Co/MoN hetero-interface nanoflake array with enhanced water dissociation capability achieves the Pt-like hydrogen evolution catalytic performance

被引:160
作者
Sun, Junwei [1 ]
Xu, Wenjia [2 ]
Lv, Chunxiao [2 ]
Zhang, Lijie [2 ]
Shakouri, Mohsen [3 ]
Peng, Yanhua [1 ]
Wang, Qianqian [1 ]
Yang, Xianfeng [4 ]
Yuan, Ding [1 ]
Huang, Minghua [5 ]
Hu, Yongfeng [3 ]
Yang, Dongjiang [2 ]
Zhang, Lixue [1 ]
机构
[1] Qingdao Univ, Coll Chem & Chem Engn, Qingdao 266071, Peoples R China
[2] Qingdao Univ, Sch Environm Sci & Engn, Collaborat Innovat Ctr Marine Biobased Fibers & E, State Key Lab Biofibers & Ecotext, Qingdao 266071, Peoples R China
[3] Canadian Light Source, Saskatoon, SK S7N 0X4, Canada
[4] South China Univ Technol, Analyt & Testing Ctr, Guangzhou 510640, Peoples R China
[5] Ocean Univ China, Sch Mat Sci & Engn, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金; 加拿大自然科学与工程研究理事会;
关键词
MoN; Hetero-interface; Water dissociation; Electrocatalyst; Hydrogen evolution;
D O I
10.1016/j.apcatb.2021.119882
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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/cm(2), 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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页数:8
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