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二碲化钴与碲空位:一种高效催化剂,作为多功能多硫化物介质用于高性能锂硫电池。

Cobalt Ditelluride Meets Tellurium Vacancy: An Efficient Catalyst as a Multifunctional Polysulfide Mediator toward Robust Lithium-Sulfur Batteries.

作者信息

Gong Qianhong, Yang Dawei, Yang Huiping, Wu Konglin, Zhang Jie, Bi Wei, Diao Jiefeng, Li Canhuang, Yu Jing, Zhang Chao Yue, Li Mengyao, Henkelman Graeme, Arbiol Jordi, Zhang Qiaobao, Cabot Andreu

机构信息

Henan Key Laboratory of Quantum Materials and Quantum Energy, School of Quantum Information Future Technology, Henan University, Kaifeng 475004, China.

Catalonia Institute for Energy Research─IREC, Sant Adrià de Besòs, Barcelona 08930, Spain.

出版信息

ACS Nano. 2024 Oct 15;18(41):28382-28393. doi: 10.1021/acsnano.4c11068. Epub 2024 Oct 3.

Abstract

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-CoTe) 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-CoTe enhances the chemical affinity and catalytic activity toward LiPS. Specifically, v-CoTe 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-CoTe@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, a high areal capacity of 6.1 mA h cm is retained after 50 cycles. These findings highlight the significant potential of Te vacancies in CoTe as a sulfur host material for LSBs.

摘要

由于存在诸如多硫化锂(LiPSs)的穿梭效应和阴极反应动力学缓慢等持续性问题,锂硫电池(LSBs)的商业化面临重大挑战。为解决这些限制,本研究提出一种负载在氮掺杂碳上的空位工程碲化钴催化剂(v-CoTe)作为阴极的硫宿主。密度泛函理论计算和实验结果表明,v-CoTe的电子构型调制增强了对LiPS的化学亲和力和催化活性。具体而言,v-CoTe可通过多位点配位与多硫化物强烈相互作用,有效促进LiPS氧化还原反应的动力学。此外,碲空位的引入产生大量自旋极化电子,进一步增强了LiPS的反应动力学。结果,v-CoTe@S阴极表现出高初始容量和优异的循环稳定性,在3 C的高电流速率下500次循环后保持80.4%的容量。即使在6.7 mg cm的高硫负载下,50次循环后仍保留6.1 mA h cm的高面积容量。这些发现突出了CoTe中碲空位作为LSBs硫宿主材料的巨大潜力。

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