单原子与纳米颗粒之间的相互作用促进了HER动力学。基于非贵金属的混合材料的可控工程策略为创新电催化剂的开发提供了前景。