Rational design of nitrogen and fluorine co-doped metal-free porous carbons electrocatalysts for highly efficient oxygen reduction and zinc-air batteries

被引:0
|
作者
Li, Linqiang [1 ]
Qin, Na [1 ]
Ma, Huayun [1 ]
Liu, Jing [1 ]
Zhu, Zhiqiang [1 ]
Huo, Yaxiong [1 ]
Zhai, Lipeng [1 ]
Mi, Liwei [1 ,2 ]
机构
[1] Zhongyuan Univ Technol, Ctr Adv Mat Res, Henan Key Lab Funct Salt Mat, Zhengzhou 450007, Peoples R China
[2] Pingdingshan Univ, Sch Chem & Environm Engn, Pingdingshan 467000, Peoples R China
来源
CARBON NEUTRALITY | 2025年 / 4卷 / 01期
基金
中国国家自然科学基金;
关键词
Covalent organic frameworks; Nitrogen and fluorine co-doped; Metal-free electrocatalyst; Oxygen reduction reaction; Zinc-air batteries; COVALENT ORGANIC FRAMEWORKS; CRYSTALLINE; PERFORMANCE;
D O I
10.1007/s43979-024-00117-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The oxygen reduction reaction (ORR) is an important reaction in fuel cells and metal air batteries. The reaction is affected by slow kinetics and the use of high-priced and resource-scarce platinum-based catalysts. Therefore, there is an urgent need to develop cost-effective nonprecious metal catalysts for use in the ORR to replace Pt-based catalysts. In this study, we used two-dimensional covalent organic frameworks (recorded as TF-COFs) as precursors to produce a metal-free nitrogen and fluorine-co-doped porous carbon catalyst (recorded as TF-800, TF-900, TF-1000, and TF-1100). TF-1000 had a high initial potential (0.90 V) and half-wave potential (0.83 V) in an alkaline medium, indicating good catalytic activity. In addition, the ORR stability of TF-1000 was better than that of commercial Pt/C (20%). This is mainly because the porous carbon catalyst has a high specific surface area, and the nitrogen and fluorine atoms in it have good dispersion and synergistic effects on the polarization of adjacent carbon atoms. TF-1000 also shows excellent performance in zinc-air batteries. In the TF-1000 based zinc-air batteries, excellent battery performance was observed: the peak power density reached 216.66 mW<middle dot>cm-2, the specific capacity reached 752.86 mAh<middle dot>g-1 at 10 mA<middle dot>cm-2, and the long-term charge-discharge stability was demonstrated. This work provides inspiration for new strategies to prepare future ORR catalysts.
引用
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页数:10
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