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Synthesis of 2D Solid-Solution (NbyV2–y)CTx MXenes and Their Transformation into Oxides for Energy Storage

MXenes公司 材料科学 氧化物 氧化钒 化学工程 电化学 氧化铌 无定形固体 电极 X射线光电子能谱 纳米技术 无机化学 化学 物理化学 结晶学 冶金 工程类
作者
Marcelo A. Andrade,Timofey Averianov,Christopher E. Shuck,Kateryna Shevchuk,Yury Gogotsi,Ekaterina Pomerantseva
出处
期刊:ACS applied nano materials [American Chemical Society]
卷期号:6 (18): 16168-16178 被引量:5
标识
DOI:10.1021/acsanm.3c02004
摘要

Vanadium and niobium oxides have been identified as promising electrodes for electrochemical energy storage applications as their constituent transition metals can undergo multiple reduction steps leading to high specific capacities during cycling. MXenes are attractive precursors for these compounds due to their tunable compositions and 2D nanoscale morphology. Herein, we demonstrate the synthesis of a wide range of solid-solution (NbyV2–y)AlC MAX phases, their chemical etching to produce (NbyV2–y)CTx MXenes, and the subsequent oxidation of MXenes to form respective oxides. We show that the formation of solid solutions facilitated the etching kinetics of MAX phase powder and accelerated MXene formation compared to pure vanadium and niobium carbides. Oxidation of V2CTx and Nb2CTx produced bilayered vanadium oxide (BVO) with a crumpled nanosheet morphology and nanostructured amorphous Nb2O5 (nANO) nanospheres, respectively. For oxides derived from solid-solution MXenes, scanning electron microscopy imaging revealed the growth of nANO on the surface of BVO nanosheets. Electrochemical cycling of (NbyV2–y)CTx-derived oxides in Li-ion cells revealed varying intercalation-like behavior with electrodes derived from V2CTx showing redox processes and nANO exhibiting pseudocapacitive response. The CV curves of solid-solution MXene-derived oxides demonstrated primarily BVO/nANO composite-like behavior, with key exceptions. The cells containing Nb0.25V1.75CTx-derived oxide showed a large capacity of 296.8 mA h g–1 driven by significant electrochemical activity at all potentials along the sweep possibly stemming from niobium doping into BVO structure. The Nb1.00V1.00CTx-derived oxide electrode delivered a specific capacity of 298 mA h g–1 with contributions from both, BVO and nANO phases. The improved electrochemical stability of (Nb1.00V1.00)CTx-derived oxide electrodes compared to an electrode prepared by physically mixing Nb2CTx-derived oxide with V2CTx-derived oxide with the same Nb/V molar ratio was attributed to the stabilizing effect of the BVO/nANO heterointerface. Our work indicates that the use of solid-solution MXenes as precursors is an attractive strategy to synthesize oxides with compositions, morphologies, and properties that cannot be produced otherwise.

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