过电位
离解(化学)
电催化剂
催化作用
材料科学
密度泛函理论
化学工程
电子转移
水的自电离
氮化物
氢
分解水
吸附
纳米技术
化学物理
化学
光化学
电极
电化学
物理化学
计算化学
有机化学
工程类
光催化
生物化学
图层(电子)
作者
Junwei Sun,Wenjia Xu,Chunxiao Lv,Lijie Zhang,Mohsen Shakouri,Yanhua Peng,Qianqian Wang,Xianfeng Yang,Ding Yuan,Minghua Huang,Yongfeng Hu,Dongjiang Yang,Lixue Zhang
标识
DOI:10.1016/j.apcatb.2021.119882
摘要
Developing high-performance electrocatalyst for hydrogen evolution reaction (HER) is paramount for hydrogen economy. Molybdenum-based nitrides (MoNx) are promising HER catalysts in alkaline condition; however, the performance is greatly limited by the weak water dissociation capacity to form adsorbed H* from H2O, which is crucial but long ignored. Herein, we develop a new strategy to enhance the water dissociation capacity of MoN by forming Co/MoN hetero-interface nanoflake array. The electronic structure of MoN can be effectively modulated by the electron transfer occurred at the Co/MoN hetero-interface. Co/MoN nanoarray also possesses a significantly increased electrochemically active surface area. Co/MoN nanoarray thus exhibits remarkable HER activity with an overpotential of 132 mV to reach 100 mA/cm2, which is among the best non-noble metal HER electrocatalysts in alkaline solution. The very low energy barrier of -0.04 eV for water dissociation on Co/MoN calculated by density functional theory confirms the strong water dissociation capability.
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