Vapor-assisted engineering heterostructure of 1D Mo3N2 nanorod decorated with nitrogen-doped carbon for rapid pH-Universal hydrogen evolution reaction

被引:9
作者
Wu, Qikai [1 ]
Zhao, Dengke [1 ]
Yu, Xiaolong [2 ]
Xu, Jinchang [3 ]
Wang, Nan [3 ]
Zhou, Wei [1 ]
Li, Ligui [1 ]
机构
[1] South China Univ Technol, Sch Environm & Energy, New Energy Res Inst, Guangzhou Key Lab Surface Chem Energy Mat, Guangzhou 510006, Peoples R China
[2] Guangdong Univ Petrochem Technol, Sch Environm Sci & Engn, Guangdong Prov Key Lab Petrochem Pollut Proc & Co, Maoming 525000, Guangdong, Peoples R China
[3] Jinan Univ, Guangdong Prov Engn Technol Res Ctr Vacuum Coatin, Dept Phys,Siyuan Lab, Guangdong Prov Key Lab Opt Fiber Sensing & Commun, Guangzhou 510632, Guangdong, Peoples R China
基金
中国博士后科学基金;
关键词
Heterostructure; Molybdenum nitride nanorod; Nitrogen-doped carbon; Hydrogen evolution reaction; METAL-ORGANIC FRAMEWORKS; EFFICIENT HYDROGEN; NANOSHEETS; NITRIDE; ELECTROCATALYSTS; PERFORMANCE; COMPOSITES; PHOSPHIDE; G-C3N4; ANODE;
D O I
10.1016/j.ijhydene.2021.11.184
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
Reasonable construction of heterostructure is of significance yet a great challenge towards efficient pH-universal catalysts for hydrogen evolution reaction (HER). Herein, a facial strategy coupling gas-phase nitridation with simultaneous heterogenization has been developed to synthesize heterostructure of one-dimensional (1D) Mo3N2 nanorod decorated with ultrathin nitrogen-doped carbon layer (Mo3N2@NC NR). Thereinto, the collaborative interface of Mo3N2 and NC is conducive to accomplish rapid electron transfer for reaction kinetics and weaken the Mo-H-ads bond for boosting the intrinsic activity of catalysts. As expected, Mo3N2@NC NR delivers an excellent catalytic activity for HER with low overpotentials of 85, 129, and 162 mV to achieve a current density of 10 mA cm(-2) in alkaline, acidic, and neutral electrolytes, respectively, and favorable long-term stability over a broad pH range. As for practical application in electrocatalytic water splitting (EWS) under alkaline, Mo3N2@NC NR parallel to NiFe-LDH-based EWS also exhibits a low cell voltage of 1.55 V and favorable durability at a current density of 10 mA cm(-2) , even surpassing the Pt/C parallel to RuO2 -based EWS (1.60 V). Consequently, the proposed suitable methodology here may accelerate the development of Mo-based electrocatalysts in pH-universal non-noble metal materials for energy conversion. (C) 2021 Published by Elsevier Ltd on behalf of Hydrogen Energy Publications LLC.
引用
收藏
页码:5064 / 5073
页数:10
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