插层(化学)
电解质
化学
无机化学
钠
溶剂
锂(药物)
电极
有机化学
物理化学
医学
内分泌学
作者
Jooha Park,Sung Joo Kim,Kyungmi Lim,Jiung Cho,Kisuk Kang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-10-04
卷期号:7 (10): 3718-3726
被引量:10
标识
DOI:10.1021/acsenergylett.2c01838
摘要
Titanium disulfide (TiS2), a first-generation cathode in lithium batteries, has also attracted a broad interest as a sodium-ion battery electrode due to fast sodium intercalation kinetics and large theoretical capacity. However, the reversibility of sodium de/intercalation is far inferior to that of lithium because of the unfavorable intermediate phase formation. Herein, we demonstrate that reconfiguring sodium intercalation via partial solvent cointercalation alters the phase-transition paths for the entire reactions of NaxTiS2 (0 < x < 1), detouring the formation of the unfavorable intermediates. Additionally, it unexpectedly results in a remarkable enhancement of sodium intercalation reversibility, boosting the cycle stability (1000 cycles) accompanying high power capability (10C rate). Comparative investigations reveal that the sodium intercalation in ether-based electrolyte involves a preintercalation of solvent molecules, which is subsequently dissimilar to the bare sodium intercalation in conventional electrolytes. Rediscovery of the intercalation behavior of TiS2 offers a new insight in revisiting the reversibility and kinetics of the commonly known electrodes for batteries.
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