4.8 Article

MoS2-Stratified CdS-Cu2-xS Core-Shell Nanorods for Highly Efficient Photocatalytic Hydrogen Production

期刊

ACS NANO
卷 14, 期 5, 页码 5468-5479

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b09470

关键词

Cu-I@MoS2 catalytic and protective layers; femtosecond transient absorption; mapping surface charge distribution; photocatalytic water splitting; stratified CdS-Cu2-xS/MoS2

资金

  1. National Natural Science Foundation of China [21475021, 21427807, 21777096]
  2. Priority Academic Program Development of Jiangsu Higher Education Institutions
  3. Key Laboratory of Analytical Chemistry for Life Science [5431ZZXM1803]

向作者/读者索取更多资源

Heterojunction photocatalysts are widely adopted for efficient water splitting, but ion migration can seriously threaten the stability of heterojunctions, as with the well-known low stability of CdS-Cu2-xS due to intrinsic Cu+ ion migration. Here, we utilize Cu+ migration to design a stratified CdS-Cu2-xS/MoS2 photocatalyst, in which Cu-I@MoS2 (Cu-I-intercalated within the MoS2 basal plane) is created by Cu+ migration and intercalation to the adjacent MoS2 surface. The epitaxial vertical growth of the Cu-I@MoS2 nanosheets on the surface of one-dimensional core-shell CdS-Cu2-xS nanorods forms catalytic and protective layers to simultaneously enhance catalytic activity and stability. Charge transfer is verified by kinetics measurements with femtosecond time-resolved transient absorption spectroscopy and direct mapping of the surface charge distribution with a scanning ion conductance microscope. This design strategy demonstrates the potential of utilizing hybridized surface layers as effective catalytic and protective interfaces for photocatalytic hydrogen production.

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