Halide perovskite materials have shown immense potential
for photovoltaics
and photocatalytic CO2 reduction as a result of their excellent
optoelectronic properties. However, the rational way to directly apply
these materials to photoelectrochemical (PEC) CO2 reduction
remains unclear. Herein, on the basis of stepwise optimized interface-engineering
strategies, we synthesize CsPbBr3 (CPB) thin-film photocathode
catalysts using a two-step spin-coating method and modify the perovskites
with synergizing 5% fluorine (F) doping, Nafion (N) solution, and
15 nm Au coating, sequentially. It is demonstrated that, with the
synergistic effect of the interface-engineering approaches, the optimal
photocathode (CPB–F–N–Au) achieves greatly enhanced
light absorption and charger transfer capability compared to the pristine
CPB-based photocathode. As a result, the as-fabricated CPB–F–N–Au
photocathode exhibits the maximum photocurrent of −0.23 mA
cm–2 at a bias of −0.5 V versus E
Ag/AgCl under the 4.13 mW cm–2 light
illumination, which is twice that of the pristine CPB device. This
work demonstrates the practicability of directly applying halide perovskites
into PEC CO2 reduction and proposes useful interface-engineering
strategies for tuning the relevant device performance, which can also
be extended to other fields, like photovoltaics and photodetectors.