摘要
The simultaneous utilization of methane and carbon dioxide via dry reforming holds promise for sustainable syngas production, yet conventional thermocatalytic processes suffer from energy-intensive operation and catalyst deactivation. Here, we report a light-driven methane dry reforming strategy utilizing sinter-resistant nano-island alloys catalyst, which are dynamically evolved from partially oxidized NiIr nanoclusters anchored on TiO 2 under photoexcitation. In situ characterization reveals interfacial charge oscillations on the catalyst induce a support-Ni-Ir electron transfer pathway, stabilizing oxidized Ni linkages while electronically modulating surface Ir sites. This dual functionality promotes CH x O* intermediate formation, suppressing coking during 100-h operation under intermittent illumination. By decoupling photoelectric and photothermal contributions, we demonstrate that localized photogenerated electrons dominate balanced syngas production, whereas photothermal effects enhance molecular vibrations. The optimized catalyst achieves a syngas rate of 10841 mmol g cat -1 h -1 with 25.0% light-to-fuel efficiency, establishing a design paradigm for solar-driven alloy catalysts in greenhouse gas valorization.
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