双金属片
沸石咪唑盐骨架
材料科学
催化作用
咪唑酯
化学工程
吸附
多孔性
离子
金属有机骨架
配体(生物化学)
扩展X射线吸收精细结构
傅里叶变换红外光谱
无机化学
吸收光谱法
物理化学
化学
复合材料
有机化学
工程类
生物化学
受体
物理
量子力学
作者
Kyung‐Ryul Oh,Hyunjoon Lee,Gwang‐Nam Yun,Changho Yoo,Ji Woong Yoon,Ali Awad,Hyun-Wook Jeong,Young Kyu Hwang
标识
DOI:10.1021/acsami.2c20240
摘要
Bimetallic zeolitic imidazolate frameworks (ZIFs) containing two different metal ions can exhibit superior performances when applied in heterogeneous catalysis. Herein, we present a facile one-pot synthesis method for PdCo-ZIFs with various Pd/Co ratios, where Pd(II) ions are successfully incorporated into the Co node sites of the ZIF structure. The local structure of the bimetallic ZIFs was comprehensively investigated by pore-structure, X-ray absorption fine structure, and in situ CO adsorption Fourier transform infrared analyses. The results demonstrated that the framework comprises different coordination geometries of Co (tetrahedral) and Pd (square planar) ions connected by the benzimidazolate ligand. Notably, the inherently nonporous, 2D Co-ZIF structure was transformed into a hierarchical porous structure, and the PdCo-ZIFs exhibited a significantly increased concentration of defects and distorted Co sites. Based on these results, the catalytic performances of the synthesized ZIFs in the cycloaddition of CO2 to epoxides were evaluated under a cocatalyst and solvent-free conditions. The PdCo-ZIFs exhibited significantly higher catalytic activity (maximum turnover frequency, TOF = 2501 h–1) than Co-ZIF (TOF = 65 h–1) and Pd-ZIF (no activity), which revealed that the undercoordinated Co sites with distorted structure are the active sites rather than the incorporated Pd ions. This study provides a facile one-pot method for synthesizing bimetallic ZIFs with mixed-coordination modes, hierarchical porous structures, and modified defect concentrations, which would expand the library of structurally diverse bimetallic ZIFs toward various applications.
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