Lihua Zhu*, Yilun Sun, Huaze Zhu, Guoliang Chai*, Zhiqing Yang*, Congxiao Shang, Hengqiang Ye, Bing Hui Chen, Anna Kroner and Zhengxiao Guo*,
{"title":"铂单原子和簇在(Ni,Co)(OH)2底物上的有效系综催化高选择性、高效和稳定的加氢反应","authors":"Lihua Zhu*, Yilun Sun, Huaze Zhu, Guoliang Chai*, Zhiqing Yang*, Congxiao Shang, Hengqiang Ye, Bing Hui Chen, Anna Kroner and Zhengxiao Guo*, ","doi":"10.1021/acscatal.2c01901","DOIUrl":null,"url":null,"abstract":"<p >A Pt–Ni–Co catalyst was synthesized with Pt single atoms and atomic clusters (SAACs) dispersed over (Ni,Co)(OH)<sub>2</sub> 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 (H<sub>2</sub> ∼ 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 −NO<sub>2</sub> and the Pt clusters adsorbing and homolytically dissociating H<sub>2</sub> molecules, and the H species then readily move to the adsorbed −NO<sub>2</sub> group, overcoming a much reduced energy barrier on the (Ni,Co)(OH)<sub>2</sub>, 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 −NO<sub>2</sub> or other easily hydrogenated groups (such as C═C, C≡N, and C═O).</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"12 13","pages":"8104–8115"},"PeriodicalIF":11.3000,"publicationDate":"2022-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":"{\"title\":\"Effective Ensemble of Pt Single Atoms and Clusters over the (Ni,Co)(OH)2 Substrate Catalyzes Highly Selective, Efficient, and Stable Hydrogenation Reactions\",\"authors\":\"Lihua Zhu*, Yilun Sun, Huaze Zhu, Guoliang Chai*, Zhiqing Yang*, Congxiao Shang, Hengqiang Ye, Bing Hui Chen, Anna Kroner and Zhengxiao Guo*, \",\"doi\":\"10.1021/acscatal.2c01901\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A Pt–Ni–Co catalyst was synthesized with Pt single atoms and atomic clusters (SAACs) dispersed over (Ni,Co)(OH)<sub>2</sub> 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 (H<sub>2</sub> ∼ 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 −NO<sub>2</sub> and the Pt clusters adsorbing and homolytically dissociating H<sub>2</sub> molecules, and the H species then readily move to the adsorbed −NO<sub>2</sub> group, overcoming a much reduced energy barrier on the (Ni,Co)(OH)<sub>2</sub>, 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 −NO<sub>2</sub> or other easily hydrogenated groups (such as C═C, C≡N, and C═O).</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"12 13\",\"pages\":\"8104–8115\"},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2022-06-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.2c01901\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscatal.2c01901","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Effective Ensemble of Pt Single Atoms and Clusters over the (Ni,Co)(OH)2 Substrate Catalyzes Highly Selective, Efficient, and Stable Hydrogenation Reactions
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).
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.