CO2 conversion into valuable
chemicals and
fuels is
a sustainable route to the concurrent mitigation of the energy crisis
and the greenhouse effect. Herein, first principles calculations were
employed to study the photocatalytic CO2 reduction over
pristine WS2, S-vacancy WS2, and Pt cluster
loaded WS2. Our results indicate that the introducing of
S-vacancy and loading of Pt clusters can improve the optical absorption
in the visible-light region. Furthermore, S-vacancy can lower the
barrier (by about 0.17 eV) for *COOH intermediate formation. For Pt/WS2, the strong metal–support interaction is confirmed
by high adsorption energy and charge transfer. Importantly, the electron-rich
Pt cluster promotes *CO intermediates to facilitate the formation
of *CHO intermediates and to further protonate to CH4.
This study provides some useful insights into designing the catalysts
for the reduction of CO2 and further widens the applications
of WS2-based catalytic materials.