Synergistically coupling P-doped Mo2C@N, P dual-doped carbon-nanoribbons as an efficient electrocatalyst for the hydrogen evolution reaction

被引:3
|
作者
Wang, Baoli [1 ,2 ]
Huang, Yuhao [1 ]
Ai, Yijing [1 ]
Yao, Yucen [1 ,3 ]
Shi, Fan [1 ]
Xu, Shiguan [1 ]
Zhang, Zejun [1 ,4 ]
Wang, Xianghui [1 ]
Sun, Wei [1 ]
机构
[1] Hainan Normal Univ, Coll Chem & Chem Engn, Key Lab Funct Mat & Photoelectrochem Haikou, Key Lab Water Pollut Treatment & Resource Rouse H, Haikou 571158, Hainan, Peoples R China
[2] Hainan Technol & Business Coll, Coll Hlth Sci, Haikou 570203, Hainan, Peoples R China
[3] Chongqing Univ Arts & Sci, Coll Chem & Environm Engn, Chongqing 402160, Peoples R China
[4] Zhaotong Univ, Coll Chem & Chem Engn, Zhaotong 657000, Peoples R China
基金
中国国家自然科学基金;
关键词
MOLYBDENUM CARBIDE; HIGHLY EFFICIENT; NANOPARTICLES; NITROGEN; PHOSPHIDE; MATRIX;
D O I
10.1039/d2nj01553f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing non-noble and high-performance electrocatalysts towards the hydrogen evolution reaction (HER) in both acidic and alkaline media remains a stern challenge. Herein, the composite of P-doped Mo2C and a hierarchically ultrathin N, P-doped carbon nanoribbon network (P-Mo2C/NPC) is proposed through a facile simultaneous phosphating-carbonization strategy, in which biomass and phosphomolybdic acid (PMA) were employed as the carbon precursor and metal precursor, respectively. The doping of the electronegative P heteroatom increases the active sites, weakens the Mo-H bond strength in the HER, and facilitates the electron transfer. Consequently, the synthesized catalyst exhibits good intrinsic activity towards the HER, and shows low overpotentials of 172 mV and 118 mV to afford the current density of 10 mA cm(-2) in 0.5 M H2SO4 and 1.0 M KOH electrolyte, respectively. Furthermore, the synthesized catalyst can sustain 24 h with stable performance, which is greatly favorable for industrial applications. This work may shed some light on the rational design and manufacture of HER electrocatalysts with high compatibility to different electrolytic environments.
引用
收藏
页码:11389 / 11397
页数:9
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