| Literature DB >> 29962046 |
Mingzhen Hu1,2, Shu Zhao1,3, Shoujie Liu4, Chen Chen1, Wenxing Chen1, Wei Zhu1, Chao Liang5, Weng-Chon Cheong1, Yu Wang1, Yi Yu5, Qing Peng1, Kebin Zhou2, Jun Li1, Yadong Li1.
Abstract
Controllable synthesis of ultrasmall atomically ordered intermetallic nanoparticles is a challenging task, owing to the high temperature commonly required for the formation of intermetallic phases. Here, a metal-organic framework (MOF)-confined co-reduction strategy is developed for the preparation of sub-2 nm intermetallic PdZn nanoparticles, by employing the well-defined porous structures of calcinated ZIF-8 (ZIF-8C) and an in situ co-reduction therein. HAADF-STEM, HRTEM, and EDS characterizations reveal the homogeneous dispersion of these sub-2 nm intermetallic PdZn nanoparticles within the ZIF-8C frameworks. XRD, XPS, and EXAFS measurements further confirm the atomically ordered intermetallic phase nature of these sub-2 nm PdZn nanoparticles. Selective hydrogenation of acetylene evaluation results show the excellent catalytic properties of the sub-2 nm intermetallic PdZn, which result from the energetically more favorable path for acetylene hydrogenation and ethylene desorption over the ultrasmall particles than over larger-sized intermetallic PdZn as revealed by density functional theory (DFT) calculations. Moreover, this protocol is also extendable for the preparation of sub-2 nm intermetallic PtZn nanoparticles and is expected to provide a novel methodology in synthesizing ultrasmall atomically ordered intermetallic nanomaterials by rationally functionalizing MOFs.Entities:
Keywords: MOF-confined; intermetallics; sub-2 nm
Year: 2018 PMID: 29962046 DOI: 10.1002/adma.201801878
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849