多硫化物
碲
钴
催化作用
硫黄
锂(药物)
材料科学
空位缺陷
无机化学
调解人
化学
物理化学
结晶学
冶金
有机化学
电解质
电极
医学
内科学
内分泌学
作者
Qianhong Gong,Dawei Yang,Huiping Yang,Konglin Wu,Jie Zhang,Wei Bi,Jiefeng Diao,Canhuang Li,Jing Yu,Chaoyue Zhang,Mengyao Li,Graeme Henkelman,Jordi Arbiol,Qiaobao Zhang,Andreu Cabot
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-10-03
卷期号:18 (41): 28382-28393
被引量:23
标识
DOI:10.1021/acsnano.4c11068
摘要
The commercialization of lithium-sulfur batteries (LSBs) faces significant challenges due to persistent issues, such as the shuttle effect of lithium polysulfides (LiPSs) and the slow kinetics of cathodic reactions. To address these limitations, this study proposes a vacancy-engineered cobalt ditelluride catalyst (v-CoTe2) supported on nitrogen-doped carbon as a sulfur host at the cathode. Density functional theory calculations and experimental results indicate that the electron configuration modulation of v-CoTe2 enhances the chemical affinity and catalytic activity toward LiPS. Specifically, v-CoTe2 can strongly interact with PSs through multisite coordination, effectively facilitating the kinetics of the LiPS redox reaction. Furthermore, the introduction of Te vacancies generates a large number of spin-polarized electrons, further enhancing the reaction kinetics of LiPS. As a result, the v-CoTe2@S cathode demonstrates high initial capacity and excellent cyclic stability, maintaining 80.4% capacity after 500 cycles at a high current rate of 3 C. Even under a high sulfur load of 6.7 mg cm-2, a high areal capacity of 6.1 mA h cm-2 is retained after 50 cycles. These findings highlight the significant potential of Te vacancies in CoTe2 as a sulfur host material for LSBs.
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