Fabrication of Au₂₅(SG)₁₈–ZIF‐8 Nanocomposites: A Facile Strategy to Position Au₂₅(SG)₁₈ Nanoclusters Inside and Outside ZIF‐8

Abstract

Multifunctional composite materials are currently highly desired for sustainable energy applications. A general strategy to integrate atomically precise Au₂₅ (SG)₁₈ with ZIF-8 (Zn(MeIm)₂ , MeIm = 2-methylimidazole), is developed via the typical Zn-carboxylate type of linkage. Au₂₅ (SG)₁₈ are uniformly encapsulated into a ZIF-8 framework (Au₂₅ (SG)₁₈ @ZIF-8) by coordination-assisted self-assembly. In contrast, Au₂₅ (SG)₁₈ integrated by simple impregnation is oriented along the outer surface of ZIF-8 (Au₂₅ (SG)₁₈ /ZIF-8). The porous structure and thermal stability of these nanocomposites are characterized by N₂ adsorption-desorption isothermal analysis and thermal gravimetric analysis. The distribution of Au₂₅ (SG)₁₈ in the two nanocomposites is confirmed by electron microscopy, and the accessibility of Au₂₅ (SG)₁₈ is evaluated by the 4-nitrophenol reduction reaction. The as-prepared nanocomposites retain the high porosity and thermal stability of the ZIF-8 matrix, while also exhibiting the desired catalytic and optical properties derived from the integrated Au₂₅ (SG)₁₈ nanoclusters (NCs). Au₂₅ (SG)₁₈ @ZIF-8 with isolated Au₂₅ sites is a promising heterogenous catalyst with size selectivity imparted by the ZIF-8 matrix. The structural distinction between Au₂₅ (SG)₁₈ @ZIF-8 and Au₂₅ (SG)₁₈ /ZIF-8 determines their different emission features, and provides a new strategy to adjust the optical behavior of Au₂₅ (SG)₁₈ for applications in bioimaging and biotherapy.