阴极
电化学
电解质
锌
阳极
电池(电)
分子
无机化学
材料科学
有机自由基电池
二甲氧基乙烷
普鲁士蓝
醌
化学
电极
化学工程
水溶液
有机化学
物理化学
功率(物理)
物理
量子力学
工程类
作者
Zirui Lin,Hua‐Yu Shi,Lin Lu,Xianpeng Yang,Wanlong Wu,Xiaoqi Sun
标识
DOI:10.1038/s41467-021-24701-9
摘要
Abstract Rechargeable aqueous zinc-organic batteries are promising energy storage systems with low-cost aqueous electrolyte and zinc metal anode. The electrochemical properties can be systematically adjusted with molecular design on organic cathode materials. Herein, we use a symmetric small molecule quinone cathode, tetraamino-p-benzoquinone (TABQ), with desirable functional groups to protonate and accomplish dominated proton insertion from weakly acidic zinc electrolyte. The hydrogen bonding network formed with carbonyl and amino groups on the TABQ molecules allows facile proton conduction through the Grotthuss-type mechanism. It guarantees activation energies below 300 meV for charge transfer and proton diffusion. The TABQ cathode delivers a high capacity of 303 mAh g −1 at 0.1 A g −1 in a zinc-organic battery. With the increase of current density to 5 A g −1 , 213 mAh g −1 capacity is still preserved with stable cycling for 1000 times. Our work proposes an effective approach towards high performance organic electrode materials.
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