阴极
水溶液
电化学
材料科学
化学工程
电导率
锌
电极
多孔性
电池(电)
导电体
无机化学
化学
复合材料
冶金
有机化学
物理化学
功率(物理)
物理
量子力学
工程类
作者
Cong Li,Chunman Zheng,Haolong Jiang,Shuxin Bai,Jinhao Jia
标识
DOI:10.1016/j.jallcom.2021.160587
摘要
• Hydrogen bonding network is responsible for the electrical conductivity of MOFs. • Ni-PTA-Mn has better discharge capacity and cycle stability than Ni-PTA. • Pseudo capacitance controlling mechanism plays a leading role in electrode reaction. Aqueous zinc-ion batteries are regarded as a novel scheme for the next generation of functional batteries due to their high safety and environment-friendly performance. Nevertheless, aqueous zinc-ion batteries suffer from poor cycling stability, which is mainly due to the poor structural stability and distortion of the electrode materials during charging and discharging. Herein, Ni-PTA-Mn, an organic metal framework porous material with a large specific surface area and conductive function, was directly synthesized by one-step hydrothermal method. When it was directly applied as the cathode of aqueous zinc-ion batteries, the batteries exhibited a discharge specific capacity of up to 139 mAh g −1 (0.1 A g −1 ) and an capacity retention rate of about 93% at 1 A g −1 (after 100 cycles). Outstanding electrochemical performance was mainly attributed to proton conductivity through the formation of H-bond networks inside the framework backbone.
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