Activating VS2basal planes for enhanced NRR electrocatalysis: the synergistic role of S-vacancies and B dopants

被引:172
作者
Li, Qingqing [1 ]
Guo, Yali [1 ]
Tian, Ye [2 ]
Liu, Wuming [3 ]
Chu, Ke [1 ]
机构
[1] Lanzhou Jiaotong Univ, Sch Mat Sci & Engn, Lanzhou 730070, Peoples R China
[2] Hebei North Univ, Coll Sci, Dept Phys, Zhangjiakou 075000, Hebei, Peoples R China
[3] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
NITROGEN REDUCTION; N-2; REDUCTION; OXYGEN VACANCIES; GRAPHENE; INTERFACE; AMMONIA; NH3; NANOSHEETS; FIXATION; ELECTROSYNTHESIS;
D O I
10.1039/d0ta05282e
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
The nitrogen reduction reaction (NRR) is a pivotal step in electrochemical N(2)fixation to NH3. VS(2)holds great promise as a NRR electrocatalyst, but its high activity requires the sufficient activation of inert basal planes. Herein, we demonstrate the first successful activation of VS(2)basal planes toward the NRR by introducing S-vacancies (Vs) and B-dopants. The theoretical calculations unravel that the synergistic role of V(S)and B-dopants enables the most effective activation of VS(2)basal planes by creating unique B-adjacent-unsaturated-V active sites that can significantly promote the NRR while suppressing hydrogen evolution. The synthesized B-doped VS(2)nanoflowers with enriched surface Vs delivered an NH(3)yield of 55.7 mu g h(-1)mg(-1)(-0.4 V) and a faradaic efficiency (FE) of 16.4% (-0.2 V) and represent the best V-based catalysts to date. Our theoretical and experimental findings may facilitate the exploration and understanding of advanced transition-metal disulfide catalysts for the NRR.
引用
收藏
页码:16195 / 16202
页数:8
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