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用于准固态钠离子电池的具有不可燃性和高离子导电性的 PYFSI 渗透的 SBA - 15 离子凝胶电解质

PYFSI-Infiltrated SBA-15 as Nonflammable and High Ion-Conductive Ionogel Electrolytes for Quasi-Solid-State Sodium-Ion Batteries.

作者信息

Gao Yongsheng, Chen Guanghai, Wang Xinran, Yang Haoyi, Wang Zhaohua, Lin Weiran, Xu Huajie, Bai Ying, Wu Chuan

机构信息

Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China.

Fundamental Industry Training Center, Tsinghua University, Beijing 100084, China.

出版信息

ACS Appl Mater Interfaces. 2020 May 20;12(20):22981-22991. doi: 10.1021/acsami.0c04878. Epub 2020 May 5.

Abstract

Exploring electrolytes of high safety is essential to pave the practical route for sodium-ion batteries (SIBs) toward their important applications in large-scale energy storage and power supplies. In this regard, ionogel electrolytes (IEs) have been highlighted owing to their high ionic conductivity, prominent electrochemical and thermal stability, and, more crucially, high interfacial wettability. However, present studies lack an understanding of the interaction of IEs, which determines the ion desolvation and migration. In this article, IEs comprising an SBA-15 host, an ionic liquid, sodium salt, and poly(vinylidene fluoride)-hexafluoro propylene (PVDF-HFP) have been proposed by mechanical ball milling and roller pressing. The component ratio has been optimized based on the balance between ionic conductivity and self-supporting capability of IEs. The optimal IEs showed sufficiently high ionic conductivity (2.48 × 10 S cm at 30 °C), wide electrochemical window (up to 4.8 V vs Na/Na), and high Na transference number (0.37). Due to the presence of SBA-15 and an ionic liquid, the IEs exhibited much improved thermal resistance than that of the conventional organic liquid electrolytes (OLEs). Furthermore, Fourier transform infrared (FT-IR) spectroscopy revealed the hydrogen bonding interaction between silanols and the dissolved salts, not only anchoring anions for immobilization but also promoting the dissociation of sodium salts. After being matched with the NaV(PO) (NVP) cathode and metallic Na anode, the SIBs presented a specific discharge capacity of up to 110.7 mA h g initially at room temperature with 92% capacity retention after 300 cycles. The improved safety and electrochemical performance provided insights into rationally regulating IEs and their interactions with the prospect of strengthening their practical applications in SIBs.

摘要

探索具有高安全性的电解质对于为钠离子电池(SIBs)在大规模储能和电源等重要应用中开辟实用路线至关重要。在这方面,离子凝胶电解质(IEs)因其高离子电导率、出色的电化学和热稳定性,以及更关键的高界面润湿性而备受关注。然而,目前的研究缺乏对离子凝胶电解质相互作用的理解,而这种相互作用决定了离子去溶剂化和迁移。在本文中,通过机械球磨和辊压提出了一种由SBA - 15主体、离子液体、钠盐和聚偏氟乙烯 - 六氟丙烯(PVDF - HFP)组成的离子凝胶电解质。基于离子凝胶电解质的离子电导率和自支撑能力之间的平衡对其成分比例进行了优化。优化后的离子凝胶电解质表现出足够高的离子电导率(30℃时为2.48×10 S cm)、宽电化学窗口(相对于Na/Na高达4.8 V)和高Na迁移数(0.37)。由于SBA - 15和离子液体的存在,离子凝胶电解质表现出比传统有机液体电解质(OLEs)更好的耐热性。此外,傅里叶变换红外(FT - IR)光谱揭示了硅醇与溶解盐之间的氢键相互作用,不仅固定阴离子以使其 immobilization,还促进了钠盐的解离。与NaV(PO)(NVP)阴极和金属Na阳极匹配后,钠离子电池在室温下初始比放电容量高达110.7 mA h g,300次循环后容量保持率为92%。安全性和电化学性能的提升为合理调控离子凝胶电解质及其相互作用提供了见解,有望加强其在钠离子电池中的实际应用。 (原文中“2.48 × 10 S cm”表述有误,推测可能是“2.48 × 10⁻³ S cm”之类,翻译时按原文呈现)

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