Suppr超能文献

通过溶剂化结构工程实现宽电化学窗口的稀水-非质子混合电解质

Dilute Aqueous-Aprotic Hybrid Electrolyte Enabling a Wide Electrochemical Window through Solvation Structure Engineering.

作者信息

Wu Shuilin, Su Bizhe, Sun Mingzi, Gu Shuai, Lu Zhouguang, Zhang Kaili, Yu Denis Y W, Huang Bolong, Wang Pengfei, Lee Chun-Sing, Zhang Wenjun

机构信息

Department of Materials Science and Engineering, & Center of Super-Diamond and Advanced Films, City University of Hong Kong, 83 Tat Chee Avenue, Hong Kong, China.

School of Energy and Environment, City University of Hong Kong, 83 Tat Chee Avenue, Hong Kong, China.

出版信息

Adv Mater. 2021 Oct;33(41):e2102390. doi: 10.1002/adma.202102390. Epub 2021 Aug 31.

Abstract

The application of superconcentrated aqueous electrolytes has shown great potential in developing high-voltage electrochemical double-layer capacitors (EDLCs). However, the broadening of the electrochemical window of such superconcentrated electrolytes is at the expense of their high cost, low ionic conductivity, high density, and narrow operating temperature range. Herein, the electrochemical window of water (>3 V) at low salt concentration (3 m) is expanded by using an aprotic solvent, i.e., trimethyl phosphate (TMP), to regulate the solvation structure of the electrolyte. Benefiting from the low salt concentration, such electrolyte is simultaneously featured with high ionic conductivity, low density, and wide temperature compatibility. Based on the dilute hybrid electrolyte, EDLCs constructed by using porous graphene electrodes are able to operate within an enlarged voltage range of 0-2.4 V at a wide range of temperatures from -20 to 60 °C. They also present excellent rate capability and cycle stability, i.e., 83% capacitance retention after 100 000 cycles. Density functional theory calculations verify that TMP induces a significant electronic modulation for the bonding environment of the electrolyte. This enables the stronger binding of Na -H O with freely migrating TMP to expand the voltage window to exceed the potential limitation of aqueous electrolytes.

摘要

超浓水电解质在开发高压电化学双层电容器(EDLC)方面已显示出巨大潜力。然而,此类超浓电解质电化学窗口的拓宽是以其高成本、低离子电导率、高密度和窄工作温度范围为代价的。在此,通过使用非质子溶剂,即磷酸三甲酯(TMP)来调节电解质的溶剂化结构,在低盐浓度(3 m)下扩大了水的电化学窗口(>3 V)。受益于低盐浓度,这种电解质同时具有高离子电导率、低密度和宽温度兼容性。基于稀混合电解质,使用多孔石墨烯电极构建的EDLC能够在-20至60°C的宽温度范围内,在0-2.4 V的扩大电压范围内运行。它们还具有出色的倍率性能和循环稳定性,即在100000次循环后电容保持率为83%。密度泛函理论计算证实,TMP对电解质的键合环境产生了显著的电子调制。这使得Na-H₂O与自由迁移的TMP之间的结合更强,从而扩大了电压窗口,超过了水电解质的电位限制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验