Optimizing the coordination environment of active sites to enhance heterogeneous electrocatalytic performances

IF 20.3 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Coordination Chemistry Reviews Pub Date : 2024-10-02 DOI:10.1016/j.ccr.2024.216243
Yuhao Duan , Dehong Chen , Ruiyong Zhang , Yunmei Du , Lei Wang
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Abstract

The design of the structure and catalytic function of electrocatalysts is an important core technology to solve the energy crisis. To realize the construction of ideal electrocatalysts, it is necessary to understand the structure-activity relationship between the internal structure (physical structure, electronic structure, electrochemical structure, etc.) of the active sites in electrocatalysts and the heterogeneous electrocatalytic performance from a comprehensive perspective. Obviously, the internal structure of electrocatalysts mainly depends on the actual coordination environment of their active sites. Generally, the coordination environment of the active site covers many aspects, such as coordination number (C.N.), bonding type, steric hindrance, bond length and bond angle, density of active center, etc. By establishing a structure-activity relationship between the coordination environment and the heterogeneous electrocatalytic performance, the design of the ideal coordination environment model of the active site is guided. Moreover, according to the type of catalyst and the location of the active site, the appropriate coordination environment control strategies were proposed for the active site at the bulk catalyst, the heterointerface, the carrier, as well as the electrocatalytic reaction interface, respectively. In particular, the local coordination environment of electrocatalytic reaction interface, as an important factor that directly affects the electrocatalytic performance, is often neglected. Then, the visualization of the coordination environment of the active site is realized by electron microscopy, spectroscopy configuration and In-situ monitoring techniques. Finally, this work summarizes the optimization of the coordination environment for the heterogeneous electrocatalytic reaction, and puts forward personal perspectives on the current challenges. We believe that this work will achieve the directional construction of high-efficiency electrocatalysts guided by the coordination environment of active sites, pointing out the direction for developing new energy in the future.

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优化活性位点的配位环境以提高异相电催化性能
电催化剂的结构和催化功能设计是解决能源危机的重要核心技术。要实现理想电催化剂的构建,就必须从全面的角度认识电催化剂活性位点内部结构(物理结构、电子结构、电化学结构等)与异相电催化性能之间的构效关系。显然,电催化剂的内部结构主要取决于其活性位点的实际配位环境。一般来说,活性位点的配位环境包括配位数(C.N.)、成键类型、立体阻碍、键长和键角、活性中心密度等多个方面。通过建立配位环境与异相电催化性能之间的结构-活性关系,可以指导设计理想的活性位点配位环境模型。此外,根据催化剂的类型和活性位点的位置,分别提出了活性位点在块体催化剂、异质界面、载体以及电催化反应界面的相应配位环境控制策略。其中,电催化反应界面的局部配位环境作为直接影响电催化性能的重要因素,往往被忽视。因此,本研究首先介绍了电催化反应界面的配位环境,然后通过电子显微镜、光谱配置和原位监测技术实现了活性位点配位环境的可视化。最后,这项工作总结了异相电催化反应配位环境的优化,并对当前面临的挑战提出了个人观点。我们相信,这项工作将实现以活性位点配位环境为导向的高效电催化剂的定向构建,为未来开发新能源指明方向。
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来源期刊
Coordination Chemistry Reviews
Coordination Chemistry Reviews 化学-无机化学与核化学
CiteScore
34.30
自引率
5.30%
发文量
457
审稿时长
54 days
期刊介绍: Coordination Chemistry Reviews offers rapid publication of review articles on current and significant topics in coordination chemistry, encompassing organometallic, supramolecular, theoretical, and bioinorganic chemistry. It also covers catalysis, materials chemistry, and metal-organic frameworks from a coordination chemistry perspective. Reviews summarize recent developments or discuss specific techniques, welcoming contributions from both established and emerging researchers. The journal releases special issues on timely subjects, including those featuring contributions from specific regions or conferences. Occasional full-length book articles are also featured. Additionally, special volumes cover annual reviews of main group chemistry, transition metal group chemistry, and organometallic chemistry. These comprehensive reviews are vital resources for those engaged in coordination chemistry, further establishing Coordination Chemistry Reviews as a hub for insightful surveys in inorganic and physical inorganic chemistry.
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