快离子导体
锂(药物)
离子
硼
化学
固溶体
中子衍射
差示扫描量热法
电解质
盐(化学)
硼酸锂
离子键合
离子电导率
合金
结晶学
化学物理
材料科学
物理化学
热力学
晶体结构
有机化学
医学
物理
电极
硼酸盐玻璃
内分泌学
作者
Wan Si Tang,Koji Yoshida,Alexei V. Soloninin,Roman V. Skoryunov,Olga A. Babanova,A.V. Skripov,Mirjana Dimitrievska,Vitalie Stavila,Shin‐ichi Orimo,Terrence J. Udovic
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2016-09-02
卷期号:1 (4): 659-664
被引量:180
标识
DOI:10.1021/acsenergylett.6b00310
摘要
Solid lithium and sodium closo-polyborate-based salts are capable of superionic conductivities surpassing even liquid electrolytes, but often only at above-ambient temperatures where their entropically driven disordered phases become stabilized. Here we show by X-ray diffraction, quasielastic neutron scattering, differential scanning calorimetry, NMR, and AC impedance measurements that by introducing "geometric frustration" via the mixing of two different closo-polyborate anions, namely, 1-CB9H10– and CB11H12–, to form solid-solution anion-alloy salts of lithium or sodium, we can successfully suppress the formation of possible ordered phases in favor of disordered, fast-ion-conducting alloy phases over a broad temperature range from subambient to high temperatures. This result exemplifies an important advancement for further improving on the remarkable conductive properties generally displayed by this class of materials and represents a practical strategy for creating tailored, ambient-temperature, solid, superionic conductors for a variety of upcoming all-solid-state energy devices of the future.
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