摘要
Conventional photocatalysts face limitations in solar energy absorption and photocatalytic efficiency, hindering their practical applications in energy conversion and environmental remediation. Given that heat is a general promoter of catalytic reaction activity, we here developed hydrogenated hollow mesoporous WO3 spheres (WO3–x) as dual-functional photocatalysts. They can utilize ultraviolet–visible light for direct photocatalysis, while simultaneously harnessing the remaining near-infrared portion of the solar spectrum to achieve photothermal enhancement. Due to the photothermally improved activation of reactants and accelerated reaction kinetics, the developed WO3–x exhibited a 3-fold increase in CH4 production with 96% selectivity in CO2 photoreduction and a 10-fold enhancement in toluene degradation under full-spectrum irradiation, compared to pristine WO3. Moreover, even after 100 days of storage in air, WO3–x retained its excellent near-infrared photothermal conversion ability and sustained enhancement of reaction activity. These findings highlight the significant potential of photothermal catalysis for efficient solar energy utilization, further driving the development of near-infrared photothermal conversion materials and their application in sustainable energy conversion and environmental remediation.
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