Timofey Averianov, Kyle Matthews, Xinle Zhang, Huyen T. K. Nguyen, Yuan Zhang, Yury Gogotsi and Ekaterina Pomerantseva*,
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引用次数: 0
Abstract
Layered hydrated vanadium oxides, particularly those with bilayered structures, show remarkable electrochemical performance as cathodes for aqueous Zn-ion batteries (AZIBs). However, their wide-scale adoption is hindered by limited understanding of their charge storage mechanisms in different Zn-containing electrolytes. Here, we demonstrate the first synthesis of a MXene-derived Zn-preintercalated bilayered vanadium oxide (MD-ZVO) with a nanoflower-like morphology comprised of two-dimensional (2D) nanosheets, achieved via a two-step dissolution–recrystallization process. The strategic Zn2+ preintercalation establishes well-defined ion diffusion pathways, while the nanoflower-like assembly of 2D nanosheets enhances structural integrity, together contributing to improved electrochemical performance over other layered vanadium oxides. A systematic evaluation of four electrolytes (2 M ZnSO4, 2.6 M Zn(OTf)2, 2 M ZnCl2, and 30 m ZnCl2) showed that MD-ZVO electrodes delivered high reversible capacities (450 and 315 mAh g–1 at 0.1 A g–1), excellent rate capability (223 mAh g–1 for both electrolytes at 1.0 A g–1), and good electrochemical stability (84% and 48% over 1000 cycles at 1.0 A g–1) in saturated 2.6 M Zn(OTf)2 and highly concentrated 30 m ZnCl2, respectively. The material’s superior electrochemical stability in concentrated electrolytes is attributed to suppressed vanadium oxide dissolution during cycling. In situ and ex situ XRD analyses of MD-ZVO electrodes reveal larger contribution of Zn2+-associated species for charge storage in cells containing 2.6 M Zn(OTf)2 and proton dominant charge transfer in cells containing 30 m ZnCl2. Additionally, the combination of in situ and ex situ characterization demonstrates the reversible formation of ZnxOTfy(OH)2x–y·nH2O in cells using 2.6 M Zn(OTf)2 and Zn5(OH)8Cl2·H2O in cells using 30 m ZnCl2 on the MD-ZVO electrode surface over extended cycling. This work highlights the superior performance of nanoflower MD-ZVO for cathodes in aqueous Zn-ion batteries, which benefits from the proper selection of highly concentrated electrolytes that enable better utilization of the cathode material.
层状水合钒氧化物,特别是具有双层结构的水合钒氧化物,作为水合锌离子电池(AZIBs)的阴极具有显著的电化学性能。然而,由于对其在不同含锌电解质中的电荷存储机制了解有限,阻碍了它们的大规模应用。在这里,我们首次合成了mxene衍生的锌预插层双层氧化钒(MD-ZVO),其具有由二维(2D)纳米片组成的纳米花状形貌,通过两步溶解-再结晶工艺实现。战略性的Zn2+预插层建立了明确的离子扩散途径,而2D纳米片的纳米花样组装增强了结构完整性,共同有助于提高其他层状钒氧化物的电化学性能。对4种电解质(2 M ZnSO4, 2.6 M Zn(OTf)2, 2 M ZnCl2和30 M ZnCl2)的系统评价表明,MD-ZVO电极在饱和2.6 M Zn(OTf)2和高浓度30 M ZnCl2中分别具有高可逆容量(0.1 A g-1时450和315 mAh g-1),优异的倍率容量(1.0 A g-1时两种电解质223 mAh g-1)和良好的电化学稳定性(在1.0 A g-1下1000次循环84%和48%)。该材料在浓电解质中的优异电化学稳定性归功于循环过程中抑制了氧化钒的溶解。对MD-ZVO电极的原位和非原位XRD分析表明,在含有2.6 M Zn(OTf)2的电池中,Zn2+伴生物质对电荷存储的贡献更大,而在含有30 M ZnCl2的电池中,质子优势电荷转移的贡献更大。此外,原位和非原位表征的结合表明,在使用2.6 M Zn(OTf)2的电池中,Zn5(OH)8Cl2·H2O在使用30 M ZnCl2的电池中,经过长时间循环,Zn5(OH)8Cl2·H2O在MD-ZVO电极表面可逆形成。这项工作强调了纳米花MD-ZVO在水性锌离子电池阴极中的优越性能,这得益于正确选择高浓度电解质,从而更好地利用阴极材料。
期刊介绍:
ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.