Zhu Guihua, Yang Haoyu, Jiang Ying, Sun Ziqi, Li Xiaopeng, Yang Jianping, Wang Haifeng, Zou Rujia, Jiang Wan, Qiu Pengpeng, Luo Wei
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Institute of Functional Materials, Donghua University, Shanghai, 201620, China.
School of Chemistry and Physics, Centre for Materials Science, Queensland University of Technology (QUT), Brisbane, QLD, 4000, Australia.
Adv Sci (Weinh). 2022 May;9(15):e2200394. doi: 10.1002/advs.202200394. Epub 2022 Mar 24.
The development of highly efficient and stable oxygen reduction electrocatalysts and revealing their underlying catalytic mechanism are crucial in expanding the applications of metal-air batteries. Herein, an excellent FeCo alloy nanoparticles (NPs)-decorated N-doped mesoporous carbon electrocatalyst (FeCo/NC) for oxygen reduction reaction, prepared through the pyrolysis of a dual metal containing metal-organic framework composite scaffold is reported. Benefiting from the highly exposed bimetal active sites and the carefully designed structure, the Fe Co /NC-800 catalyst exhibits a promising electrocatalytic activity and a superior durability, better than those of the state-of-the-art catalysts. Suggested by both the X-ray absorption fine structures and the density functional theoretical calculation, the outstanding catalytic performance is originated from the synergistic effects of the bimetallic loading in NC catalysts, where the electronic modulation of the Co active sites from the nearby Fe species leads to an optimized binding strength for reaction intermediates. This work demonstrates a class of highly active nonprecious metals electrocatalysts and provides valuable insights into investigating the structure-performance relationship of transition metal-based alloy catalysts.
开发高效稳定的氧还原电催化剂并揭示其潜在的催化机制对于扩展金属空气电池的应用至关重要。在此,报道了一种通过热解含双金属的金属有机框架复合支架制备的用于氧还原反应的优异的铁钴合金纳米颗粒(NPs)修饰的氮掺杂介孔碳电催化剂(FeCo/NC)。得益于高度暴露的双金属活性位点和精心设计的结构,FeCo/NC-800催化剂表现出有前景的电催化活性和优异的耐久性,优于目前最先进的催化剂。X射线吸收精细结构和密度泛函理论计算均表明,出色的催化性能源于NC催化剂中双金属负载的协同效应,其中附近铁物种对钴活性位点的电子调制导致反应中间体的结合强度得到优化。这项工作展示了一类高活性非贵金属电催化剂,并为研究过渡金属基合金催化剂的结构-性能关系提供了有价值的见解。