过电位
铑
材料科学
纳米晶
电解水
电解
多孔性
高分辨率透射电子显微镜
制氢
氢
纳米技术
分解水
化学工程
催化作用
塔菲尔方程
化学物理
透射电子显微镜
化学
物理化学
电化学
电极
复合材料
有机化学
光催化
工程类
电解质
作者
Yang Gao,Yurui Xue,Qi Lu,Chengyu Xing,Xuchen Zheng,Feng He,Yuliang Li
标识
DOI:10.1038/s41467-022-32937-2
摘要
The realization of the efficient hydrogen conversion with large current densities at low overpotentials represents the development trend of this field. Here we report the atomic active sites tailoring through a facile synthetic method to yield well-defined Rhodium nanocrystals in aqueous solution using formic acid as the reducing agent and graphdiyne as the stabilizing support. High-resolution high-angle annular dark-field scanning-transmission electron microscopy images show the high-density atomic steps on the faces of hexahedral Rh nanocrystals. Experimental results reveal the formation of stable sp-C~Rh bonds can stabilize Rh nanocrystals and further improve charge transfer ability in the system. Experimental and density functional theory calculation results solidly demonstrate the exposed high active stepped surfaces and various metal atomic sites affect the electronic structure of the catalyst to reduce the overpotential resulting in the large-current hydrogen production from saline water. This exciting result demonstrates unmatched electrocatalytic performance and highly stable saline water electrolysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI