Facile synthesis of nitrogen- and phosphorus-Co-doped porous carbon nanosheets embedded with FeP clusters for the oxygen reduction reaction using rechargeable zinc-air batteries

被引:4
作者
Kang, Yong-gang [1 ]
Yan, Peng [1 ]
Yang, Wen-wu [1 ]
Chen, Bing-bing [2 ]
机构
[1] Northwestern Polytech Univ, Inst Coll Mech & Elect Engn, Xian 710072, Shanxi, Peoples R China
[2] Nanjing Tech Univ, Inst Dept Energy Sci & Engn, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen reduction reaction; Doped catalyst; Zn-air battery; DFT calculation; TOTAL-ENERGY CALCULATIONS; ATOMICALLY DISPERSED FE; HOLLOW SPHERES; EFFICIENT; ELECTROCATALYSTS; CATALYSTS; DESIGN; NANOPARTICLES; HYBRID; IRON;
D O I
10.1016/j.jelechem.2022.116122
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
There is an urgent need to develop non-precious-metal electrocatalysts for the oxygen reduction reaction (ORR) to replace traditional noble-metal electrocatalysts in zinc-air batteries (ZAB). Herein, we describe the preparation of N-, P -co-doped iron-based porous carbon nanosheets formed by doping iron into N-, P -co-doped nanosheets. Due to its unique core-shell structure and the synergistic effect between active sites, the electrocatalyst (FP0.6@CNP1000) exhibits high ORR activity in alkaline solution, with a remarkable half-wave potential (0.852 V vs RHE), high current density (5.41 mA cm(-2)), good stability, and excellent methanol tolerance. The FP0.6@CNP1000 electrocatalyst can be used as the cathode in a ZAB, thereby catalyzing the ORR, which achieves an open-circuit potential of 1.455 V, peak power density of 80 mW cm(-2), and excellent cycling stability for over 58 h. Density functional theory (DFT) calculations reveal that the ORR active site consists of an Fe center linked to three adjacent P atoms, and that the strong interactions between the substrate and the FeP cluster contribute to the ORR capacity.
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页数:9
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