空气稳定二维WTe2材料封盖层的研制

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Aris Jansons, Andrejs Terehovs, Agnese Spustaka, Jevgenijs Gabrusenoks, George Chikvaidze, Anatolijs Sarakovskis and Gunta Kunakova*, 
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引用次数: 0

摘要

二维二碲化钨(2D WTe2)具有丰富多样的非常规性质,特别有希望用于拓扑非平凡态的基础研究及其在先进电子和量子技术中的潜在应用。考虑到未来的大多数应用依赖于稳定的电荷输运特性,WTe2在环境条件下对氧化的易感性提出了一个重大挑战,限制了它的实际应用。在这项研究中,我们提出了一种创新的无机聚硅氮烷覆盖层,它可以转化为二氧化硅,有效地将二维WTe2结构与氧气和水隔离。此外,还测试了正己胺对WTe2表面的钝化作用。低温下生长、聚硅氮烷封盖和正己胺功能化结构的电荷输运测量表明,所开发的无机聚硅氮烷封盖层有效地保护了环境环境中的氧化,从而使2D WTe2在较长时间内保持其结构完整性和电子特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Capping Layer for Air-Stable 2D WTe2 Materials

Two-dimensional tungsten ditelluride (2D WTe2) possesses a rich variety of unconventional properties, which are particularly promising for fundamental studies of topologically nontrivial states and their potential applications in advanced electronics and quantum technologies. Given that the majority of future applications rely on stable charge transport characteristics, the susceptibility of WTe2 to oxidation under ambient conditions presents a significant challenge, limiting its practical use. In this study, we present an innovative inorganic polysilazane capping layer that can be converted to silica to effectively isolate 2D WTe2 structures from oxygen and water. Additionally, WTe2 surface passivation with n-hexylamine is also tested. Charge transport measurements at low temperatures for as-grown, polysilazane-capped, and n-hexylamine-functionalized structures demonstrate that the developed inorganic polysilazane capping layer efficiently protects from oxidation in an ambient environment, thereby allowing 2D WTe2 to maintain its structural integrity and electronic characteristics over extended periods.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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