Vanadium defect-engineering in molybdenum disulfide for electrochemical nitrate reduction

被引:22
作者
Yu, Miao [1 ]
Huang, Hao [2 ]
Hu, Jie [1 ]
Wang, Shuang [1 ,3 ]
Li, Jinping [3 ]
Wang, Dingsheng [4 ]
机构
[1] Taiyuan Univ Technol, Coll Environm Sci & Engn, Jinzhong 030600, Shanxi, Peoples R China
[2] Univ South Eastern Norway, Dept Microsyst, N-3184 Borre, Norway
[3] Taiyuan Univ Technol, Shanxi Key Lab Gas Energy Efficient & Clean Utili, Taiyuan 030024, Shanxi, Peoples R China
[4] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCATALYTIC REDUCTION; MOS2; WATER; NITROGEN; REMOVAL; VS2;
D O I
10.1039/d2ta06346h
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 electrochemical nitrate reduction reaction (NITRR) provides a promising option for nitrate pollutant removal and ammonia production under ambient conditions, which requires electrocatalysts with high activity. Here, bio-inspired metalloenzymes MoS2 nanoflowers with defect-engineering via vanadium doping (V-MoS2) prepared by a one-step hydrothermal method are verified to show remarkable NITRR capability. The introduction of highly conductive vanadium changes the electron orbitals and the metalloenzyme-like structure of the MoS2, making the 15% V-MoS2 catalyst exhibit a high-efficiency nitrate removal rate of 95% and excellent ammonia selectivity of 89.5% at -1.1 V versus the reversible hydrogen electrode (RHE) in 0.5 M Na2SO4 solution. Density functional theory (DFT) calculations reveal that the reduced energy barrier of 0.41 eV, correlated with hydrogenation of *NO to *NOH, plays a crucial part in the enhanced nitrate removal rate and NH4+ selectivity of V-MoS2. This work opens up a new avenue for the design of bio-inspired metalloenzyme catalysts for the NITRR.
引用
收藏
页码:23990 / 23997
页数:9
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