材料科学
阳极
离子
空位缺陷
电极
纳米技术
化学物理
光电子学
分析化学(期刊)
凝聚态物理
物理化学
化学
物理
量子力学
色谱法
作者
Enzhi Li,Mingshan Wang,Wen Xu,Daniel Höche,Yuanlong Feng,Junchen Chen,Bo Yu,Bingshu Guo,Zhiyuan Ma,Yun Huang,Xing Li,Guozhong Cao
标识
DOI:10.1002/aenm.202405674
摘要
Abstract Optimizing electrochemical kinetics by regulation ion/charge transfer efficiency and stabilizing the electrode structure of electrode materials is crucial to maximize the rapid charging and long cycling sodium‐ion storage. Herein, VS 2 /Bi 2 S 3 spring‐type heterointerfaces hollow microspheres with spatial confinement and sulfur vacancy defects are synthesized as a fast‐charging anode for sodium‐ion hybrid capacitors (SIHCs). The experimental studies coupled with density functional theory calculations verify that the strong coupling between VS 2 and Bi 2 S 3 induces a stable built‐in electric field, largely promoting the charge and sodium‐ion transfer efficiency. Sulfur vacancy defects at the heterointerfaces produce additional sodium‐ion pseudocapacitive storage, which improves the reversible capacity and large‐rate fast charge performance of the VS 2 /Bi 2 S 3 electrode. Finite element analysis and in situ expansion test confirm that the spring‐type heterostructured hollow microspheres formed by flat‐morphology VS 2 and zigzag‐morphology Bi 2 S 3 stacking mitigate the lattice expansion and contraction during sodium‐ion insertion/extraction, accommodate the mechanical stresses, and maintain the integrity of the heterojunction interface. When employed in coin SIHC, it achieves a high energy/power density of 135 Wh kg −1 /22 kW kg −1 , and an ultralong life of 50 000 cycles; the assembled pouch SIHC (1 Ah) demonstrates a high specific energy of 120 Wh kg −1 with fast‐charging at 10 C, and 95.5% capacity retention after 1000 cycles.
科研通智能强力驱动
Strongly Powered by AbleSci AI