Highly active CoP embedded in hollow nitrogen-doped carbon as an efficient bifunctional electrocatalyst for rechargeable zinc-air batteries

被引:4
作者
Gan, Lang [1 ,2 ]
Liu, Jincheng [1 ]
Han, Linhu [1 ]
Li, Jiawang [1 ]
Zhao, Jing [1 ]
Chen, Kang [1 ]
Jiang, Dapeng [1 ]
Ren, Yanjie [1 ]
机构
[1] Changsha Univ Sci & Technol, Sch Energy & Power Engn, Key Lab Efficient & Clean Energy Utilizat, Changsha 410111, Peoples R China
[2] Shenzhen Univ, Inst Microscale Optoelect, Int Collaborat Lab 2D Mat Optoelect Sci & Technol, Minist Educ, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
Bi-functional electrocatalysts; Zinc-air battery; CoP; Metal organic framework; OXYGEN-EVOLUTION REACTION; METAL-ORGANIC FRAMEWORKS; NICKEL PHOSPHIDE; WATER OXIDATION; CATALYST; IRON; COBALT; OXIDE;
D O I
10.1016/j.ijhydene.2023.09.197
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Aqueous zinc-air batteries provide a possibility to replace fossil fuels. However, developing bi-functional electrocatalysts with high activity, low-cost and environmental friendliness for zinc-air batteries remains a challenge. In this work, we report an efficient bifunctional electrocatalyst (H-CoP@NC) that is fabricated by phosphating a hollow metal organic framework (MOF) prepared using a self-template method. The H-CoP@NC exhibits a halfwave potential of 0.81V (vs. RHE) for the oxygen reduction reaction (ORR), and an overpotential of 390 mV for the oxygen evolution reaction (OER) at a current density of 10 mA cm-2. Remarkably, the H-CoP@NC assembled zinc-air battery possesses a voltage gap of 0.82 V at a current density of 50 mA cm-2, and the voltage gap increases by only 0.01 V after 730 continuous charge and discharge cycles. This excellent electrocatalytic activity for ORR and OER can be attributed to the hollow structure, which improves mass transport during the electrocatalytic reaction, and the synergistic effect between CoP and heteroatom doped carbon skeletons which provide a high density of exposed active sites.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1391 / 1399
页数:9
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