Converting CO2 into renewable
fuels by solar energy
has been considered an ideal strategy to mitigate the climate crisis
and address the fossil fuel depletion problem. However, severe charge
carrier recombination and sluggish interfacial reaction dynamics make
it a challenge to achieve high conversion efficiency. Herein, a unique
2D/2D step-scheme (S-scheme) photocatalyst of Bi2WO6/C3N4 (BWO/CN) is constructed by a facile
electrostatic self-assembly strategy. The ultrathin 2D/2D heterostructure
endowed the BWO/CN hybrid with abundant contact interfaces, short
charge-transport distance, and relatively more accessible reaction
sites. Besides, the differences of work function between CN and BWO
induced the formation of a built-in electric field, resulting in much
enhanced interfacial charge transfer/separation rates. As a result,
the optimized BWO/CN heterojunction exhibits significantly improved
photocatalytic performance toward CO2 reduction, which
is approximately 2.8-fold higher than that of its CN counterpart.
The accelerated S-scheme charge-transfer mechanism is systematically
corroborated by X-ray photoelectron spectroscopy, photo-irradiated
Kelvin probe force microscopy, and electron spin resonance. This research
may provide a facile protocol for the rational design of an S-scheme
face-to-face 2D/2D heterojunction for efficient CO2 conversion.