Center of Advanced Nanocatalysis (CAN-USTC), University of Science and Technology of China , Hefei, Anhui 230026, China.
Materials Characterization and Preparation Center (MCPC), Southern University of Science and Technology of China , Shenzhen, Guangdong 518055, China.
ACS Appl Mater Interfaces. 2017 Nov 15;9(45):39450-39455. doi: 10.1021/acsami.7b14134. Epub 2017 Nov 1.
Herein, a series of carbocatalysts containing Ru-based clusters have been prepared by the assistance of zeolite-imidazolate frameworks (ZIFs). The introduction of Ru is based on the adsorption of well-defined Ru(CO) within the cavity of ZIFs following decomposition at 900 °C. Moreover, without breaking the skeleton and porosity of ZIFs, the as-generated Ru species would bond with the Co nodes in situ to form bimetallic Ru-Co clusters if the Co-bearing metal-organic frameworks were utilized as the host. Within the confined space of ZIFs, the assembly of Ru and Co could be rationally designed, and their structures could be sophisticatedly controlled at the atomic scale. Among these Ru-based compositions, the Ru-Co clusters@N-C exhibited remarkable catalytic activity for the NH decomposition to H and NH synthesis versus Ru-Co NPs@N-C, Ru clusters@N-C, and Ru NPs@N-C. This study may open up a new routine to synthesize metallic clusters or other subnano structures by the confinement of ZIFs.
本文通过沸石咪唑酯骨架(ZIFs)的辅助作用,制备了一系列含有 Ru 基簇的碳催化剂。Ru 的引入是基于在 900°C 下分解时,将具有明确结构的 Ru(CO)吸附在 ZIFs 的空腔内。此外,如果使用含 Co 的金属有机骨架作为主体,则生成的 Ru 物种会在原位与 Co 节点结合,形成双金属 Ru-Co 簇,而不会破坏 ZIFs 的骨架和孔隙率。在 ZIFs 的受限空间内,可以合理设计 Ru 和 Co 的组装,并在原子尺度上对其结构进行复杂控制。在这些 Ru 基化合物中,Ru-Co 簇@N-C 对 NH 的分解表现出显著的催化活性,生成 H 和 NH 的反应优于 Ru-Co NPs@N-C、Ru 簇@N-C 和 Ru NPs@N-C。这项研究可能为通过 ZIFs 的限制来合成金属簇或其他亚纳米结构开辟了一条新途径。