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

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
Lihua Zhu*, Yilun Sun, Huaze Zhu, Guoliang Chai*, Zhiqing Yang*, Congxiao Shang, Hengqiang Ye, Bing Hui Chen, Anna Kroner and Zhengxiao Guo*, 
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引用次数: 13

摘要

将Pt单原子和原子簇(SAACs)分散在碳基体上的(Ni,Co)(OH)2纳米颗粒上,合成了Pt - Ni - Co催化剂,该催化剂在中等条件下(H2 ~ 1.0 MPa,≤40℃)对硝基芳烃的加氢反应具有较高的催化活性,转化率高达100%,选择性高。结果表明,Pt SAACs具有协同协调的系综效应,强极化的Pt单原子优先吸附- NO2,而Pt团簇则吸附并均解离H2分子,H物质很容易移动到被吸附的- NO2基团上,克服了(Ni,Co)(OH)2上的能量垒,使反应速率提高了约50倍。该方法不仅揭示了SAACs的协同系综催化机理,而且还提供了一种通过在多金属衬底上从单原子到原子团簇的电子微环境微调来开发高效选择性催化剂的策略。硝基芳烃的例子可以很容易地应用于其他含有- NO2或其他容易氢化基团(如C = C, C≡N和C = O)的物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effective Ensemble of Pt Single Atoms and Clusters over the (Ni,Co)(OH)2 Substrate Catalyzes Highly Selective, Efficient, and Stable Hydrogenation Reactions

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).

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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
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.
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