{"title":"ZIF-67纳米立方组装衍生的CoTe2纳米颗粒封装分层碳纳米纤维实现高效锂存储。","authors":"Wu-Di Zhang, Xiao-Ye Ge, Kang-Kang Zhao, Qiang Zhang, Fu-Hu Cao, Xingyu Guo, Chuan-Ling Zhang","doi":"10.1016/j.jcis.2024.12.040","DOIUrl":null,"url":null,"abstract":"<p><p>Tellurides are promising anode materials for lithium-ion batteries (LIBs) because of their high electronic conductivity and energy density. However, the slow kinetics and poor structural stability lead to decreased electrochemical performance. In this work, by utilizing the interface magnetization mechanism and assembly effect, high-performance CoTe<sub>2</sub> nanoparticles encapsulated hierarchical N-doped porous carbon nanofibers were rationally designed and prepared (ES-CoTe<sub>2</sub>@NC) via facile tellurization of one-dimensional (1D) ZIF-67 nanocube assemblies. Benefiting from the synergistic effects of the unique structure and component, the ES-CoTe<sub>2</sub>@NC anode exhibits a high reversible capacity of 1020 mAh/g at 0.1 A/g after 200 cycles, along with excellent long-term cycling stability, retaining a capacity of 780 mAh/g at 1 A g<sup>-1</sup> after 500 cycles. Notably, the ES-CoTe<sub>2</sub>@NC anode retains a remarkable capacity of 502 mAh/g even after 1000 cycles at a high current density of 5 A g<sup>-1</sup>, highlighting its exceptional cycling stability. Besides, the Full cell coupled with LiFePO<sub>4</sub> cathode delivers a high reversible capacity of 151.1 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup> with stable cycling performance. The kinetics analysis reveals that the ES-CoTe<sub>2</sub>@NC anode has high pseudocapacitive properties, high electronic conductivity, and fast Li<sup>+</sup> diffusion capability. Moreover, the ex-situ characterization clarifies the conversion reaction mechanism of ES-CoTe<sub>2</sub>@NC. This work provides a facile but effective way to construct high-performance CoTe<sub>2</sub>-based electrodes.</p>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"682 ","pages":"1028-1039"},"PeriodicalIF":9.4000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"ZIF-67 nanocubes assembly-derived CoTe<sub>2</sub> nanoparticles encapsulated hierarchical carbon nanofibers enables efficient lithium storage.\",\"authors\":\"Wu-Di Zhang, Xiao-Ye Ge, Kang-Kang Zhao, Qiang Zhang, Fu-Hu Cao, Xingyu Guo, Chuan-Ling Zhang\",\"doi\":\"10.1016/j.jcis.2024.12.040\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Tellurides are promising anode materials for lithium-ion batteries (LIBs) because of their high electronic conductivity and energy density. However, the slow kinetics and poor structural stability lead to decreased electrochemical performance. In this work, by utilizing the interface magnetization mechanism and assembly effect, high-performance CoTe<sub>2</sub> nanoparticles encapsulated hierarchical N-doped porous carbon nanofibers were rationally designed and prepared (ES-CoTe<sub>2</sub>@NC) via facile tellurization of one-dimensional (1D) ZIF-67 nanocube assemblies. Benefiting from the synergistic effects of the unique structure and component, the ES-CoTe<sub>2</sub>@NC anode exhibits a high reversible capacity of 1020 mAh/g at 0.1 A/g after 200 cycles, along with excellent long-term cycling stability, retaining a capacity of 780 mAh/g at 1 A g<sup>-1</sup> after 500 cycles. Notably, the ES-CoTe<sub>2</sub>@NC anode retains a remarkable capacity of 502 mAh/g even after 1000 cycles at a high current density of 5 A g<sup>-1</sup>, highlighting its exceptional cycling stability. Besides, the Full cell coupled with LiFePO<sub>4</sub> cathode delivers a high reversible capacity of 151.1 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup> with stable cycling performance. The kinetics analysis reveals that the ES-CoTe<sub>2</sub>@NC anode has high pseudocapacitive properties, high electronic conductivity, and fast Li<sup>+</sup> diffusion capability. Moreover, the ex-situ characterization clarifies the conversion reaction mechanism of ES-CoTe<sub>2</sub>@NC. This work provides a facile but effective way to construct high-performance CoTe<sub>2</sub>-based electrodes.</p>\",\"PeriodicalId\":351,\"journal\":{\"name\":\"Journal of Colloid and Interface Science\",\"volume\":\"682 \",\"pages\":\"1028-1039\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2025-03-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Colloid and Interface Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jcis.2024.12.040\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Colloid and Interface Science","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.jcis.2024.12.040","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
碲化物具有较高的电导率和能量密度,是锂离子电池极具发展前景的负极材料。然而,由于反应速度慢,结构稳定性差,导致其电化学性能下降。本研究利用界面磁化机制和组装效应,通过对一维(1D) ZIF-67纳米立方体组件的易碲化,合理设计并制备了高性能的CoTe2纳米颗粒封装分层掺n多孔碳纳米纤维(ES-CoTe2@NC)。得益于独特的结构和组件的协同效应,ES-CoTe2@NC阳极在200次循环后,在0.1 a /g下具有1020 mAh/g的高可逆容量,同时具有优异的长期循环稳定性,在500次循环后,在1 a g-1下保持780 mAh/g的容量。值得注意的是,ES-CoTe2@NC阳极在5 a g-1的高电流密度下,即使在1000次循环后仍保持502 mAh/g的显着容量,突出了其出色的循环稳定性。此外,与LiFePO4阴极耦合的Full电池在0.1 a g-1下具有151.1 mAh g-1的高可逆容量,且循环性能稳定。动力学分析表明,ES-CoTe2@NC阳极具有高赝电容性、高电子导电性和快速Li+扩散能力。此外,外原位表征澄清了ES-CoTe2@NC的转化反应机理。这项工作为构建高性能cote2基电极提供了一种简单而有效的方法。
Tellurides are promising anode materials for lithium-ion batteries (LIBs) because of their high electronic conductivity and energy density. However, the slow kinetics and poor structural stability lead to decreased electrochemical performance. In this work, by utilizing the interface magnetization mechanism and assembly effect, high-performance CoTe2 nanoparticles encapsulated hierarchical N-doped porous carbon nanofibers were rationally designed and prepared (ES-CoTe2@NC) via facile tellurization of one-dimensional (1D) ZIF-67 nanocube assemblies. Benefiting from the synergistic effects of the unique structure and component, the ES-CoTe2@NC anode exhibits a high reversible capacity of 1020 mAh/g at 0.1 A/g after 200 cycles, along with excellent long-term cycling stability, retaining a capacity of 780 mAh/g at 1 A g-1 after 500 cycles. Notably, the ES-CoTe2@NC anode retains a remarkable capacity of 502 mAh/g even after 1000 cycles at a high current density of 5 A g-1, highlighting its exceptional cycling stability. Besides, the Full cell coupled with LiFePO4 cathode delivers a high reversible capacity of 151.1 mAh g-1 at 0.1 A g-1 with stable cycling performance. The kinetics analysis reveals that the ES-CoTe2@NC anode has high pseudocapacitive properties, high electronic conductivity, and fast Li+ diffusion capability. Moreover, the ex-situ characterization clarifies the conversion reaction mechanism of ES-CoTe2@NC. This work provides a facile but effective way to construct high-performance CoTe2-based electrodes.
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies