| Literature DB >> 29507243 |
Yanyan Zhao1, Ke R Yang2, Zechao Wang3,4, Xingxu Yan5,6,7, Sufeng Cao8, Yifan Ye9, Qi Dong1, Xizi Zhang1, James E Thorne1, Lei Jin3, Kelly L Materna2, Antonios Trimpalis8, Hongye Bai1, Sirine C Fakra9, Xiaoyan Zhong4, Peng Wang5,6, Xiaoqing Pan7,10, Jinghua Guo9, Maria Flytzani-Stephanopoulos8, Gary W Brudvig11, Victor S Batista11, Dunwei Wang12.
Abstract
Atomically dispersed catalysts refer to substrate-supported heterogeneous catalysts featuring one or a few active metal atoms that are separated from one another. They represent an important class of materials ranging from single-atom catalysts (SACs) and nanoparticles (NPs). While SACs and NPs have been extensively reported, catalysts featuring a few atoms with well-defined structures are poorly studied. The difficulty in synthesizing such structures has been a critical challenge. Here we report a facile photochemical method that produces catalytic centers consisting of two Ir metal cations, bridged by O and stably bound to a support. Direct evidence unambiguously supporting the dinuclear nature of the catalysts anchored on α-Fe2O3 is obtained by aberration-corrected scanning transmission electron microscopy (AC-STEM). Experimental and computational results further reveal that the threefold hollow binding sites on the OH-terminated surface of α-Fe2O3 anchor the catalysts to provide outstanding stability against detachment or aggregation. The resulting catalysts exhibit high activities toward H2O photooxidation.Entities:
Keywords: STEM; catalyst; solar energy; spectroscopy; water splitting
Year: 2018 PMID: 29507243 PMCID: PMC5866603 DOI: 10.1073/pnas.1722137115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205