非阻塞I/O
钌
异质结
分解水
材料科学
纳米片
催化作用
制氢
化学工程
密度泛函理论
电化学
无机化学
化学
纳米技术
物理化学
光电子学
电极
计算化学
工程类
光催化
生物化学
作者
Rui Liu,Mingzi Sun,Xiangjian Liu,Zunhang Lv,Xinyu Yu,Jinming Wang,Yarong Liu,Liuhua Li,Xiao Feng,Wenxiu Yang,Bolong Huang,Bo Wang
标识
DOI:10.1002/anie.202312644
摘要
Developing highly efficient and stable hydrogen production catalysts for electrochemical water splitting (EWS) at industrial current densities remains a great challenge. Herein, we proposed a heterostructure-induced-strategy to optimize the metal-support interaction (MSI) and the EWS activity of Ru-Ni3 N/NiO. Density functional theory (DFT) calculations firstly predicted that the Ni3 N/NiO-heterostructures can improve the structural stability, electronic distributions, and orbital coupling of Ru-Ni3 N/NiO compared to Ru-Ni3 N and Ru-NiO, which accordingly decreases energy barriers and increases the electroactivity for EWS. As a proof-of-concept, the Ru-Ni3 N/NiO catalyst with a 2D Ni3 N/NiO-heterostructures nanosheet array, uniformly dispersed Ru nanoparticles, and strong MSI, was successfully constructed in the experiment, which exhibited excellent HER and OER activity with overpotentials of 190 mV and 385 mV at 1000 mA cm-2 , respectively. Furthermore, the Ru-Ni3 N/NiO-based EWS device can realize an industrial current density (1000 mA cm-2 ) at 1.74 V and 1.80 V under alkaline pure water and seawater conditions, respectively. Additionally, it also achieves a high durability of 1000 h (@ 500 mA cm-2 ) in alkaline pure water.
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