Photocatalytic CO2 reduction
to renewable hydrocarbon
fuels is a promising strategy to address global energy issues; however,
producing fuels like CH4 is highly challenging under visible
light. In this work, fabrication of a two-dimensional bentonite (2D-Bt)
nanosheet mediated WO3/g-C3N4 Z-scheme
heterojunction for highly selective photocatalytic CO2 reduction
to CH4 under visible light has been investigated. The photocatalytic
performance of the newly developed WO3-embedded 2D pillared
Bt with 2D g-C3N4 composite for selective photocatalytic
CO2 reduction to methane was studied using H2O as the reducing agent under visible light. WO3/Bt/g-C3N4 (WBCN) exhibits the highest photocatalytic activity
for CH4 production, which was 6.01, 6.76, and 25.30 times
higher than using WO3/g-C3N4, Bt/g-C3N4, and g-C3N4 samples, respectively.
Noticeably, WO3-coupled with g-C3N4 was favorable for CO production; however, introducing Bt layered
clay was in favor of methane formation during the CO2 reduction
process. Additionally, the Z-scheme of the WO3/g-C3N4 composite with Bt as the electron moderator
could promote photoinduced charge separation and redox ability of
the separated charge carriers, resulting in excellent CO2 reduction to CH4. The rate of reaction was dependent
only on the external mass transfer due to surface reactions over the
WBCN composite catalyst. With increasing photon flux, methane production
was further enhanced due to the thermodynamically favorable process
for the activation of CO2 methanation reaction. Besides,
good cycling ability was observed due to the presence of a layered
clay structure, which was sustained in multiple cycles without obvious
deactivation. This study provides a green clay based noble-metal-free
approach to construct a structured composite photocatalyst with a
Z-scheme charge carrier and would be beneficial for CO2 reduction and other solar energy applications.