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通过葡萄糖辅助合成制备的轨道调制铜掺杂VO纳米花:用于高容量水系铝离子电池的结构优化和电子耦合工程

Orbital-Modulated Cu-Doped VO Nanoflowers via Glucose-Assisted Synthesis: Structural Optimization and Electronic Coupling Engineering for High-Capacity Aqueous Aluminum Ion Batteries.

作者信息

Wang Zhibao, Gu Hanqing, Li Zhanyu

机构信息

Hebei Key Laboratory of Optic-Electronic Information and Materials, National & Local Joint Engineering Laboratory of New Energy Photoelectric Devices, College of Physics Science and Technology, Hebei University, Baoding, 071002, China.

出版信息

Small. 2025 Jul;21(26):e2503861. doi: 10.1002/smll.202503861. Epub 2025 May 5.

Abstract

Vanadium oxide cathode materials in aqueous aluminum-ion batteries (AAIBs) have an exceptional potential for development because of their high valence and fast electron transfer capability. However, the strong electron-electron Coulomb repulsion in vanadium and its associated electrostatic interactions severely hinder the feasibility of vanadium oxides in AAIBs. The glucose-assisted hydrothermal reduction of monoclinic VO combined with Cu ion doping effectively promotes the self-assembly of VO into nanoflower architectures, enabling precise control over morphology and crystalline structure. When integrated with a 5 m Al(OTF) electrolyte and an Ionic liquid (IL )-treated Al sheet anode, this full battery demonstrates outstanding electrochemical performance, achieving an initial discharge capacity of 642 mAh·g at 0.4 A·g. Moreover, introducing Cu orbitals effectively enhances the hybridization and electronic coupling effects between the V and O orbitals. Ex situ characterization and diffusion kinetic provide insights into the embedding/de-embedding mechanism of Al. This work significantly improves the application potential of VO in AAIBs through structural optimization and mechanism studies and provides systematic scientific guidance for the development of vanadium oxide cathode materials.

摘要

水系铝离子电池(AAIBs)中的氧化钒阴极材料因其高价态和快速的电子转移能力而具有巨大的发展潜力。然而,钒中强烈的电子 - 电子库仑排斥及其相关的静电相互作用严重阻碍了氧化钒在水系铝离子电池中的可行性。葡萄糖辅助水热还原单斜VO并结合铜离子掺杂有效地促进了VO自组装成纳米花结构,从而能够精确控制形态和晶体结构。当与5 m Al(OTF)电解质和离子液体(IL)处理的铝板阳极集成时,这种全电池展现出出色的电化学性能,在0.4 A·g下实现了642 mAh·g的初始放电容量。此外,引入铜轨道有效地增强了V和O轨道之间的杂化和电子耦合效应。非原位表征和扩散动力学为铝的嵌入/脱嵌机制提供了深入了解。这项工作通过结构优化和机理研究显著提高了VO在水系铝离子电池中的应用潜力,并为氧化钒阴极材料的开发提供了系统的科学指导。

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