Electrochemical generation of sulfur vacancies in the basal plane of MoS2 for hydrogen evolution

被引:658
作者
Tsai, Charlie [1 ,2 ]
Li, Hong [3 ,4 ]
Park, Sangwook [3 ]
Park, Joonsuk [5 ]
Han, Hyun Soo [3 ]
Norskov, Jens K. [1 ,2 ]
Zheng, Xiaolin [3 ]
Abild-Pedersen, Frank [1 ,2 ]
机构
[1] Stanford Univ, Dept Chem Engn, SUNCAT Ctr Interface Sci & Catalysis, 443 Via Ortega, Stanford, CA 94305 USA
[2] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, 2575 Sand Hill Rd, Menlo Pk, CA 94305 USA
[3] Stanford Univ, Dept Mech Engn, 440 Escondido Mall, Stanford, CA 94305 USA
[4] Nanyang Technol Univ, Sch Mech & Aerosp Engn, Singapore 639798, Singapore
[5] Stanford Univ, Dept Mat Sci & Engn, 440 Escondido Mall, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
ACTIVE EDGE SITES; OXYGEN REDUCTION; MONOLAYER MOS2; CO2; REDUCTION; MOLYBDENUM; NANOSHEETS; CATALYSTS; ELECTROCATALYSIS; LAYERS;
D O I
10.1038/ncomms15113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recently, sulfur (S)-vacancies created on the basal plane of 2H-molybdenum disulfide (MoS2) using argon plasma exposure exhibited higher intrinsic activity for the electrochemical hydrogen evolution reaction than the edge sites and metallic 1T-phase of MoS2 catalysts. However, a more industrially viable alternative to the argon plasma desulfurization process is needed. In this work, we introduce a scalable route towards generating S-vacancies on the MoS2 basal plane using electrochemical desulfurization. Even though sulfur atoms on the basal plane are known to be stable and inert, we find that they can be electrochemically reduced under accessible applied potentials. This can be done on various 2H-MoS2 nanostructures. By changing the applied desulfurization potential, the extent of desulfurization and the resulting activity can be varied. The resulting active sites are stable under extended desulfurization durations and show consistent HER activity.
引用
收藏
页数:8
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