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用于高能量密度柔性准固态水系电致变色电池的电致变色与能量存储解耦

Decoupling Electrochromism and Energy Storage for Flexible Quasi-Solid-State Aqueous Electrochromic Batteries with High Energy Density.

作者信息

Gao Kun, Ju Shidi, Li Shuning, Zhang Shaohua, Liu Jiajia, Yang Tian, Lv Jinsheng, Yu Wenjing, Zhang Zhipan

机构信息

Key Laboratory of Cluster Science, Ministry of Education of China, Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, P. R. China.

出版信息

ACS Nano. 2023 Sep 26;17(18):18359-18371. doi: 10.1021/acsnano.3c05702. Epub 2023 Sep 13.

Abstract

Currently, reported aqueous electrochromic batteries (ECBs) show only limited capacity with insufficient energy density and power density. Such a limitation is naturally imposed by the rationale that the cathode of ECBs stores charge by an ion intercalation/deintercalation mechanism, where the inherent inhibition of ion diffusion and structural collapse of cathode materials through repetitive charge/discharge cycles lead to low areal capacity and unsatisfactory electrochemical performance with short lifetime. Herein, we decouple the dual functions of electrochromism and energy storage in conventional cathodes of ECBs by introducing a polyaniline/triiodide composite cathode that is formed by direct electrolysis of an iodide-based quasi-solid-state aqueous electrolyte during charging. When paired with a zinc metal anode, the composite cathode can synergistically utilize the electrochromic property of polyaniline, the high-efficiency energy storage of the Zn-I system, as well as the effective anchorage of polyiodide by polyaniline to suppress the shuttle effect of triiodide. By selecting 1-butyl-3-methylimidazolium ion (BMI) as the cation, a liquid-solid cathode/quasi-solid-state electrolyte interface can be achieved to facilitate the interfacial charge transfer, rendering quasi-solid-state aqueous electrochromic batteries with a high areal capacity of 1363 μAh cm, energy density of 1650 μWh cm, and power density of 5186 μW cm.

摘要

目前,报道的水系电致变色电池(ECBs)仅表现出有限的容量,能量密度和功率密度不足。这种限制自然是由以下原理造成的:ECBs的阴极通过离子嵌入/脱嵌机制存储电荷,其中阴极材料在重复充放电循环中离子扩散的固有抑制和结构坍塌导致低面积容量和不令人满意的电化学性能以及短寿命。在此,我们通过引入聚苯胺/三碘化物复合阴极来分离ECBs传统阴极中电致变色和能量存储的双重功能,该复合阴极是在充电过程中通过对基于碘化物的准固态水系电解质进行直接电解形成的。当与锌金属阳极配对时,复合阴极可以协同利用聚苯胺的电致变色特性、Zn-I系统的高效能量存储以及聚苯胺对多碘化物的有效锚固作用来抑制三碘化物的穿梭效应。通过选择1-丁基-3-甲基咪唑鎓离子(BMI)作为阳离子,可以实现液-固阴极/准固态电解质界面以促进界面电荷转移,从而使准固态水系电致变色电池具有1363 μAh cm的高面积容量、1650 μWh cm的能量密度和5186 μW cm的功率密度。

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