MXene-Derived Potassium-Preintercalated Bilayered Vanadium Oxide Nanostructures for Cathodes in Nonaqueous K-Ion Batteries

IF 5.3 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Timofey Averianov, Xinle Zhang, Ryan Andris, Daniel Olds, Michael J. Zachman and Ekaterina Pomerantseva*, 
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Abstract

Bilayered vanadium oxides (BVOs) are promising cathode materials for beyond-Li-ion batteries due to their tunable chemistries and high theoretical capacities. However, the large size of beyond-Li+ ions limits electrochemical cycling and rate capability of BVO electrodes. Recent reports of MXene-derived BVOs with nanoscale flower-like morphology have shown improved electrochemical stability at high rates up to 5C in nonaqueous lithium-ion batteries. Here, we report how morphological stabilization can lead to improved rate capability in potassium-ion batteries (PIBs) through the synthesis and electrochemical characterization of MXene-derived K-preintercalated BVOs (MD-KVOs), which were derived from two V2CTx precursor materials prepared using two different etching protocols. We show that the etching conditions affect the surface chemistry of the MXene, which plays a role in the MXene-to-oxide transformation process. MXene derived from a milder etchant transformed into a nanoflower MD-KVO with two-dimensional (2D) nanosheet petals (KVO-DMAE) while a more aggressive etchant produced a MXene that transformed into a MD-KVO with one-dimensional (1D) nanorod morphology (KVO-CMAE). Electrochemical cycling of the produced MD-KVOs after drying at 200 °C under vacuum (KVO-DMAE-200 and KVO-CMAE-200) in PIBs showed that electrochemical stability of MD-KVO at high rates improved through the morphological stabilization of 2D particles combined with the control of interlayer water and K+ ion content. Structure refinement of KVO-DMAE-200 further corroborates the behavior observed during K+ ion cycling, connecting structural and compositional characteristics to the improved rate capability. This work demonstrates how proper synthetic methodology can cause downstream effects in the control of structure, chemical composition, and morphology of nanostructured layered oxide materials, which is necessary for development of future materials for beyond-Li-ion battery technologies.

mxene衍生的钾预插层双层氧化钒纳米结构在非水k离子电池中的应用
双层钒氧化物(BVOs)具有可调的化学性质和较高的理论容量,是超锂离子电池极具前景的正极材料。然而,超li +离子的大尺寸限制了BVO电极的电化学循环和速率能力。最近有报道称,mxene衍生的具有纳米级花状形态的BVOs在非水锂离子电池中表现出高达5C的电化学稳定性。在这里,我们通过mxene衍生的k -预插层BVOs (MD-KVOs)的合成和电化学表征,报道了形态稳定如何导致钾离子电池(PIBs)的速率性能提高,这些BVOs是由两种不同蚀刻方案制备的V2CTx前驱体材料制成的。我们发现蚀刻条件会影响MXene的表面化学性质,这在MXene向氧化物的转变过程中起作用。从温和的蚀刻剂中得到的MXene转化为具有二维(2D)纳米片花瓣的纳米花MD-KVO (KVO-DMAE),而更强的蚀刻剂产生的MXene转化为具有一维(1D)纳米棒形态的MD-KVO (KVO-CMAE)。在PIBs中对200°C真空干燥后制备的MD-KVO (KVO-DMAE-200和KVO-CMAE-200)进行电化学循环,结果表明,通过二维颗粒的形态稳定以及层间水分和K+离子含量的控制,MD-KVO的电化学稳定性得到了快速提高。KVO-DMAE-200的结构改进进一步证实了K+离子循环过程中观察到的行为,将结构和成分特征与提高的速率能力联系起来。这项工作证明了适当的合成方法如何在控制纳米结构层状氧化物材料的结构、化学成分和形态方面产生下游效应,这对于开发超越锂离子电池技术的未来材料是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.30
自引率
3.40%
发文量
1601
期刊介绍: ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. 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 applications of nanomaterials.
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