Novel MOF-derived hollow CoFe alloy coupled with N-doped Ketjen Black as boosted bifunctional oxygen catalysts for Zn-air batteries

被引:63
作者
Ren, Shuangshuang [1 ]
Duan, Xinde [1 ]
Ge, Fayuan [1 ]
Chen, Zhijun [3 ]
Yang, Qingxiang [3 ]
Zhang, Mingdao [2 ]
Zheng, Hegen [1 ]
机构
[1] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
[2] Nanjing Univ Informat Sci & Technol, Sch Environm Sci & Engn, Jiangsu Key Lab Atmospher Environm Monitoring & P, Collaborat Innovat Ctr Atmospher Environm & Equip, Nanjing 210044, Peoples R China
[3] Zhengzhou Univ Light Ind, Sch Chem Engn & Mat Sci, Zhengzhou 450002, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks; Hollow CoFe alloys; Electrocatalysis; Zn-air batteries; CARBON NANOTUBES; ELECTROCATALYSTS; NANOPARTICLES; REDUCTION; HYBRID; OXIDES;
D O I
10.1016/j.cej.2021.131614
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Rational design of highly effcient bifunctional oxygen catalysts toward oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is a significant challenge for rechargeable Zn-air battery (ZAB). Herein, a newly developed hybrid catalyst (denoted as CoFe@NC/KB-800) consisting of hollow CoFe alloy and nitrogen-doped Ketjen Black is synthesized by pyrolysis of a novel Fe-glucosamine coated cobalt-based metal-organic framework. By virtue of ultra-high specific surface area of 1318.8 m(2) g(-1) and micro-/meso-/macropore structure, the optimal CoFe@NC/KB-800 catalyst exhibits a low reversible oxygen overpotential (Delta E) of 0.77 V between ORR and OER. Density functional theory (DFT) calculations validate that the superior catalytic activity is ascribed to synergistic CoFe@NC structure. Impressively, liquid ZAB catalyzed by CoFe@NC/KB-800 displays a high peak power density of 160 mW cm(-2)and a low voltage gap of 0.65 V after 600 cycles. Three all-solid-state ZABs in series can successfully light LED (similar to 2.2 V), displaying tremendous potentials in portable devices.
引用
收藏
页数:11
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