Oxygen-Coordinated Cr Single-Atom Catalyst for Oxygen Reduction Reaction in Proton Exchange Membrane Fuel Cells

被引:10
作者
Luo, Junming [1 ]
Zhang, Yating [1 ]
Lu, Zhe [1 ]
Liu, Chao [2 ]
Xu, Yueshan [1 ]
Chen, Hui [1 ]
Wang, Qi [1 ]
Wu, Daoxiong [1 ]
Dang, Dai [2 ]
Deng, Yijie [3 ]
Rao, Peng [1 ]
Deng, Peilin [1 ]
Li, Jing [1 ]
Miao, Zhengpei [1 ]
Tian, Xinlong [1 ]
机构
[1] Hainan Univ, Sch Marine Sci & Engn, State Key Lab Trop Ocean Engn Mat & Mat Evaluat, Hainan Prov Key Lab Fine Chem, Haikou 570228, Peoples R China
[2] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
[3] Univ South China, Sch Resource Environm & Safety Engn, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金; 海南省自然科学基金;
关键词
fuel cells; oxygen reduction reaction; chromium; single-atom catalyst; electrocatalysis; CARBON;
D O I
10.1002/anie.202500500
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon-supported metal single-atom catalysts (M-SACs) are promising oxygen reduction reaction (ORR) catalysts. Their ORR activity and selectivity are significantly affected by the heteroatoms that coordinate the central metal atoms. Previous reports found that oxygen-coordinated M-SACs promoted a 2e- ORR rather than the 4e- ORR that is more desirable for fuel cells. Herein, we report for the first time that oxygen-coordinated M-SACs are capable of promoting the 4e- ORR in acid media. We prepared a Cr(acac)-NC catalyst with the central Cr atom coordinated by two O atoms. The Cr(acac)-NC catalyst not only exhibits excellent ORR activity and stability in acid media, but also delivers high proton exchange membrane fuel cell (PEMFC) performance comparable to N-coordinated M-SACs. Density functional theory (DFT) calculations reveal that Cr-O2 moieties located on the zigzag edge of the carbon support are the ORR-active sites.
引用
收藏
页数:9
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