{"title":"层叠CoS1.097/V3S4异质结纳米片的构建对钠离子电池反应动力学和循环稳定性的增强","authors":"Jiahui Ma, Fangshun Zhu, Wenwen Li, Quangui Ma, Rajaiah Alexpandi, Yurong Cai, Jiayuan Xiang, Fangfang Tu","doi":"10.1016/j.jallcom.2024.178290","DOIUrl":null,"url":null,"abstract":"In recent years, sodium-ion batteries (SIBs) have gained significant attention as a viable alternative to lithium-ion batteries due to the abundance of sodium, its low cost, and its similar electrochemical behavior compared to lithium. A key approach to enhancing SIB anode performance is designing stable electrode structures that minimize sodium ion-diffusion pathways. In this study, we synthesized a sheet-like stacked CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> heterostructure via a hydrothermal method. The CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> composite combines the high specific capacity of CoS<sub>1.097</sub> with the excellent cycling stability of V<sub>3</sub>S<sub>4</sub>. Notably, the heterojunction generates an integrated electric field that reduces activation energy, accelerates charge transfer, and enhances reaction kinetics. The CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> heterostructure exhibits an initial discharge capacity of 833.8 mAh g⁻¹ at 0.5<!-- --> <!-- -->A<!-- --> <!-- -->g⁻¹ and a reversible capacity of 505.8 mAh g⁻¹ after 100 cycles. Impressively, even at a high current density of 5<!-- --> <!-- -->A<!-- --> <!-- -->g⁻¹, the electrode retains a capacity of 330.8 mAh g⁻¹ after 1000 cycles. This study demonstrates a promising approach for developing SIB anode materials with superior performance, high reversibility, and long-term cycling durability, supported by the synergistic effect of the CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> heterojunction.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"25 1","pages":""},"PeriodicalIF":6.3000,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Construction of stacked CoS1.097/V3S4 heterojunction nanosheets towards the enhanced reaction kinetics and cycling stability of sodium-ion batteries\",\"authors\":\"Jiahui Ma, Fangshun Zhu, Wenwen Li, Quangui Ma, Rajaiah Alexpandi, Yurong Cai, Jiayuan Xiang, Fangfang Tu\",\"doi\":\"10.1016/j.jallcom.2024.178290\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In recent years, sodium-ion batteries (SIBs) have gained significant attention as a viable alternative to lithium-ion batteries due to the abundance of sodium, its low cost, and its similar electrochemical behavior compared to lithium. A key approach to enhancing SIB anode performance is designing stable electrode structures that minimize sodium ion-diffusion pathways. In this study, we synthesized a sheet-like stacked CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> heterostructure via a hydrothermal method. The CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> composite combines the high specific capacity of CoS<sub>1.097</sub> with the excellent cycling stability of V<sub>3</sub>S<sub>4</sub>. Notably, the heterojunction generates an integrated electric field that reduces activation energy, accelerates charge transfer, and enhances reaction kinetics. The CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> heterostructure exhibits an initial discharge capacity of 833.8 mAh g⁻¹ at 0.5<!-- --> <!-- -->A<!-- --> <!-- -->g⁻¹ and a reversible capacity of 505.8 mAh g⁻¹ after 100 cycles. Impressively, even at a high current density of 5<!-- --> <!-- -->A<!-- --> <!-- -->g⁻¹, the electrode retains a capacity of 330.8 mAh g⁻¹ after 1000 cycles. This study demonstrates a promising approach for developing SIB anode materials with superior performance, high reversibility, and long-term cycling durability, supported by the synergistic effect of the CoS<sub>1.097</sub>/V<sub>3</sub>S<sub>4</sub> heterojunction.\",\"PeriodicalId\":344,\"journal\":{\"name\":\"Journal of Alloys and Compounds\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2024-12-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Alloys and Compounds\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jallcom.2024.178290\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jallcom.2024.178290","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
近年来,钠离子电池(SIBs)作为锂离子电池的可行替代品受到了极大的关注,因为钠含量丰富,成本低,并且与锂相比具有相似的电化学行为。提高SIB阳极性能的关键方法是设计稳定的电极结构,使钠离子扩散途径最小化。在本研究中,我们通过水热法合成了片状堆叠的CoS1.097/V3S4异质结构。CoS1.097/V3S4复合材料结合了CoS1.097的高比容量和V3S4的优良循环稳定性。值得注意的是,异质结产生了一个集成电场,降低了活化能,加速了电荷转移,提高了反应动力学。CoS1.097/V3S4异质结构在0.5 A g⁻¹时的初始放电容量为833.8 mAh g⁻¹,100次循环后的可逆容量为505.8 mAh g⁻¹。令人印象深刻的是,即使在5毫克(⁻¹)的高电流密度下,电极在1000次循环后仍保持330.8毫安(⁻¹)的容量。在CoS1.097/V3S4异质结的协同作用下,本研究展示了一种具有优异性能、高可逆性和长期循环耐久性的SIB阳极材料的开发方法。
Construction of stacked CoS1.097/V3S4 heterojunction nanosheets towards the enhanced reaction kinetics and cycling stability of sodium-ion batteries
In recent years, sodium-ion batteries (SIBs) have gained significant attention as a viable alternative to lithium-ion batteries due to the abundance of sodium, its low cost, and its similar electrochemical behavior compared to lithium. A key approach to enhancing SIB anode performance is designing stable electrode structures that minimize sodium ion-diffusion pathways. In this study, we synthesized a sheet-like stacked CoS1.097/V3S4 heterostructure via a hydrothermal method. The CoS1.097/V3S4 composite combines the high specific capacity of CoS1.097 with the excellent cycling stability of V3S4. Notably, the heterojunction generates an integrated electric field that reduces activation energy, accelerates charge transfer, and enhances reaction kinetics. The CoS1.097/V3S4 heterostructure exhibits an initial discharge capacity of 833.8 mAh g⁻¹ at 0.5 A g⁻¹ and a reversible capacity of 505.8 mAh g⁻¹ after 100 cycles. Impressively, even at a high current density of 5 A g⁻¹, the electrode retains a capacity of 330.8 mAh g⁻¹ after 1000 cycles. This study demonstrates a promising approach for developing SIB anode materials with superior performance, high reversibility, and long-term cycling durability, supported by the synergistic effect of the CoS1.097/V3S4 heterojunction.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.