Kim Sungin, Kwag Jimin, Machello Chiara, Kang Sungsu, Heo Junyoung, Reboul Cyril F, Kang Dohun, Kang Seulki, Shim Sangdeok, Park So-Jung, Kim Byung Hyo, Hyeon Taeghwan, Ercius Peter, Elmlund Hans, Park Jungwon
Center for Nanoparticle Research, Institute for Basic Science (IBS), Seoul 08826, Republic of Korea.
School of Chemical and Biological Engineering, and Institute of Chemical Processes, Seoul National University, Seoul 08826, Republic of Korea.
Nano Lett. 2021 Jan 27;21(2):1175-1183. doi: 10.1021/acs.nanolett.0c04873. Epub 2021 Jan 8.
Active sites and catalytic activity of heterogeneous catalysts is determined by their surface atomic structures. However, probing the surface structure at an atomic resolution is difficult, especially for solution ensembles of catalytic nanocrystals, which consist of heterogeneous particles with irregular shapes and surfaces. Here, we constructed 3D maps of the coordination number (CN) and generalized CN () for individual surface atoms of sub-3 nm Pt nanocrystals. Our results reveal that the synthesized Pt nanocrystals are enclosed by islands of atoms with nonuniform shapes that lead to complex surface structures, including a high ratio of low-coordination surface atoms, reduced domain size of low-index facets, and various types of exposed high-index facets. 3D maps of are directly correlated to catalytic activities assigned to individual surface atoms with distinct local coordination structures, which explains the origin of high catalytic performance of small Pt nanocrystals in important reactions such as oxygen reduction reactions and CO electro-oxidation.
多相催化剂的活性位点和催化活性由其表面原子结构决定。然而,以原子分辨率探测表面结构很困难,尤其是对于催化纳米晶体的溶液集合体,其由具有不规则形状和表面的异质颗粒组成。在这里,我们构建了亚3纳米铂纳米晶体单个表面原子的配位数(CN)和广义配位数()的三维图。我们的结果表明,合成的铂纳米晶体被形状不均匀的原子岛包围,这些原子岛导致了复杂的表面结构,包括低配位表面原子的高比例、低指数晶面的畴尺寸减小以及各种类型的暴露高指数晶面。的三维图与分配给具有不同局部配位结构的单个表面原子的催化活性直接相关,这解释了小铂纳米晶体在诸如氧还原反应和一氧化碳电氧化等重要反应中高催化性能的起源。