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,Wen-Jia Xu,Chunxiao Lv,Lijie Zhang,Mohsen Shakouri,Yanhua Peng,Yan 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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