{"title":"超级电容器用V2O5//f-CNT非对称柔性器件的电化学性能","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":"{\"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}","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
摘要
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
Electrochemical Performance of V2O5//f-CNT Asymmetric Flexible Device for Supercapacitor Application
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.
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.