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The role of ionic liquid breakdown in the electrochemical metallization of VO <sub/>2</sub> : An NMR study of gating mechanisms and VO <sub/>2</sub> reduction

DOI:10.1021/jacs.8b09513 期刊:Journal of the American Chemical Society 出版年份:2018 更新时间:2025-09-23 15:21:21
摘要: Metallization of initially insulating VO2 via ionic liquid electrolytes, otherwise known as electrolyte gating, has recently been a topic of much interest for possible applications such as Mott transistors and memory devices. It is clear that the metallization takes place electrochemically and, in particular, there has previously been extensive evidence for the removal of small amounts of oxygen during ionic liquid gating. Hydrogen intercalation has also been proposed, but the source of the hydrogen has remained unclear. In this work, solid-state magic angle spinning NMR spectroscopy (1H, 2H, 17O and 51V) is used to investigate the thermal metal-insulator transition in VO2, before progressing to catalytically hydrogenated VO2 and electrochemically metallized VO2. In these experiments electrochemical metallization of bulk VO2 particles is shown to be associated with intercalation of hydrogen, the degree of which can be measured with quantitative 1H NMR spectroscopy. Possible sources of the hydrogen are explored, and by using a selectively deuterated ionic liquid, it is revealed that the hydrogenation is due to deprotonation of the ionic liquid; specifically, for the commonly used dialkyl-imidazolium based ionic liquids, it is the “carbene” proton which is responsible. Increasing the temperature of the electrochemistry is shown to increase the degree of hydrogenation, forming first a less hydrogenated metallic orthorhombic phase then a more hydrogenated insulating Curie-Weiss paramagnetic orthorhombic phase, both of which were also observed for catalytically hydrogenated VO2. The NMR results are supported by magnetic susceptibility measurements, which corroborate the degree of Pauli and Curie-Weiss paramagnetism. Finally, NMR spectroscopy is used to identify the presence of hydrogen in an electrolyte gated thin film of VO2, suggesting that electrolyte breakdown, proton intercalation and reactions with decomposition products within the electrolyte should not be ignored when interpreting the electronic and structural changes observed in electrochemical gating experiments.
作者: Michael A. Hope,Kent J. Griffith,Bin Cui,Fang Gao,Sian E. Dutton,Stuart S. P. Parkin,Clare P. Grey
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Investigating the role of ionic liquid breakdown in the electrochemical metallization of VO2 and exploring the gating mechanisms and VO2 reduction through NMR study.

Electrochemical metallization of VO2 with imidazolium ionic liquids is associated with hydrogen intercalation, primarily from the deprotonation of the ionic liquid's carbene hydrogen. This process can be controlled by temperature, leading to different phases of hydrogenated VO2. The findings suggest that electrolyte breakdown and proton intercalation play significant roles in the electronic and structural changes observed in electrochemical gating experiments.

The study is limited by the sensitivity of NMR spectroscopy, especially in detecting hydrogen in thin films, and the complexity of interpreting NMR shifts in paramagnetic and metallic materials. The electrochemical experiments' efficiency is also limited by competing side reactions.

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