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链-链协同水凝胶电解质调节锌离子去溶剂化以实现柔性锌离子混合电容器中稳定的阳极和高工作电压。

Chain-Chain Synergistic Hydrogel Electrolytes Regulate Zinc Ions Desolvation for Stabilized Anodes and High Operating Voltage in Flexible Zinc Ions Hybrid Capacitors.

作者信息

Zhang Hang, Wan Li, You Ziran, Liang Jianrong, Lei Da, Cui Yongyan

机构信息

College of Chemical Engineering and Materials Science, Tianjin University of Science and Technology, Tianjin, 300457, P.R. China.

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin, 300071, P.R. China.

出版信息

Angew Chem Int Ed Engl. 2025 Aug 4;64(32):e202507403. doi: 10.1002/anie.202507403. Epub 2025 Jun 10.

Abstract

To maximize the energy density output, the complementary charge storage mechanism of aqueous zinc ion hybrid capacitors (ZIHCs) is superior and advanced, but continuous water-induced side reactions and uncontrolled dendrite growth of zinc anodes remain challenging. Additionally, the optimization of the hydrogel electrolyte/electrode interface is necessary for the stability and kinetic reversibility of the flexible zinc-based energy storage device. Herein, the P(AM-SBMA) (copolymer of acrylamide AM and zwitterionic compound SBMA)/gelatin hydrogel electrolyte (PSG) with a special semi-interpenetrating network is designed based on the chain-chain synergistic regulation mechanism to regulate the desolvation of zinc ions and optimize the operating voltage of flexible ZIHCs and stabilize surface chemistry of zinc anode. The obtained PSG-5 hydrogel electrolyte widens the electrochemical stability windows (ESW) of the flexible ZIHC to 2.45 V and achieves high Zn transference number of 0.87 and highly reversible plating/stripping of the zinc anode. Furthermore, the corresponding flexible ZIHC exhibits a high operating voltage of 2.2 V and provides a favorable energy density of 117 Wh kg at a power density of 293 W kg. This work provides useful insights for the development of efficient, flexible ZIHCs by preparing hydrogel electrolytes capable of stabilizing zinc anodes and widening ESW.

摘要

为了最大化能量密度输出,水系锌离子混合电容器(ZIHC)的互补电荷存储机制具有优越性和先进性,但持续的水引发副反应以及锌负极不受控制的枝晶生长仍然具有挑战性。此外,对于柔性锌基储能装置的稳定性和动力学可逆性而言,优化水凝胶电解质/电极界面是必要的。在此,基于链-链协同调节机制设计了具有特殊半互穿网络的P(AM-SBMA)(丙烯酰胺AM与两性离子化合物SBMA的共聚物)/明胶水凝胶电解质(PSG),以调节锌离子的去溶剂化作用,优化柔性ZIHC的工作电压,并稳定锌负极的表面化学性质。所制备的PSG-5水凝胶电解质将柔性ZIHC的电化学稳定窗口(ESW)拓宽至2.45 V,实现了0.87的高锌迁移数以及锌负极的高度可逆镀覆/剥离。此外,相应的柔性ZIHC表现出2.2 V的高工作电压,在功率密度为293 W kg时提供了117 Wh kg的良好能量密度。这项工作通过制备能够稳定锌负极并拓宽ESW的水凝胶电解质,为高效、柔性ZIHC的发展提供了有益的见解。

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