While core-shell nanomaterials are highly desirable for realizing enhanced optical and catalytic properties, their synthesis with atomic-level control is challenging. Here, the synthesis and crystal structure of [Au₁₂ Ag₃₂ (SePh)₃₀ ]^4- , the first example of selenolated Au-Ag core-shell nanoclusters, comprising a gold icosahedron core trapped in a silver dodecahedron, which is protected by an Ag₁₂ (SePh)₃₀ shell, is presented. The gold core strongly modifies the overall electronic structure and induces synergistic effects, resulting in high enhancements in the stability and near-infrared-II photoluminescence. The Au₁₂ Ag₃₂ and its homometal analog Ag₄₄ , show strong interactions with oxygen vacancies of TiO₂ , facilitating the interfacial charge transfer for photocatalysis. Indeed, the Au₁₂ Ag₃₂ /TiO₂ exhibits remarkable solar H₂ production (6810 µmol g^-1 h^-1 ), which is ≈6.2 and ≈37.8 times higher than that of Ag₄₄ /TiO₂ and TiO₂ , respectively. Good stability and recyclability with minimal catalytic activity loss are additional features of Au₁₂ Ag₃₂ /TiO₂ . The experimental and computational results reveal that the Au₁₂ Ag₃₂ acts as an efficient cocatalyst by possessing a favorable electronic structure that aligns well with the TiO₂ bands for the enhanced separation of photoinduced charge carriers due to the relatively negatively charged Au₁₂ core. These atomistic insights will motivate uncovering of the structure-catalytic activity relationships of other nanoclusters.

Hyeseung Kim

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