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离子共价有机框架修饰隔膜实现的温度自适应水系锌碘电池

Temperature-Adaptive Aqueous Zinc-Iodine Batteries Enabled by Ionic Covalent Organic Framework Modified Separator.

作者信息

Wang Yuyang, Qi Yiming, Bi Guoyu, Yin Weiliang, Zhang Wei

机构信息

School of Materials Science and Engineering, Anhui University of Technology, Ma'anshan 243002, China.

出版信息

J Phys Chem Lett. 2025 Jun 5;16(22):5515-5522. doi: 10.1021/acs.jpclett.5c01097. Epub 2025 May 27.

Abstract

Zinc-iodine batteries (ZIBs) face challenges, such as polyiodide shuttling, self-discharge, and temperature sensitivity. To overcome these issues, we developed a separator functionalized with an ionic covalent organic framework (COF@GF), which incorporates pyridine quaternary ammonium active sites. The COF@GF separator enhances ionic conductivity (13.9 mS cm) and Zn transference number (0.76), suppresses anode dendrite formation, and reduces self-discharge. In situ Raman spectroscopy and theoretical calculations show that COF's moderate electronic conductivity improves I/I conversion kinetics and enhances polyiodide adsorption through Lewis acid-base interactions, thus controlling redox chemistry and suppressing shuttle effects. COF@GF-modified ZIBs exhibit stable cycling for over 5000 cycles at 20 C and perform well across temperatures from -5 to 60 °C. At 0 °C, the battery retains 89.6% of its capacity over 10000 cycles, with a minimal decay rate of 0.001% per cycle, showcasing the potential of ionic COF materials for practical aqueous ZIB applications.

摘要

锌碘电池(ZIBs)面临着诸如多碘化物穿梭、自放电和温度敏感性等挑战。为了克服这些问题,我们开发了一种用离子共价有机框架功能化的隔膜(COF@GF),它包含吡啶季铵活性位点。COF@GF隔膜提高了离子电导率(13.9 mS cm)和锌迁移数(0.76),抑制了阳极枝晶的形成,并减少了自放电。原位拉曼光谱和理论计算表明,COF适度的电子电导率改善了I/I转换动力学,并通过路易斯酸碱相互作用增强了多碘化物的吸附,从而控制氧化还原化学并抑制穿梭效应。COF@GF修饰的ZIBs在20℃下可稳定循环超过5000次,并且在-5至60℃的温度范围内表现良好。在0℃时,电池在10000次循环中保持其容量的89.6%,每个循环的衰减率最小为0.001%,展示了离子COF材料在实际水系ZIB应用中的潜力。

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