{"title":"A flower-like VO2(B)/V2CTx heterojunction as high kinetic rechargeable anode for sodium-ion batteries","authors":"Xiaoyu Jin, Yongxin Huang, Mengmeng Zhang, Ziheng Wang, Qianqian Meng, Zhihang Song, Li Li, Feng Wu, Renjie Chen","doi":"10.1002/bte2.20230029","DOIUrl":null,"url":null,"abstract":"<p>VO<sub>2</sub>(B) is considered as a promising anode material for the next-generation sodium-ion batteries (SIBs) due to its accessible raw materials and considerable theoretical capacity. However, the VO<sub>2</sub>(B) electrode has inherent defects such as low conductivity and serious volume expansion, which hinder their practical application. Herein, a flower-like VO<sub>2</sub>(B)/V<sub>2</sub>CT<sub>x</sub> (VO@VC) heterojunction was prepared by a simple hydrothermal synthesis method with in situ growth. The flower-like structure composed of thin nanosheets alleviates the volume expansion, as well as the rapid Na<sup>+</sup> transport pathways are built by the heterojunction structure, resulting in long-term cycling stability and superior rate performance. At a current density of 100 mA g<sup>−1</sup>, VO@VC anode can maintain a specific capacity of 276 mAh g<sup>−1</sup> with an average coulombic efficiency of 98.7% after 100 cycles. Additionally, even at a current density of 2 A g<sup>−1</sup>, the VO@VC anode still exhibited a capacity of 132.9 mAh g<sup>−1</sup> for 1000 cycles. The enhanced reaction kinetics can be attributed to the fast Na<sup>+</sup> adsorption and storage at interfaces, which has been confirmed by the experimental and theoretical methods. These results demonstrate that the tailored nanoarchitecture design and additional surface engineering are effective strategies for optimizing vanadium-based anode.</p>","PeriodicalId":8807,"journal":{"name":"Battery Energy","volume":"2 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bte2.20230029","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Battery Energy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bte2.20230029","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
VO2(B) is considered as a promising anode material for the next-generation sodium-ion batteries (SIBs) due to its accessible raw materials and considerable theoretical capacity. However, the VO2(B) electrode has inherent defects such as low conductivity and serious volume expansion, which hinder their practical application. Herein, a flower-like VO2(B)/V2CTx (VO@VC) heterojunction was prepared by a simple hydrothermal synthesis method with in situ growth. The flower-like structure composed of thin nanosheets alleviates the volume expansion, as well as the rapid Na+ transport pathways are built by the heterojunction structure, resulting in long-term cycling stability and superior rate performance. At a current density of 100 mA g−1, VO@VC anode can maintain a specific capacity of 276 mAh g−1 with an average coulombic efficiency of 98.7% after 100 cycles. Additionally, even at a current density of 2 A g−1, the VO@VC anode still exhibited a capacity of 132.9 mAh g−1 for 1000 cycles. The enhanced reaction kinetics can be attributed to the fast Na+ adsorption and storage at interfaces, which has been confirmed by the experimental and theoretical methods. These results demonstrate that the tailored nanoarchitecture design and additional surface engineering are effective strategies for optimizing vanadium-based anode.
摘要VO 2 (B)由于其易于获取的原料和可观的理论容量,被认为是下一代钠离子电池(sib)极有前途的负极材料。然而,VO 2 (B)电极存在电导率低、体积膨胀严重等固有缺陷,阻碍了其实际应用。本文采用原位生长的简单水热合成方法制备了花状的vo2 (B)/ v2ct x (VO@VC)异质结。由纳米薄片组成的花状结构减轻了体积膨胀,并且异质结结构建立了快速的Na +运输途径,从而实现了长期循环稳定性和优越的速率性能。当电流密度为100 mA g−1时,VO@VC阳极在100次循环后可保持276 mAh g−1的比容量,平均库仑效率为98.7%。此外,即使在2 a g−1的电流密度下,VO@VC阳极在1000次循环中仍然显示出132.9 mAh g−1的容量。反应动力学的增强可归因于Na +在界面上的快速吸附和储存,这已被实验和理论方法所证实。这些结果表明,定制纳米结构设计和额外的表面工程是优化钒基阳极的有效策略。