Sulfur Vacancy-Rich O-Doped 1T-MoS2 Nanosheets for Exceptional Photocatalytic Nitrogen Fixation over CdS

被引:249
作者
Sun, Benteng [1 ]
Liang, Zhangqian [1 ]
Qian, Yeye [1 ]
Xu, Xuesong [1 ]
Han, Ye [1 ]
Tian, Jian [1 ]
机构
[1] Shandong Univ Sci & Technol, Sch Mat Sci & Engn, Qingdao 266590, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalytic nitrogen fixation; 1T-MoS2; sulfur vacancies; O-doped; CdS nanorods; MOS2 ULTRATHIN NANOSHEETS; HYDROGEN EVOLUTION REACTION; GRAPHITIC CARBON NITRIDE; REDUCED GRAPHENE OXIDE; EXPOSED; 001; FACETS; VISIBLE-LIGHT; MOLYBDENUM-DISULFIDE; OXYGEN VACANCIES; H-2; EVOLUTION; WATER;
D O I
10.1021/acsami.9b20767
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Here, we reported that sulfur vacancy-rich O-doped 1T-MoS2 nanosheets (denoted as SV-1T-MoS2) can surpass the activity of Pt as cocatalysts to assist in the photocatalytic nitrogen fixation of CdS nanorods. SV-1T-MoS2 cocatalysts exhibit sulfur vacancies, O-doping, more metallic 1T phase, and high electronic conductivity, thus leading to the exposure of more active edge sites, high Brunauer-Emmett-Teller surface area, enhanced visible light absorption, and improved electron separation and transfer, which are beneficial for photocatalytic nitrogen fixation. Consequently, the optimized 30 wt % SV-1T-MoS2-/CdS composites exhibit an outstanding nitrogen fixation rate of 8220.83 mu mol L-1 h(-1) g(-1) and long-term stability under simulated solar light irradiation, significantly higher than pure CdS nanorods, CdS-Pt (0.1 wt %), and 30 wt % 1T-MoS2/CdS composites. The catalytic mechanism of photocatalytic nitrogen fixation on SV-1T-MoS2 is discussed by density functional theory calculations.
引用
收藏
页码:7257 / 7269
页数:13
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