Achieving High-Performance Oxygen Reduction Catalyst and Zn-Air Battery through a Synergistic Nitrogen Doping Strategy

被引:5
|
作者
Zhu, Xiaoran [1 ,2 ]
Zhang, Jianze [3 ]
Wang, Yan [4 ]
Yang, Mingsheng [5 ]
Yu, Haiping [1 ,2 ]
Li, Tengfei [4 ]
Hu, Mingjun [5 ]
Yang, Jun [1 ,2 ,6 ]
机构
[1] Chinese Acad Sci, Beijing Inst Nanoenergy & Nanosyst, Beijing 101400, Peoples R China
[2] Univ Chinese Acad Sci, Sch Nanosci & Technol, Beijing 100049, Peoples R China
[3] Guangxi Univ, Sch Chem & Chem Engn, Ctr Nanoenergy Res, Nanning 530004, Peoples R China
[4] Guangxi Univ, Ctr Nanoenergy Res, Sch Phys Sci & Technol, Nanning 530004, Peoples R China
[5] Beihang Univ, Sch Mat Sci & Engn, Beijing 100191, Peoples R China
[6] Univ Elect Sci & Technol China, Shenzhen Inst Adv Study, Shenzhen 518000, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Fe-N-C; mesoporous structures; oxygen reduction reaction; synergistic N-doping; Zn-air batteries; METAL-FREE ELECTROCATALYSTS; MEMBRANE FUEL-CELLS; HYBRID FLOW BATTERY; DOPED CARBON; BIFUNCTIONAL ELECTROCATALYST; ORGANIC FRAMEWORKS; ACTIVE-SITES; HIGH-POWER; EFFICIENT; FE/N/C;
D O I
10.1002/ente.202200602
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
It remains a challenge to achieve high-performance, low-cost, and robustly durable Fe, N co-doped carbon-based oxygen reduction reaction (ORR) catalysts with abundantly accessible Fe-N-X sites. Herein, a novel scheme is designed to enrich the pore structure, increase the specific surface area, and generate spatially isolated Fe-N-X sites of the ORR catalyst, in which pyridine nitrogen-rich lamellar metal-organic complex (Fe-tetrapyridophenazine) is employed as the precursor and 2D graphitic carbon nitride (g-C3N4) as additional nitrogen source for achieving synergistic nitrogen-doping effect. The introduction of g-C3N4 not only ameliorates the nitrogen coordination environment of metal active centers of the composite, but also increases the specific surface area and improves the pore structure. The resultant Fe-NC&CN composite has abundant active sites as well as remarkable electrical conductivity and suitable pore size for electron transfer and reactant diffusion. As expected, the catalyst exhibits excellent ORR activity, driving the reaction with low overpotential (E-1/2 = 0.879 V) and remaining stable over a long reaction time (93% for 60 000 s), better than commercial Pt/C (20%) in all aspects. The assembled Zn-air battery exhibits high open-circuit voltage of 1.566 V and high specific capacity of 815 mAh g(Zn)(-1), as well as stable and persistent discharge performance.
引用
收藏
页数:12
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