{"title":"Electrochemical Performance of V2O5//f-CNT Asymmetric Flexible Device for Supercapacitor Application","authors":"Mamta Bulla, Vinay Kumar, Raman Devi, Sunil Kumar, Sarita Sindhu, Rita Dahiya, Anushree Jatrana, Ajay Kumar Mishra, Raj Bahadur Singh","doi":"10.1007/s10904-025-03647-1","DOIUrl":null,"url":null,"abstract":"<div><p>The advancement of flexible supercapacitors has been constrained by the inherent difficulty of fabricating flexible electrodes. In this work, the V<sub>2</sub>O<sub>5</sub> nanostructures were synthesized at different temperatures (120–200 °C) via hydrothermal treatment, followed by calcination, resulting in materials with high porosity and optimized electrochemical properties. The fabricated electrode (synthesized V<sub>2</sub>O<sub>5</sub> at 180 °C) shows a maximum capacitance (178.5 F g⁻<sup>1</sup> at 1 A g⁻<sup>1</sup> current density) compared to other prepared samples 1 in a 1.0 M Na<sub>2</sub>SO<sub>4</sub> aqueous electrolyte. For practical applications, V<sub>2</sub>O<sub>5</sub> nanostructures were integrated with f-CNTs to fabricate the V<sub>2</sub>O<sub>5</sub>//f-CNT asymmetric supercapacitor device, achieving a specific capacitance of 104.4 F g⁻<sup>1</sup> at 1 A g⁻<sup>1</sup> within a 1.6 V voltage window, signifying improved charge storage capabilities. The device achieved an energy density of 37.12 Wh kg⁻<sup>1</sup> and a power density of 800 W kg⁻<sup>1</sup> at 1 A g⁻<sup>1</sup>. The synergistic integration of Faradaic reactions from V₂O₅ with the EDL capacitance of f-CNTs enabled the device to retain 91.2% of its capacitance after 2000 GCD cycles, with enhanced performance sustained up to 5000 cycles. Furthermore, the device demonstrated remarkable flexibility, losing only 4.3% of its capacitance when bent at a 90° angle, underscoring its potential as a high-performance energy storage solution.</p><h3>Graphical Abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":639,"journal":{"name":"Journal of Inorganic and Organometallic Polymers and Materials","volume":"35 8","pages":"6176 - 6190"},"PeriodicalIF":4.9000,"publicationDate":"2025-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inorganic and Organometallic Polymers and Materials","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10904-025-03647-1","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The advancement of flexible supercapacitors has been constrained by the inherent difficulty of fabricating flexible electrodes. In this work, the V2O5 nanostructures were synthesized at different temperatures (120–200 °C) via hydrothermal treatment, followed by calcination, resulting in materials with high porosity and optimized electrochemical properties. The fabricated electrode (synthesized V2O5 at 180 °C) shows a maximum capacitance (178.5 F g⁻1 at 1 A g⁻1 current density) compared to other prepared samples 1 in a 1.0 M Na2SO4 aqueous electrolyte. For practical applications, V2O5 nanostructures were integrated with f-CNTs to fabricate the V2O5//f-CNT asymmetric supercapacitor device, achieving a specific capacitance of 104.4 F g⁻1 at 1 A g⁻1 within a 1.6 V voltage window, signifying improved charge storage capabilities. The device achieved an energy density of 37.12 Wh kg⁻1 and a power density of 800 W kg⁻1 at 1 A g⁻1. The synergistic integration of Faradaic reactions from V₂O₅ with the EDL capacitance of f-CNTs enabled the device to retain 91.2% of its capacitance after 2000 GCD cycles, with enhanced performance sustained up to 5000 cycles. Furthermore, the device demonstrated remarkable flexibility, losing only 4.3% of its capacitance when bent at a 90° angle, underscoring its potential as a high-performance energy storage solution.
柔性超级电容器的发展一直受到制造柔性电极的固有困难的制约。在不同温度(120 ~ 200℃)下,通过水热处理和煅烧合成了V2O5纳米结构,得到了高孔隙率和优化的电化学性能的材料。与其他制备的样品相比,在1.0 M Na2SO4水溶液中制备的电极(在180°C下合成V2O5)显示出最大的电容(在1 a g⁻1电流密度下为178.5 F g⁻1)。在实际应用中,V2O5纳米结构与F - cnt相结合,制造了V2O5// F - cnt不对称超级电容器器件,在1.6 V电压窗口内,在1 ag⁻1下实现了104.4 F g⁻1的比电容,这表明电荷存储能力得到了提高。该装置的能量密度为37.12 Wh kg - 1,在1 a g - 1时的功率密度为800 W kg - 1。V₂O₅的法拉第反应与f-CNTs的EDL电容的协同集成使该器件在2000个GCD循环后保持其电容的91.2%,性能持续提高至5000个循环。此外,该器件表现出了卓越的灵活性,在弯曲90°时仅损失4.3%的电容,强调了其作为高性能储能解决方案的潜力。图形抽象
期刊介绍:
Journal of Inorganic and Organometallic Polymers and Materials [JIOP or JIOPM] is a comprehensive resource for reports on the latest theoretical and experimental research. This bimonthly journal encompasses a broad range of synthetic and natural substances which contain main group, transition, and inner transition elements. The publication includes fully peer-reviewed original papers and shorter communications, as well as topical review papers that address the synthesis, characterization, evaluation, and phenomena of inorganic and organometallic polymers, materials, and supramolecular systems.