尖晶石
材料科学
催化作用
电催化剂
氧化物
纳米颗粒
金属
晶体结构
电化学
化学工程
无机化学
纳米技术
物理化学
结晶学
化学
电极
冶金
有机化学
工程类
作者
Jiheon Kim,Wonjae Ko,Ji Mun Yoo,Vinod K. Paidi,Ho Yeon Jang,Michael Shepit,Jongmin Lee,Hogeun Chang,Hyeon Seok Lee,Jinwoung Jo,Byung Hyo Kim,Sung‐Pyo Cho,J. van Lierop,Dokyoon Kim,Kug‐Seung Lee,Seoin Back,Yung‐Eun Sung,Taeghwan Hyeon
标识
DOI:10.1002/adma.202107868
摘要
Multi-metal oxide (MMO) materials have significant potential to facilitate various demanding reactions by providing additional degrees of freedom in catalyst design. However, a fundamental understanding of the (electro)catalytic activity of MMOs is limited because of the intrinsic complexity of their multi-element nature. Additional complexities arise when MMO catalysts have crystalline structures with two different metal site occupancies, such as the spinel structure, which makes it more challenging to investigate the origin of the (electro)catalytic activity of MMOs. Here, uniform-sized multi-metal spinel oxide nanoparticles composed of Mn, Co, and Fe as model MMO electrocatalysts are synthesized and the contributions of each element to the structural flexibility of the spinel oxides are systematically studied, which boosts the electrocatalytic oxygen reduction reaction (ORR) activity. Detailed crystal and electronic structure characterizations combined with electrochemical and computational studies reveal that the incorporation of Co not only increases the preferential octahedral site occupancy, but also modifies the electronic state of the ORR-active Mn site to enhance the intrinsic ORR activity. As a result, nanoparticles of the optimized catalyst, Co0.25 Mn0.75 Fe2.0 -MMO, exhibit a half-wave potential of 0.904 V (versus RHE) and mass activity of 46.9 A goxide-1 (at 0.9 V versus RHE) with promising stability.
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