Microwave-assisted synthesis of carbon nanotubes threaded core-shell CoPx/Co-Nx-C@CNT and its performance as an efficient bifunctional oxygen catalyst for the rechargeable zinc-air battery

被引:40
作者
Wu, X. [1 ,2 ]
Chen, S. [1 ,3 ]
Feng, Y. [1 ,2 ]
Yuan, Q. [1 ,2 ]
Gao, J. [1 ,2 ]
Chen, Y. [1 ,2 ]
Huang, Y. [1 ,2 ]
He, Y. -B. [4 ]
Gan, W. [1 ,3 ]
机构
[1] Harbin Inst Technol Shenzhen, State Key Lab Adv Welding & Joining, Shenzhen 518055, Peoples R China
[2] Harbin Inst Technol Shenzhen, Sch Mat Sci & Engn, Shenzhen 518055, Peoples R China
[3] Harbin Inst Technol Shenzhen, Sch Sci, Shenzhen 518055, Peoples R China
[4] Tsinghua Univ, Engn Lab Next Generat Power & Energy Storage Batt, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
All-solid-state zinc-air battery; Bifunctional cathode catalyst; All-in-one phosphidation-carbonization synthesis; Co-N-x-C moieties; Cobalt phosphide; DOUBLE HYDROXIDE NANOSHEETS; COBALT PHOSPHIDE; EVOLUTION REACTION; HOLLOW POLYHEDRON; COP NANOCRYSTALS; POROUS CARBON; ELECTROCATALYSTS; REDUCTION; HYDROGEN; NITROGEN;
D O I
10.1016/j.mtphys.2019.100132
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of bifunctional cathode catalysts with advantages such as high activity, low cost, and high durability is highly desirable and challenging for zinc-air batteries (ZABs) in energy applications. In this work, a novel type of bifunctional catalyst (CoPx/Co-N-x-C@CNT) simultaneously effective for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) was prepared via a simplified all-in-one phosphorization-carbonization synthesis, which is distinctively different from the previously reported carbonization and postphosphorization route. With the integration of efficient catalytic factors such as Co-N-x-C-coordinated moieties, cobalt phosphide, graphitic carbon shells, as well as a supportive and conductive matrix, the as-prepared CoPx/Co-N-x-C@CNT exhibits high catalytic activity for ORR and OER in 0.1 M KOH, with an output positive onset potential of 0.92 V vs reversible hydrogen electrode (RHE) for ORR and a low potential of 1.69 V vs RHE at 10 mA cm(-2) for OER. Remarkably, the assembled liquid and all-solid-state ZAB based on the as-prepared CoPx/Co-N-x-C@CNT showed superior cycling performance than the results of its Pt/C-based counterparts and some recently reported cobalt phosphide-based ZABs. The good flexibility and reversibility of the all-solid-state ZAB also verified its feasibility in applications such as wearable electronics.
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页数:8
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