电化学窗口
电解质
计时安培法
介电谱
电化学
离子电导率
电池(电)
快离子导体
材料科学
分析化学(期刊)
离子
阴极
电极
带隙
化学
光电子学
循环伏安法
热力学
物理化学
有机化学
功率(物理)
色谱法
物理
作者
Travis Thompson,Seungho Yu,Logan Williams,Robert D. Schmidt,Regina García-Méndez,J. Wolfenstine,Jan L. Allen,Emmanouil Kioupakis,Donald J. Siegel,Jeff Sakamoto
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2017-01-23
卷期号:2 (2): 462-468
被引量:282
标识
DOI:10.1021/acsenergylett.6b00593
摘要
The recent discovery of fast ion-conducting solid electrolytes could enable solid-state and other advanced battery chemistries with higher energy densities and enhanced safety. In addition to high ionic conductivity, a viable electrolyte should also exhibit an electrochemical window that is wide enough to suppress undesirable electronic transport (i.e., self-discharge and/or short circuiting) arising from charge injection or extraction from the electrodes. Here, direct current chronoamperometry, alternating current electrochemical impedance spectroscopy, and optical absorption band gap measurements are combined with first-principles calculations to systematically characterize the electrochemical window of the promising superionic conductor Li7La3Zr2O12 (LLZO). Negligible electronic current was measured within LLZO for a wide range of voltages relevant for high-voltage cathodes. This auspicious behavior is consistent with both the large band gap (∼6 eV) predicted for LLZO and the absolute positions of its band edges. These features imply that a wide electrochemical window is an intrinsic property of LLZO, facilitating its use in next-generation batteries.
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