| Literature DB >> 30650222 |
Yiming Niu1,2, Xi Liu3,4, Yongzhao Wang1,2, Song Zhou3,4,5, Zhengang Lv3,4, Liyun Zhang1, Wen Shi1,2, Yongwang Li3,4, Wei Zhang6, Dang Sheng Su1, Bingsen Zhang1.
Abstract
Controllable synthesis of well-defined supported intermetallic catalysts is desirable because of their unique properties in physical chemistry. To accurately pinpoint the evolution of such materials at an atomic-scale, especially clarification of the initial state under a particular chemical environment, will facilitate rational design and optimal synthesis of such catalysts. The dynamic formation of a ZnO-supported PdZn catalyst is presented, whereby detailed analyses of in situ transmission electron microscopy, electron energy-loss spectroscopy, and in situ X-ray diffraction are combined to form a nanoscale understanding of PdZn phase transitions under realistic catalytic conditions. Remarkably, introduction of atoms (H and Zn in sequence) into the Pd matrix was initially observed. The resultant PdHx is an intermediate phase in the intermetallic formation process. The evolution of PdHx in the PdZn catalyst initializes at the PdHx /ZnO interfaces, and proceeds along the PdHx ⟨111⟩ direction.Entities:
Keywords: EELS; PdHx; PdZn intermetallics; heterogeneous catalysis; in situ TEM
Year: 2019 PMID: 30650222 DOI: 10.1002/anie.201812292
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336