Hierarchical CoS2/MoS2 flower-like heterostructured arrays derived from polyoxometalates for efficient electrocatalytic nitrogen reduction under ambient conditions

被引:54
作者
Wang, Chenglong [1 ]
Yang, Mengle [1 ]
Wang, Xinming [1 ]
Ma, Huiyuan [1 ]
Tian, Yu [2 ]
Pang, Haijun [1 ]
Tan, Lichao [1 ]
Gao, Keqing [3 ]
机构
[1] Harbin Univ Sci & Technol, Sch Mat Sci & Chem Engn, Harbin 150040, Peoples R China
[2] Jilin Engn Normal Univ, Inst Interdisciplinary Quantum Informat Technol, Changchun 130052, Jilin, Peoples R China
[3] Beijing Bluestar Tech Ctr, Beijing Caron Fiber Engn Technol Res Ctr, Beijing 101318, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Polyoxometalates; Molybdenum disulfide; Cobalt disulfide; Electrocatalyst; Nitrogen reduction reaction; N-2; REDUCTION; ELECTROCHEMICAL SYNTHESIS; EVOLUTION REACTION; AMMONIA-SYNTHESIS; COBALT SULFIDE; DOPED CARBON; PERFORMANCE; GRAPHENE; MOS2; NANOSHEETS;
D O I
10.1016/j.jcis.2021.11.087
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
Electrochemical nitrogen reduction reaction (NRR) has been identified as a prospective alternative for sustainable ammonia production. Developing cost-effective and highly efficient electrocatalysts is critical for NRR under ambient conditions. Herein, the hierarchical cobalt-molybdenum bimetallic sulfide (CoS2/MoS2) flower-like heterostructure assembled from well-aligned nanosheets has been easily fabricated through a one-step strategy. The efficient synergy between different components and the formation of heterostructure in CoS2/MoS2 nanosheets with abundant active sites makes the non-noble metal catalyst CoS2/MoS2 highly effective in NRR, with a high NH3 yield rate (38.61 mu g h(-1) mg(cat).(-1)), Faradaic efficiency (34.66%), high selectivity (no formation of hydrazine) and excellent long-term stability in 1.0 mol L-1 K2SO4 electrolyte (pH = 3.5) at -0.25 V versus the reversible hydrogen electrode (vs. RHE) under ambient conditions, exceeding much recently reported cobalt- and molybdenum-based materials, even catch up with some noble-metal-based catalyst. Density functional theory (DFT) calculation indicates that the formation of N2H* species on CoS2(200)/MoS2(002) is the rate-determining step via both the alternating and distal pathways with the maximum DG values (1.35 eV). These results open up opportunities for the development of efficient non-precious bimetal-based catalysts for NRR. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:815 / 824
页数:10
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