选择性
催化作用
基质(水族馆)
吸附
纳米颗粒
化学
分子
结晶学
材料科学
物理化学
纳米技术
有机化学
海洋学
地质学
作者
Lihua Zhu,Yilun Sun,Huaze Zhu,Guoliang Chai,Zhiqing Yang,Congxiao Shang,Hengqiang Ye,Bing Hui Chen,Anna Kroner,Zhengxiao Guo
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2022-06-22
卷期号:12 (13): 8104-8115
被引量:39
标识
DOI:10.1021/acscatal.2c01901
摘要
A Pt–Ni–Co catalyst was synthesized with Pt single atoms and atomic clusters (SAACs) dispersed over (Ni,Co)(OH)2 nanoparticles on a carbon matrix, which leads to high catalytic activity, up to 100% conversion, and selectivity in the hydrogenation of nitroaromatics under moderate conditions (H2 ∼ 1.0 MPa and ≤40 °C). A synergistically coordinated ensemble effect of the Pt SAACs is identified with the strongly polarized Pt single atoms preferentially adsorbing the −NO2 and the Pt clusters adsorbing and homolytically dissociating H2 molecules, and the H species then readily move to the adsorbed −NO2 group, overcoming a much reduced energy barrier on the (Ni,Co)(OH)2, enhancing the reaction rate by ca. 50 times. The approach not only reveals the coordinated ensemble catalysis mechanism of SAACs but also provides a strategy of developing highly efficient and selective catalysts by fine tuning of the electronic microenvironment from single atoms to atomic clusters co-located over a multimetallic substrate. The demonstrated case for nitroarenes can be readily applied for other species containing −NO2 or other easily hydrogenated groups (such as C═C, C≡N, and C═O).
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