Yuan Xie, Jia Wen, Junyuan Huang, Rong Jiang, Longjun Dai, Yang Ren, Zhu Liu and Xiaowei Zhou
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Compared to the original VO<small><sub><em>x</em></sub></small>-NT, K-VO<small><sub><em>x</em></sub></small>-NT exhibited significantly enhanced cycling stability and rate performance when serving as the cathode in potassium-ion batteries (PIBs). It demonstrated a reversible discharge specific capacity of 75.7 mA h g<small><sup>−1</sup></small> for the 1st cycle at a current density of 50 mA g<small><sup>−1</sup></small> within a voltage range of 1.5–3.8 V (<em>vs.</em> K<small><sup>+</sup></small>/K) and retained 62.2 mA h g<small><sup>−1</sup></small> after the 50th cycle. When a current density of 600 mA g<small><sup>−1</sup></small> was applied, it could still deliver a capacity of 44.3 mA h g<small><sup>−1</sup></small>. Furthermore, the storage and degradation mechanisms of K<small><sup>+</sup></small> in K-VO<small><sub><em>x</em></sub></small>-NT were elucidated. In addition, using hard carbon as the anode, the K-VO<small><sub><em>x</em></sub></small>-NT full-cell was tested to further evaluate its practical performance. This work provides insight into the design and modification of vanadium-based cathode materials for future PIBs.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 5","pages":" 3339-3352"},"PeriodicalIF":4.6000,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d4ra07672a?page=search","citationCount":"0","resultStr":"{\"title\":\"Preparation and structural optimization of vanadium oxide nanotubes as cathode materials for PIBs with improved performance†\",\"authors\":\"Yuan Xie, Jia Wen, Junyuan Huang, Rong Jiang, Longjun Dai, Yang Ren, Zhu Liu and Xiaowei Zhou\",\"doi\":\"10.1039/D4RA07672A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In this work, we synthesized hollow multi-walled vanadium oxide nanotubes (VO<small><sub><em>x</em></sub></small>-NT) using a soft template technique under hydrothermal reaction conditions. 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引用次数: 0
摘要
本文在水热反应条件下,采用软模板技术合成了空心多壁氧化钒纳米管(VOx-NT)。通过在溶液环境中用K+取代不促进电化学钾储存的有机模板,我们在获得K-VOx-NT材料的同时有效地保留了VOx-NT原有的中空多壁结构。我们对这些材料的微观结构、形态和组成进行了系统的表征,并评估了它们的钾储存性能。与原VOx-NT相比,K-VOx-NT在钾离子电池(PIBs)中作为阴极时表现出明显增强的循环稳定性和倍率性能。在1.5 ~ 3.8 V (vs. K+/K)电压范围内,电流密度为50 mA g−1时,第一次循环的可逆放电比容量为75.7 mA h g−1,第50次循环后保持62.2 mA h g−1。当施加600 mA g−1的电流密度时,它仍然可以提供44.3 mA h g−1的容量。进一步阐明了K+在K- vox - nt中的储存和降解机制。此外,以硬碳为阳极,对K-VOx-NT全电池进行了测试,进一步评价了其实际性能。这项工作为未来PIBs的钒基阴极材料的设计和改进提供了见解。
Preparation and structural optimization of vanadium oxide nanotubes as cathode materials for PIBs with improved performance†
In this work, we synthesized hollow multi-walled vanadium oxide nanotubes (VOx-NT) using a soft template technique under hydrothermal reaction conditions. By replacing organic templates, which do not contribute to electrochemical potassium storage, with K+ in a solution environment, we effectively retained the original hollow multi-walled structure of VOx-NT while obtaining the K-VOx-NT material. We conducted systematic characterizations of the microstructure, morphology, and composition of these materials and evaluated their potassium storage performance. Compared to the original VOx-NT, K-VOx-NT exhibited significantly enhanced cycling stability and rate performance when serving as the cathode in potassium-ion batteries (PIBs). It demonstrated a reversible discharge specific capacity of 75.7 mA h g−1 for the 1st cycle at a current density of 50 mA g−1 within a voltage range of 1.5–3.8 V (vs. K+/K) and retained 62.2 mA h g−1 after the 50th cycle. When a current density of 600 mA g−1 was applied, it could still deliver a capacity of 44.3 mA h g−1. Furthermore, the storage and degradation mechanisms of K+ in K-VOx-NT were elucidated. In addition, using hard carbon as the anode, the K-VOx-NT full-cell was tested to further evaluate its practical performance. This work provides insight into the design and modification of vanadium-based cathode materials for future PIBs.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.