Developing highly efficient photocatalysts
to utilize solar radiation
for converting CO2 into solar fuels is of great importance
for energy sustainability and carbon neutralization. Herein, through
an alkali-etching-introduced interface reconstruction strategy, a
nanowire photocatalyst denoted as V–Bi19Br3S27, with rich Br and S dual-vacancies and surface Bi–O
bonding introduced significant near-infrared (NIR) light response,
has been developed. The as-obtained V–Bi19Br3S27 nanowires exhibit a highly efficient metallic
photocatalytic reduction property for converting CO2 into
CH3OH when excited solely under NIR light irradiation.
Free of any cocatalyst and sacrificial agent, metallic defective V–Bi19Br3S27 shows 2.3-fold higher CH3OH generation than Bi19Br3S27 nanowires. The detailed interfacial structure evolution and reaction
mechanism have been carefully illustrated down to the atomic scale.
This work provides a unique interfacial engineering strategy for developing
high-performance sulfur-based NIR photocatalysts for photon reducing
CO2 into alcohol for achieving high-value solar fuel chemicals,
which paves the way for efficiently using the solar radiation energy
extending to the NIR range to achieve the carbon neutralization goal.