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–x
S due to intrinsic Cu+ ion migration. Here, we utilize Cu+ migration to design
a stratified CdS-Cu2–x
S/MoS2 photocatalyst, in which CuI@MoS2 (CuI-intercalated within the MoS2 basal plane) is created
by Cu+ migration and intercalation to the adjacent MoS2 surface. The epitaxial vertical growth of the CuI@MoS2 nanosheets on the surface of one-dimensional core–shell
CdS-Cu2–x
S 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.
Sb-based lead-free double perovskite Cs2AgSbX6 (X = Cl, Br or I) quantum dots exhibiting excellent air stability and blue emission with photoluminescence quantum yields of 31.33% were synthesized firstly using surfactant-assisted method.
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