阳极
法拉第效率
材料科学
硒化物
异质结
硒化锌
钴
扩散
化学工程
动力学
纳米技术
过渡金属
离子
锂(药物)
电极
光电子学
催化作用
硒
化学
物理化学
冶金
热力学
有机化学
生物化学
量子力学
工程类
物理
内分泌学
医学
作者
Ying Xiao,Yue Miao,Shuang Wan,Yang‐Kook Sun,Shimou Chen
出处
期刊:Small
[Wiley]
日期:2022-06-16
卷期号:18 (28): e2202582-e2202582
被引量:92
标识
DOI:10.1002/smll.202202582
摘要
Abstract The exploitation of effective strategies to accelerate the Na + diffusion kinetics and improve the structural stability in the electrode is extremely important for the development of high efficientcy sodium‐ion batteries. Herein, Se vacancies and heterostructure engineering are utilized to improve the Na + ‐storage performance of transition metal selenides anode prepared through a facile two‐in‐one route. The experimental results coupled with theoretical calculations reveal that the successful construction of the Se vacancies and heterostructure interfaces can effectively lower the Na + diffusion barrier, accelerate the charge transfer efficiency, improve Na + adsorption ability, and provide an abundance of active sites. Consequently, the batteries based on the constructed ZnSe/CoSe 2 ‐CN anode manifest a high initial Coulombic efficiency (97.7%), remarkable specific capacities (547.1 mAh g –1 at 0.5 A g –1 ), superb rate capability (362.1 mAh g –1 at 20 A g –1 ), as well as ultrastable long‐term stability (1000 cycles) with a satisfied specific capacity (535.6 mAh g –1 ) at 1 A g –1 . This work facilitates an in‐depth understanding of the synergistic effect of vacancies and heterojunctions in improving the Na + reaction kinetics, providing an effective strategy to the rational design of key materials for high efficiency rechargeable batteries.
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