{"title":"CoTe2/Co─O─NC氧桥对稳定锂硫电池多硫化物吸附催化作用的增强","authors":"Zhao Yang, Rui Yan, Jingchen Han, Tong Wu, Qingsheng Wu, Guangfeng Wei, Yongqing Fu, Ming Wen","doi":"10.1002/adfm.202417834","DOIUrl":null,"url":null,"abstract":"Lithium–sulfur batteries are regarded as candidates for next-generation energy storage systems, but their slow reaction kinetics and shuttle effect severely hinder their practical applications. One of the key solutions is to design and apply efficient, highly stable, and long-life catalysts. Herein, a nanostructured CoTe<sub>2</sub>/Co─O─NC electrocatalytic material is developed to achieve effective adsorption and bidirectional catalytic conversions of lithium polysulfides (LiPSs). Results show that oxygen bridges (Co─O─C) formed in the CoTe<sub>2</sub>/Co─O─NC not only effectively shift d-band center of the cobalt near its Fermi level to enhance adsorption of LiPSs but also strengthen the built-in electric fields of CoTe<sub>2</sub>/Co heterojunctions to reduce energy barrier for sulfur conversion. Deposition and dissociation of Li<sub>2</sub>S are significantly enhanced during charging/discharging processes. Durability of highly active catalyst is significantly improved, and rapid cross-interfacial charge transfer is also achieved. The synthesized S/CoTe<sub>2</sub>/Co─O─NC cathode exhibits an initial capacity of 1498 mAh g<sup>−1</sup> at 0.1 C, and its decay rate of capacity over 500 cycles at 0.5 C is only 0.046%. Li─S pouch cells using the cathode show an energy density of 368 Wh kg<sup>−1</sup> and areal capacity of 7.7 mAh cm<sup>−2</sup> at a sulfur loading of 6.7 mg cm<sup>−2</sup>, with an electrolyte/sulfur ratio of 4 µL mg<sup>−1</sup>.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"52 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oxygen Bridges of CoTe2/Co─O─NC Enhancing Adsorption-Catalysis of Polysulfide for Stable Lithium–Sulfur Batteries\",\"authors\":\"Zhao Yang, Rui Yan, Jingchen Han, Tong Wu, Qingsheng Wu, Guangfeng Wei, Yongqing Fu, Ming Wen\",\"doi\":\"10.1002/adfm.202417834\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Lithium–sulfur batteries are regarded as candidates for next-generation energy storage systems, but their slow reaction kinetics and shuttle effect severely hinder their practical applications. One of the key solutions is to design and apply efficient, highly stable, and long-life catalysts. Herein, a nanostructured CoTe<sub>2</sub>/Co─O─NC electrocatalytic material is developed to achieve effective adsorption and bidirectional catalytic conversions of lithium polysulfides (LiPSs). Results show that oxygen bridges (Co─O─C) formed in the CoTe<sub>2</sub>/Co─O─NC not only effectively shift d-band center of the cobalt near its Fermi level to enhance adsorption of LiPSs but also strengthen the built-in electric fields of CoTe<sub>2</sub>/Co heterojunctions to reduce energy barrier for sulfur conversion. Deposition and dissociation of Li<sub>2</sub>S are significantly enhanced during charging/discharging processes. Durability of highly active catalyst is significantly improved, and rapid cross-interfacial charge transfer is also achieved. The synthesized S/CoTe<sub>2</sub>/Co─O─NC cathode exhibits an initial capacity of 1498 mAh g<sup>−1</sup> at 0.1 C, and its decay rate of capacity over 500 cycles at 0.5 C is only 0.046%. Li─S pouch cells using the cathode show an energy density of 368 Wh kg<sup>−1</sup> and areal capacity of 7.7 mAh cm<sup>−2</sup> at a sulfur loading of 6.7 mg cm<sup>−2</sup>, with an electrolyte/sulfur ratio of 4 µL mg<sup>−1</sup>.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"52 1\",\"pages\":\"\"},\"PeriodicalIF\":18.5000,\"publicationDate\":\"2025-01-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202417834\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202417834","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
锂硫电池被认为是下一代储能系统的候选者,但其缓慢的反应动力学和穿梭效应严重阻碍了其实际应用。其中一个关键的解决方案是设计和应用高效、高稳定和长寿命的催化剂。本文开发了一种纳米结构的CoTe2/Co─O─NC电催化材料,以实现锂多硫化物(LiPSs)的有效吸附和双向催化转化。结果表明,CoTe2/Co─O─NC中形成的氧桥(Co─O─C)不仅有效地将钴在费米能级附近的d带中心移位,增强了对LiPSs的吸附,而且增强了CoTe2/Co异质结的内置电场,降低了硫转化的能垒。在充放电过程中,Li2S的沉积和解离明显增强。显著提高了高活性催化剂的耐久性,并实现了快速的跨界面电荷转移。合成的S/CoTe2/Co─O─NC阴极在0.1 C下的初始容量为1498 mAh g−1,在0.5 C下的500次循环容量衰减率仅为0.046%。在硫负载为6.7 mg cm - 2,电解质/硫比为4 μ L mg - 1的情况下,阴极锂硫袋电池的能量密度为368 Wh kg - 1,面积容量为7.7 mAh cm - 2。
Oxygen Bridges of CoTe2/Co─O─NC Enhancing Adsorption-Catalysis of Polysulfide for Stable Lithium–Sulfur Batteries
Lithium–sulfur batteries are regarded as candidates for next-generation energy storage systems, but their slow reaction kinetics and shuttle effect severely hinder their practical applications. One of the key solutions is to design and apply efficient, highly stable, and long-life catalysts. Herein, a nanostructured CoTe2/Co─O─NC electrocatalytic material is developed to achieve effective adsorption and bidirectional catalytic conversions of lithium polysulfides (LiPSs). Results show that oxygen bridges (Co─O─C) formed in the CoTe2/Co─O─NC not only effectively shift d-band center of the cobalt near its Fermi level to enhance adsorption of LiPSs but also strengthen the built-in electric fields of CoTe2/Co heterojunctions to reduce energy barrier for sulfur conversion. Deposition and dissociation of Li2S are significantly enhanced during charging/discharging processes. Durability of highly active catalyst is significantly improved, and rapid cross-interfacial charge transfer is also achieved. The synthesized S/CoTe2/Co─O─NC cathode exhibits an initial capacity of 1498 mAh g−1 at 0.1 C, and its decay rate of capacity over 500 cycles at 0.5 C is only 0.046%. Li─S pouch cells using the cathode show an energy density of 368 Wh kg−1 and areal capacity of 7.7 mAh cm−2 at a sulfur loading of 6.7 mg cm−2, with an electrolyte/sulfur ratio of 4 µL mg−1.
期刊介绍:
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