{"title":"Acid etching V2O5 nanowires cathode for high-performance zinc-ion full batteries","authors":"Huan-zhang Wen, Aiqun Kong, Yun-fei Shen, Yun-qi Fan, Jian-jie Liu, Long Chen","doi":"10.1016/j.cej.2025.162148","DOIUrl":null,"url":null,"abstract":"Vanadium oxides are extensively utilized as cathode materials in aqueous zinc-ion batteries (AZIBs) due to the rich redox chemistry of vanadium, while their limited cyclability and sluggish diffusion kinetics impede the practical adoption. Herein, the structural engineering strategy via H<sub>2</sub>SO<sub>4</sub> etching is proposed to modulate the morphology and electronic structure of V<sub>2</sub>O<sub>5</sub> (termed as V<sub>2</sub>O<sub>5</sub>-H<sub>2</sub>SO<sub>4</sub>). Specifically, V<sub>2</sub>O<sub>5</sub> etched H<sub>2</sub>SO<sub>4</sub> features a staggered nanowire architecture and an increased V<sup>5+</sup>/V<sup>4+</sup> ratio, contributing to improving structural stability and accelerating ion transport kinetics. The X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopy reveal that the increased V<sup>5+</sup> diminished Zn<sup>2+</sup> diffusion barriers in V<sub>2</sub>O<sub>5</sub>-H<sub>2</sub>SO<sub>4</sub>, Modified the bonding architecture and furnish extra ion-diffusion channels and ample active sites, thus helping to elucidate the zinc storage mechanism and achieve the excellent electrochemical performance. V<sub>2</sub>O<sub>5</sub>-H<sub>2</sub>SO<sub>4</sub> cathode exhibits an impressive energy output of 391.7 Wh kg<sup>−1</sup> at 152.66 W kg<sup>−1</sup>. The assembled V<sub>2</sub>O<sub>5</sub>-H<sub>2</sub>SO<sub>4</sub>||CuZn<sub>2</sub>/In/InZn<sub>3</sub>@Zn full battery exhibits significantly augmented specific capacity of 588.4 mAh g<sup>−1</sup> at 0.2 A g<sup>−1</sup> and long-cycle stability. This research emphasizes the significance of acid etching on the structural engineering of AZIBs vanadium oxides cathode materials, providing a new approach for structural functional materials.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"183 1","pages":""},"PeriodicalIF":13.3000,"publicationDate":"2025-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.162148","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Vanadium oxides are extensively utilized as cathode materials in aqueous zinc-ion batteries (AZIBs) due to the rich redox chemistry of vanadium, while their limited cyclability and sluggish diffusion kinetics impede the practical adoption. Herein, the structural engineering strategy via H2SO4 etching is proposed to modulate the morphology and electronic structure of V2O5 (termed as V2O5-H2SO4). Specifically, V2O5 etched H2SO4 features a staggered nanowire architecture and an increased V5+/V4+ ratio, contributing to improving structural stability and accelerating ion transport kinetics. The X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopy reveal that the increased V5+ diminished Zn2+ diffusion barriers in V2O5-H2SO4, Modified the bonding architecture and furnish extra ion-diffusion channels and ample active sites, thus helping to elucidate the zinc storage mechanism and achieve the excellent electrochemical performance. V2O5-H2SO4 cathode exhibits an impressive energy output of 391.7 Wh kg−1 at 152.66 W kg−1. The assembled V2O5-H2SO4||CuZn2/In/InZn3@Zn full battery exhibits significantly augmented specific capacity of 588.4 mAh g−1 at 0.2 A g−1 and long-cycle stability. This research emphasizes the significance of acid etching on the structural engineering of AZIBs vanadium oxides cathode materials, providing a new approach for structural functional materials.
钒氧化物由于其丰富的氧化还原化学性质而被广泛用作水性锌离子电池(AZIBs)的正极材料,但其有限的循环性能和缓慢的扩散动力学阻碍了其实际应用。本文提出了通过H2SO4蚀刻的结构工程策略来调节V2O5(称为V2O5-H2SO4)的形态和电子结构。具体来说,V2O5蚀刻H2SO4具有交错的纳米线结构和更高的V5+/V4+比率,有助于提高结构稳定性和加速离子传输动力学。x射线吸收近边结构(XANES)和扩展x射线吸收精细结构(EXAFS)谱分析结果表明,V5 - h2so4中V5+的增加减少了Zn2+的扩散势垒,改变了键结构,提供了额外的离子扩散通道和充足的活性位点,从而有助于阐明锌的储存机理,实现了优异的电化学性能。在152.66 W kg−1时,V2O5-H2SO4阴极显示出令人印象深刻的能量输出为391.7 Wh kg−1。组装后的V2O5-H2SO4||CuZn2/In/InZn3@Zn全电池在0.2 A g- 1下的比容量达到588.4 mAh g- 1,且具有长周期稳定性。本研究强调了酸蚀在azib钒氧化物正极材料结构工程中的重要意义,为结构功能材料提供了新的途径。
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.