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受光系统II启发的基于镍铁的电催化剂,通过第二配位层效应实现高效水氧化

Photosystem II Inspired NiFe-Based Electrocatalysts for Efficient Water Oxidation via Second Coordination Sphere Effect.

作者信息

Liu Ming, Li Na, Wang Xuemin, Zhao Jia, Zhong Di-Chang, Li Wei, Bu Xian-He

机构信息

School of Materials Science and Engineering, Nankai University, Tianjin, 300350, China.

State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China.

出版信息

Angew Chem Int Ed Engl. 2023 May 8;62(20):e202300507. doi: 10.1002/anie.202300507. Epub 2023 Apr 4.

Abstract

The mismatched fast-electron-slow-proton process in the electrocatalytic oxygen evolution reaction (OER) severely restricts the catalytic efficiency. To overcome these issues, accelerating the proton transfer and elucidating the kinetic mechanism are highly sought after. Herein, inspired by photosystem II, we develop a family of OER electrocatalysts with FeO /NiO units and carboxylate anions (TA ) in the first and second coordination sphere, respectively. Benefiting from the synergistic effect of the metal units and TA , the optimized catalyst delivers superior activity with a low overpotential of 270 mV at 200 mA cm and excellent cycling stability over 300 h. A proton-transfer-promotion mechanism is proposed by in situ Raman, catalytic tests, and theoretical calculations. The TA (proton acceptor) can mediate proton transfer pathways by preferentially accepting protons, which optimizes the O-H adsorption/activation process and reduces the kinetic barrier for O-O bond formation.

摘要

在电催化析氧反应(OER)中,快速电子与慢速质子不匹配的过程严重限制了催化效率。为克服这些问题,加速质子转移并阐明动力学机制备受关注。在此,受光系统II的启发,我们开发了一族OER电催化剂,其第一和第二配位球中分别含有FeO /NiO单元和羧酸根阴离子(TA )。受益于金属单元和TA 的协同效应,优化后的催化剂具有优异的活性,在200 mA cm 时过电位低至270 mV,并且在300 h以上具有出色的循环稳定性。通过原位拉曼光谱、催化测试和理论计算提出了一种质子转移促进机制。TA(质子受体)可通过优先接受质子来介导质子转移途径,从而优化O-H吸附/活化过程并降低O-O键形成的动力学势垒。

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