构建 ZnTe-CoTe2 异质结构,提高锂硫电池的长循环性能

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY Electrochimica Acta Pub Date : 2024-07-02 DOI:10.1016/j.electacta.2024.144648
Congying Fang, Ran Liu, Xiaokang Tan, Mengying Zhang, Yinzhuang Fang, Xiaolong Yan, Aiping Zhang, Xianbao Wang, Tao Mei
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引用次数: 0

摘要

采用模板辅助法合成了一种双金属 ZnTe-CoTe2 异质结构,并将其支撑在掺杂 N 的碳框架(NC)上,作为锂硫电池(LSB)的硫宿主。NC结构不仅能为离子/电子的快速传输建立高效的导电通道,还能通过多重空间限制抑制多硫化物的穿梭。此外,ZnTe-CoTe2 异质界面的构建削弱了 Li2S 的成核/分解障碍,促进了硫的双向转化。得益于上述优点,组装电池在 0.2 摄氏度时可提供 1250 mAh g-1 的高初始放电容量,并实现了更高的长循环性能,在 1000 次循环后,1 摄氏度时的衰减率为 0.047%。此外,即使在硫负荷为 4 mg cm-2 和 E/S 比率为 6 μL mg-1 的情况下,面积容量也能达到 3 mAh cm-2。
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Constructing ZnTe-CoTe2 heterostructures for enhanced long cycling performance of lithium-sulfur batteries

A type of bimetallic ZnTe-CoTe2 heterostructure was synthesized adopting template-assisted method which was supported on N-doped carbon framework (NC) to serve as sulfur host for lithium sulfur batteries (LSBs). The NC structure not only could build efficient conductive channels for fast ion/electron transport, but also inhibit the polysulfides shuttling via multiple spatial confinement. Besides, the construction of ZnTe-CoTe2 heterogeneous interface weakened the nucleation/decomposition barrier of Li2S and promoted the bidirectional conversion of sulfur. Benefiting from the advantages mentioned above, therefore, the assembled batteries delivered a high initial discharge capacity of 1250 mAh g-1 at 0.2 C and achieved enhanced long cycling performance with an attenuation rate of 0.047% at 1 C after 1000 cycles. Furthermore, even under sulfur loading of 4 mg cm-2 and E/S ratio of 6 μL mg-1, the area capacity could also reach to 3 mAh cm−2.

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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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