Enhancing photocatalytic activity in monolayer MoS2 by charge compensated co-doping with P and Cl: First principles study

被引:14
|
作者
Zhao, Yafei [1 ,2 ]
Sun, Yizhe [1 ,2 ]
Hu, Xiaoying [3 ,4 ]
Tu, Jian [1 ,2 ]
Gao, Qinwu [1 ,2 ]
Wang, Wei [1 ,2 ]
Ruan, Xuezhong [1 ,2 ]
Wang, Fengqiu [1 ,2 ]
Liu, Wenqing [1 ,2 ,5 ]
Zou, Wenqin [6 ]
Xu, Yongbing [1 ,2 ]
He, Liang [1 ,2 ]
机构
[1] Nanjing Univ, Sch Elect Sci & Engn, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[3] Changchun Univ, Coll Sci, Changchun 130022, Jilin, Peoples R China
[4] Changchun Univ, Lab Mat Design & Quantum Simulat, Changchun 130022, Jilin, Peoples R China
[5] Royal Holloway Univ London, Dept Elect Engn, Egham TW20 0EX, Surrey, England
[6] Nanjing Univ, Dept Phys, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
来源
MOLECULAR CATALYSIS | 2019年 / 468卷
基金
中国国家自然科学基金;
关键词
P-Cl co-doping; Flat impurity level; Charge compensated; Catalytic active sites; ANATASE TIO2; MECHANISM; GRAPHENE; BANDGAP; G-C3N4;
D O I
10.1016/j.mcat.2019.02.002
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
Recently, P doped ultra-thin MoS2 film has demonstrated enhanced photocatalytic property. However, the flat impurity level within the bulk band gap acting as the recombination center hinders the photocatalytic performance. This impurity level is induced by P, whose outer shell has one electron less than S. Thus, charge compensated doping P and Cl together is adopted here to remove the impurity levels. Using first principles study, we report the doping site, formation energy, electronic and photocatalytic properties of P and Cl co-doped mono layer MoS2. It is found that P and Cl atoms tend to settle at S sites (P-s and Cl-s) instead of Mo sites or interstitial. Interestingly, P-s-Cl-s co-doping can enhance the photocatalytic activity of MoS2 by removing the flat impurity level and increasing the number of catalytic active sites.
引用
收藏
页码:94 / 99
页数:6
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