通过嵌入分子薄的液体层,云母上的MoS2和WS2充放电的证据

H. Li, S. Kovalchuk, A. Kumar, D. Liang, B. Frank, H. Lin, N. Severin, K. Bolotin, S. Kirstein, J. P. Rabe
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摘要

过渡金属二硫化物(TMDC)通常在云母上机械剥离并在环境条件下检测。我们知道,在一定的相对湿度以上,一层分子薄的水穿插在云母和TMDC之间。在这里,我们研究了分子薄的液体层对MoS2和WS2在干燥云母上剥离并暴露于水、乙醇和四氢呋喃(THF)蒸气中的光谱的影响。干云母上的TMDCs的光致发光(PL)和差反射率(ΔR/R)光谱显示,n掺杂使TMDCs的trion发射占优势。水的插入消除了电荷掺杂,导致纯中性激子发射,而乙醇层可以与水可逆交换,不能完全抑制电荷。同样,原子力显微镜显示,THF介于TMDC和云母之间,但它不抑制云母的充电。在二硫化钼双层和三层中,插入的水层导致间接带跃迁的强度几乎增加了一倍。本文所描述的分子薄液体层对TMDCs的充放电可以为更好地控制TMDCs在环境条件下的光学性能提供重要线索。这篇文章受版权保护。版权所有。
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Evidence for charging and discharging of MoS2 and WS2 on mica by intercalating molecularly thin liquid layers
Transition metal dichalcogenides (TMDC) are often mechanically exfoliated on mica and examined under ambient conditions. It is known that above a certain relative humidity, a molecularly thin layer of water intercalates between the mica and the TMDC. Here, we investigate the effect of molecularly thin liquid layers on the optical spectra of MoS2 and WS2 exfoliated on dry mica and exposed to the vapors of water, ethanol, and tetrahydrofuran (THF). Photoluminescence (PL) and differential reflectance (ΔR/R) spectra on the TMDCs on dry mica show dominant trion emission due to n‐doping. Intercalation of water removes charge doping and results in purely neutral exciton emission, while an ethanol layer, which can be reversibly exchanged with water, does not completely suppress charge. Similarly, THF intercalates between TMDC and mica, as shown by atomic force microscopy, but it does not suppress the charging of mica. In MoS2 bi‐ and trilayers, an intercalated water layer leads to a near doubling of the intensity of the indirect band transition. The described charging/discharging of TMDCs by molecular thin liquid layers could provide important clues to better control the optical properties of TMDCs under environmental conditions.This article is protected by copyright. All rights reserved.
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