{"title":"多维封装几何加速的硒化铋阳极材料与快速动力学优越的钾离子储存","authors":"Zhenzhen Wang, Shuangyan Qiao, Yanshu Zhao, Lingling Yuan, Ting Li, Shaokun Chong","doi":"10.1016/j.jallcom.2025.180329","DOIUrl":null,"url":null,"abstract":"Conversion-alloying anode materials exhibit ultra-high theoretical specific capacity for potassium-ion batteries (PIBs) based on multi-electron transfer reaction. However, large volume variation and sluggish electrochemical kinetics have become key issues limiting its cyclability and rate capability. Herein, Bi<sub>2</sub>Se<sub>3</sub> micro-flowers intertwined with one-dimensional carbon nanotube, anchored on two-dimensional reduced graphene oxide and encapsulated by three-dimensional N-doped C (Bi<sub>2</sub>Se<sub>3</sub>@rGO@NC/CNT) are constructed as anode materials for PIBs. The multidimensional hierarchical confinement effect boosts Bi<sub>2</sub>Se<sub>3</sub> to exhibit fast electron/K-ion transport kinetics and great K-ion adsorption ability, as well as superior structure stability with the reduced lattice stress, where the stable existence of C-Se bond and Bi-O-C bonds plays an important role in maintaining interfacial stability of composite. It is illustrated that K-ion insertion into and extraction from Bi<sub>2</sub>Se<sub>3</sub> via conversion-alloying dual-mechanism using Bi as the redox center based on 12-electron transfer per formular. Therefore, Bi<sub>2</sub>Se<sub>3</sub>@rGO@NC/CNT architecture contributes high initial specific capacity, excellent rate capability and cycling stability with ultra-long lifetime over 1000 cycles and low-capacity decay rate of 0.068% per cycle. This work lays a theoretical and experimental basis for the construction of high-performance conversion-alloying anode for PIBs.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"30 9 1","pages":""},"PeriodicalIF":6.3000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multidimensional encapsulation geometry boosting bismuth selenide anode material with fast kinetics for superior potassium-ion storage\",\"authors\":\"Zhenzhen Wang, Shuangyan Qiao, Yanshu Zhao, Lingling Yuan, Ting Li, Shaokun Chong\",\"doi\":\"10.1016/j.jallcom.2025.180329\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Conversion-alloying anode materials exhibit ultra-high theoretical specific capacity for potassium-ion batteries (PIBs) based on multi-electron transfer reaction. However, large volume variation and sluggish electrochemical kinetics have become key issues limiting its cyclability and rate capability. Herein, Bi<sub>2</sub>Se<sub>3</sub> micro-flowers intertwined with one-dimensional carbon nanotube, anchored on two-dimensional reduced graphene oxide and encapsulated by three-dimensional N-doped C (Bi<sub>2</sub>Se<sub>3</sub>@rGO@NC/CNT) are constructed as anode materials for PIBs. The multidimensional hierarchical confinement effect boosts Bi<sub>2</sub>Se<sub>3</sub> to exhibit fast electron/K-ion transport kinetics and great K-ion adsorption ability, as well as superior structure stability with the reduced lattice stress, where the stable existence of C-Se bond and Bi-O-C bonds plays an important role in maintaining interfacial stability of composite. It is illustrated that K-ion insertion into and extraction from Bi<sub>2</sub>Se<sub>3</sub> via conversion-alloying dual-mechanism using Bi as the redox center based on 12-electron transfer per formular. Therefore, Bi<sub>2</sub>Se<sub>3</sub>@rGO@NC/CNT architecture contributes high initial specific capacity, excellent rate capability and cycling stability with ultra-long lifetime over 1000 cycles and low-capacity decay rate of 0.068% per cycle. 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引用次数: 0
摘要
基于多电子转移反应,转化合金阳极材料在钾离子电池(PIB)中表现出超高的理论比容量。然而,较大的体积变化和缓慢的电化学动力学已成为限制其循环性和速率能力的关键问题。在此,我们构建了与一维碳纳米管交织、锚定在二维还原氧化石墨烯上并被三维掺杂 N 的 C 包覆的 Bi2Se3 微流(Bi2Se3@rGO@NC/CNT),作为 PIB 的阳极材料。多维分层束缚效应使 Bi2Se3 表现出快速的电子/K 离子传输动力学和强大的 K 离子吸附能力,并随着晶格应力的降低而具有优异的结构稳定性,其中 C-Se 键和 Bi-O-C 键的稳定存在对维持复合材料的界面稳定性起着重要作用。研究表明,以 Bi 为氧化还原中心,通过转换-合金化双重机制,K 离子可插入 Bi2Se3 并从 Bi2Se3 中萃取出来。因此,Bi2Se3@rGO@NC/CNT 结构具有较高的初始比容量、出色的速率能力和循环稳定性,可实现 1000 次以上的超长寿命和每循环 0.068% 的低容量衰减率。这项工作为构建高性能 PIB 转换合金阳极奠定了理论和实验基础。
Multidimensional encapsulation geometry boosting bismuth selenide anode material with fast kinetics for superior potassium-ion storage
Conversion-alloying anode materials exhibit ultra-high theoretical specific capacity for potassium-ion batteries (PIBs) based on multi-electron transfer reaction. However, large volume variation and sluggish electrochemical kinetics have become key issues limiting its cyclability and rate capability. Herein, Bi2Se3 micro-flowers intertwined with one-dimensional carbon nanotube, anchored on two-dimensional reduced graphene oxide and encapsulated by three-dimensional N-doped C (Bi2Se3@rGO@NC/CNT) are constructed as anode materials for PIBs. The multidimensional hierarchical confinement effect boosts Bi2Se3 to exhibit fast electron/K-ion transport kinetics and great K-ion adsorption ability, as well as superior structure stability with the reduced lattice stress, where the stable existence of C-Se bond and Bi-O-C bonds plays an important role in maintaining interfacial stability of composite. It is illustrated that K-ion insertion into and extraction from Bi2Se3 via conversion-alloying dual-mechanism using Bi as the redox center based on 12-electron transfer per formular. Therefore, Bi2Se3@rGO@NC/CNT architecture contributes high initial specific capacity, excellent rate capability and cycling stability with ultra-long lifetime over 1000 cycles and low-capacity decay rate of 0.068% per cycle. This work lays a theoretical and experimental basis for the construction of high-performance conversion-alloying anode for PIBs.
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.