A Binary Ionogel Electrolyte for the Realization of an All Solid-State Electrical Double-Layer Capacitor Performing at Low Temperature.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2024-11-11 Epub Date: 2024-06-28 DOI:10.1002/cssc.202400596
Emmanuel Pameté, Zhuanpei Wang, François Béguin
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引用次数: 0

Abstract

Over the last years, solid-state electrolytes made of an ionic liquid (IL) confined in a solid (inorganic or polymer) matrix, also known as ionogels, have been proposed to solve the leakage problems occurring at high temperatures in classical electrical double-layer capacitors (EDLCs) with an organic electrolyte, and thereof improve the safety. However, making ionogel-based EDLCs perform with reasonable power at low temperature is still a major challenge due to the high melting point of the confined IL. To overcome these limitations, the present contribution discloses ionogel films prepared in a totally oxygen/moisture-free atmosphere by encapsulating 70 wt % of an equimolar mixture of 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide and 1-ethyl-3-methylimidazolium tetrafluoroborate - [EMIm][BF4]0.5[FSI]0.5 - into a poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) network. The further called "binary ionogel" films demonstrated a high flexibility and a good ionic conductivity of 5.8 mS cm-1 at 20 °C. Contrary to the ionogels prepared from either [EMIm][FSI] or [EMIm][BF4], displaying melting at Tm=-16 °C and -7 °C, respectively, the crystallization of confined [EMIm][BF4]0.5[FSI]0.5 is quenched in the binary ionogel, which shows only a glass transition at -101 °C. This quenching enables an increased ionicity and ionic diffusion at the interface with the PVdF host network, leading the binary ionogel membrane to display higher ionic conductivity below -20 °C than the parent binary [EMIm][BF4]0.5[FSI]0.5 liquid. Laminate EDLCs were built with a 100 μm thick binary ionogel separator and electrodes made from a hierarchical micro-/mesoporous MgO-templated carbon containing a reasonable proportion of mesopores to enhance the mass transport of ions, especially at low temperature where the ionic diffusion noticeably decreases. The EDLCs operated up to 3.0 V with ideal EDL characteristics from -40 °C to room temperature. Their output specific energy under a discharge power of 1 kW kg-1 is ca. 4 times larger than with a cell implementing the same carbon electrodes together with the binary [EMIm][BF4]0.5[FSI]0.5 liquid. Hence, this binary ionogel electrolyte concept paves the road for developing safe and flexible solid-state energy storage devices operating at subambient temperatures in extreme environments.

用于实现低温下全固态双层电容器的二元离子凝胶电解质。
由离子液体(IL)封闭在固体基质中制成的固态电解质(也称为离子凝胶)已被提出用于防止双电层电容器(EDLC)的电解质泄漏,从而提高其安全性。然而,由于受限电解质的熔点较高,要使基于离子凝胶的双电层电容器在低温条件下以合理功率运行仍是一项重大挑战。为了克服这些限制,本论文披露了将 1-乙基-3-甲基咪唑鎓双(氟磺酰)亚胺和 1-乙基-3-甲基咪唑鎓四氟硼酸盐的二元混合物--[EMIm][BF4]0.5[FSI]0.5--封装到 PVdF-HFP 网络中制备的离子凝胶薄膜。由[EMIm][FSI]或[EMIm][BF4]制备的离子凝胶会出现冻结/熔化现象,与此相反,在二元离子凝胶中,封闭的[EMIm][BF4]0.5[FSI]0.5的结晶被淬灭,仅在-101 °C时出现玻璃化转变。这种淬火使得与 PVdF 主网络接口处的离子性和离子扩散增加,导致二元离子凝胶膜在 -20 °C 以下显示出比母体二元 [EMIm][BF4]0.5[FSI]0.5 液体更高的离子电导率。使用二元离子凝胶分离器和分层碳电极构建的层压式 EDLC 在-40 °C至室温范围内都能理想地运行,其输出能量是使用相同碳电极和二元[EMIm][BF4]0.5[FSI]0.5 离子液体的电池的约 4 倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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