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全固态氟离子电池电极/电解质界面的速率决定过程

Rate-Determining Process at Electrode/Electrolyte Interfaces for All-Solid-State Fluoride-Ion Batteries.

作者信息

Zhang Datong, Nakano Hiroyuki, Yamamoto Kentaro, Tanaka Kenta, Yahara Tatsuma, Imai Kazuyuki, Mori Takuya, Miki Hidenori, Nakanishi Shinji, Iba Hideki, Watanabe Toshiki, Uchiyama Tomoki, Amezawa Koji, Uchimoto Yoshiharu

机构信息

Graduate School of Human and Environmental Studies, Kyoto University, Yoshida Nihonmatsu Cho, Sakyo, Kyoto 606-8501, Japan.

Office of Society-Academia Collaboration for Innovation, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.

出版信息

ACS Appl Mater Interfaces. 2021 Jun 30;13(25):30198-30204. doi: 10.1021/acsami.1c06947. Epub 2021 Jun 21.

Abstract

Developing high-performance solid electrolytes that are operable at room temperature is one of the toughest challenges related to all-solid-state fluoride-ion batteries (FIBs). In this study, tetragonal β-PbSnF, a promising solid electrolyte material for mild-temperature applications, was modified through annealing under various atmospheres using thin-film models. The annealed samples exhibited preferential growth and enhanced ionic conductivities. The rate-determining factor for electrode/electrolyte interface reactions in all-solid-state FIBs was also investigated by comparing β-PbSnF with representative fluoride-ion- and lithium-ion-conductive materials, namely, LaF, CeF, and LiLaZrO. The overall rate constant of the interfacial reaction, , which included both mass and charge transfers, was determined using chronoamperometric measurements and Allen-Hickling simulations. Arrhenius-type correlations between and temperature indicated that activation energies calculated from and ionic conductivities (σ) were highly consistent. The results indicated that the mass transfer (electrolyte-side fluoride-ion conduction) should be the rate-determining process at the electrode/electrolyte interface. β-PbSnF, with a large σ value, had a larger value than LiLaZrO. Therefore, it is hoped that the development of high-conductivity solid electrolytes can lead to all-solid-state FIBs with superior rate capabilities similar to those of all-solid-state Li-ion batteries.

摘要

开发可在室温下运行的高性能固体电解质是全固态氟离子电池(FIB)面临的最严峻挑战之一。在本研究中,使用薄膜模型在各种气氛下对四方相β-PbSnF(一种适用于温和温度应用的有前景的固体电解质材料)进行退火改性。退火后的样品表现出择优生长和增强的离子电导率。通过将β-PbSnF与代表性的氟离子和锂离子导电材料(即LaF、CeF和LiLaZrO)进行比较,还研究了全固态FIB中电极/电解质界面反应的速率决定因素。使用计时电流测量和Allen-Hickling模拟确定了包括质量和电荷转移的界面反应的总速率常数 。 与温度之间的Arrhenius型相关性表明,从 和离子电导率(σ)计算得到的活化能高度一致。结果表明,质量转移(电解质侧氟离子传导)应该是电极/电解质界面处的速率决定过程。具有较大σ值的β-PbSnF的 值比LiLaZrO大。因此,希望高电导率固体电解质的开发能够带来具有与全固态锂离子电池类似的优异倍率性能的全固态FIB。

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