Synthesis and characterization of MoSe2 nanoscrolls via pulsed laser ablation in deep eutectic solvents†

IF 5.1 3区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Nanoscale Pub Date : 2024-05-28 DOI:10.1039/D4NR01466A
Alejandro L. Morales Betancourt, Sadasivan Shaji, Ernesto Flores and Kelly L. Nash
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引用次数: 0

Abstract

There is ongoing interest in the rapid, reproducible production of 2-dimensional (2-D) transition metal dichalcogenides (TMD), such as molybdenum-based TMD (MoX2), where X is a chalcogen atom such as sulphur (S), selenium (Se) or tellurium (Te), driven by their unique optical and electronic properties. Once fabricated into an atomically thin layer structure, these materials have a direct-indirect bandgap transition, strong spin–orbit coupling, and favourable electronic and mechanical strain-dependent properties which are attractive for electronics. Pulsed laser ablation in liquid (PLAL) is an economic, green alternative for synthesis of TMD. It has been shown that in the case of MoX2, the chemical processes during the plasma phase of the ablation can yield the formation of multispecies, including MoOx quantum dots when oxygen-containing solvents are used. Here, we introduce the formation of MoSe2 nanoscrolls with low oxygen content synthesized via pulsed laser ablation in deep eutectic solvents (PLADES). Our results suggest that the synthesis produces a stable colloidal solution of large 2-D structures with tuneable surface charge by replacing the deep eutectic solvent (DES) with DI water. Nuclear Magnetic Resonance (NMR) results suggest that irradiating the solvent at near infrared NIR energy does not affect its chemical composition. NMR also proves that serial washing can completely remove solvent from the nanostructures. Raman shifts suggest the formation of large, thin MoSe2 nanosheets aided by the solvent confinement resulting from van der Waal forces and hydrogen bonds interactions between MoSe2 and urea. Binding energies measured by X-ray photoelectron spectroscopy (XPS) confirm MoSe2-DES preference to form 1T-MoSe2versus molybdenum oxides and 2H MoSe2 in DI-water. Raman and XPS findings were validated by transmission electron microscopy (TEM) and selected area electron diffraction (SAED). Results of this work validate the use of PLADES for the synthesis of stable, crystalline, low-surface-oxygen-content colloidal MoSe2 nanoscrolls in scalable quantities.

Abstract Image

在深共晶溶剂中通过脉冲激光烧蚀合成 MoSe2 纳米卷并确定其特性
二维过渡金属二掺杂物(TMD)(如钼基 TMD(MoX2),其中 X 为合钙原子,如硫(S)、硒(Se)或碲(Te)))的独特光学和电子特性推动了二维过渡金属二掺杂物(TMD)的快速、可重复生产。一旦制作成原子级薄层结构,这些材料就具有直接-间接带隙转变、强自旋轨道耦合以及有利的电子和机械应变特性,对电子产品具有吸引力。液态脉冲激光烧蚀(PLAL)是合成 TMD 的一种经济、绿色的替代方法。研究表明,在 MoX2 的情况下,使用含氧溶剂时,烧蚀等离子体阶段的化学过程可以形成多物种,包括 MoOx 量子点。在这里,我们介绍了在深共晶溶剂(PLADES)中通过脉冲激光烧蚀合成的低氧含量 MoSe2 纳米卷的形成。我们的研究结果表明,通过用去离子水代替深共晶溶剂(DES),该合成方法可产生具有可调表面电荷的大型二维结构的稳定胶体溶液。核磁共振(NMR)结果表明,用近红外 NIR 能量照射溶剂不会影响其化学成分。核磁共振还证明,连续清洗可以完全去除纳米结构中的溶剂。拉曼偏移表明,在 Mose2 和尿素之间的范德华力和氢键相互作用产生的溶剂约束的帮助下,形成了大而薄的 MoSe2 纳米片。通过 XPS 测量的结合能证实,在去离子水中,MoSe2-DES 与钼氧化物和 2H MoSe2 相比更倾向于形成 1T-MoSe2。透射电子显微镜(TEM)和选区电子衍射(SAED)验证了拉曼和 XPS 的发现。这项工作的结果验证了 PLADES 可用于合成稳定、结晶、低表面氧含量、可扩展数量的胶体 MoSe2 纳米卷。
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来源期刊
Nanoscale
Nanoscale CHEMISTRY, MULTIDISCIPLINARY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
12.10
自引率
3.00%
发文量
1628
审稿时长
1.6 months
期刊介绍: Nanoscale is a high-impact international journal, publishing high-quality research across nanoscience and nanotechnology. Nanoscale publishes a full mix of research articles on experimental and theoretical work, including reviews, communications, and full papers.Highly interdisciplinary, this journal appeals to scientists, researchers and professionals interested in nanoscience and nanotechnology, quantum materials and quantum technology, including the areas of physics, chemistry, biology, medicine, materials, energy/environment, information technology, detection science, healthcare and drug discovery, and electronics.
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