Activating the MoS2 Basal Plane toward Enhanced Solar Hydrogen Generation via in Situ Photoelectrochemical Control

被引:32
|
作者
Xun, Wei [1 ,2 ]
Wang, Yongjie [3 ]
Fan, Ronglei [1 ,2 ]
Mu, Qiaoqiao [4 ]
Ju, Sheng [1 ,2 ,5 ]
Peng, Yang [4 ]
Shen, Mingrong [1 ,2 ]
机构
[1] Soochow Univ, Jiangsu Key Lab Thin Films, Sch Phys Sci & Technol, Suzhou 215006, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215006, Peoples R China
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[4] Soochow Univ, Coll Energy, Soochow Inst Energy & Mat Innovat, Prov Key Lab Adv Carbon Mat & Wearable Energy Tec, Suzhou 215006, Peoples R China
[5] Univ Calif Berkeley, Dept Phys, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
LAYERED DOUBLE HYDROXIDE; SILICON PHOTOCATHODES; CATALYTIC-ACTIVITY; SULFUR VACANCIES; EFFICIENT; EVOLUTION; SURFACE; TIO2; HETEROSTRUCTURES; NANOSHEETS;
D O I
10.1021/acsenergylett.0c02320
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
Developing robust, low-cost, and scalable catalysts for photo-electrochemical (PEC) water splitting devices is crucial for the sustainable hydrogen evolution reaction (HER). MoS2 has emerged as a potent alternative to Pt-based catalysts for the HER. However, the active sites of 2H-MoS2 are reported to locate at the edges, leaving a large number of inert basal planes useless. Herein, a facile strategy is reported to activate the MoS2 basal plane via an in situ PEC protocol. Both experimental studies and theoretical calculations reveal the emergence of O-Mo-S sites on the MoS2 basal planes, which enable not only enhancing its intrinsic conductivity but also modulating the adsorption behavior of H atoms and consequent HER activity. As a result, the MoS2-decorated Si photocathodes exhibit an applied bias photon-to-current efficiency of 4.9% under the simulated AM1.5G illumination. This study offers a potential scalable route for the fabrication of high-performance and precious metal-free solar-to-fuel devices.
引用
收藏
页码:267 / 276
页数:10
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