Enhanced Photo‐Thermal CO2 Methanation with Tunable RuxNi1‐x Catalytic Sites: Alloying Beyond Pure Ru

Abstract Developing solid‐solution nano‐alloys from immiscible metals has garnered significant interest; however, the high formation entropy poses substantial challenges in synthesis, hindering a comprehensive understanding of the catalytic mechanisms under alloying effects. Herein, the synthesis of small‐sized (≈2.5 nm) Ru x Ni 1‐x solid‐solution alloy nanoparticles with precisely controlled Ru/Ni ratios across a broad compositional range is reported for the first time, despite their bulk immiscibility. The Ru 0.76 Ni 0.24 /TiO 2 catalyst, with an optimized Ru/Ni ratio, delivers superior photo‐thermal catalytic activity for CO 2 methanation, achieving a CH 4 production rate of 3.58 mol g metal −1 h −1 with 94% selectivity at 250 °C under light irradiation, representing a 2.82‐fold enhancement over monometallic Ru/TiO 2 . Comprehensive investigations reveal that the reconstruction of electronic structure at Ru–Ni active sites enhances the adsorption/activation of reactants, promotes the transformation of intermediate HCO 3 * to HCOO * , and facilitates the separation of the photo‐generated charge carriers witnessed by the femtosecond time‐resolved transient absorption (fs‐TA) spectroscopy. These combined effects collectively result in significantly enhanced CH 4 formation performance. This work highlights the potential of regulating catalytic sites in immiscible metal combinations for photo‐thermal catalytic CO 2 conversion, underscoring the promise of these cost‐effective alloys in heterogeneous catalysis.