表面缺陷诱导的单层MoS2纳米片在极性溶剂中的分散和稳定。

Chem & Bio Engineering Pub Date : 2025-05-16 eCollection Date: 2025-06-26 DOI:10.1021/cbe.4c00183
Yuxin Zhang, Yishu Chen, Zhengqi Peng, Deliang Wang, Chengzhi Fu, Pingwei Liu
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引用次数: 0

摘要

二维(2D)纳米片在极性溶剂中的有效分散对其实际应用至关重要。然而,通过机械剥离或液相剥离生产的超薄二硫化钼纳米片缺乏表面功能,这对实现均匀分散和良好的胶体稳定性提出了重大挑战。在此,我们研究了在纳米约束下自下而上合成的单层二硫化钼胶体的分散特性和稳定机制。纳米片在极性溶剂(如水、n -甲基吡罗烷酮和1,4-丁二醇)中达到了>1.6 g/L的高分散浓度,在乙二醇中最高浓度接近10.6 g/L,显著高于之前报道的浓度小于0.8 g/L的剥离二硫化钼纳米片。测定了MoS2纳米片的表面自由能为48.7 mJ/m2,由此可以准确预测其在各种溶剂中的最大稳定分散浓度。高表面自由能可归因于纳米片表面存在丰富的缺陷,这些缺陷诱导极性羟基(-OH)基团的形成,增加了表面的负电荷密度,从而增强了纳米片的分散性和胶体稳定性。这些发现对二维二硫化钼纳米片在各个领域的胶体应用具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surface Defect-Induced Dispersion and Stabilization of Monolayer MoS2 Nanosheets in Polar Solvents.

Effective dispersion of two-dimensional (2D) nanosheets in polar solvents is essential for their practical applications. However, ultrathin MoS2 nanosheets produced via mechanical exfoliation or liquid-phase exfoliation lack surface functionalities, posing a significant challenge for achieving a uniform dispersion and good colloidal stability. Here, we investigate the dispersion properties and stabilization mechanism of monolayer MoS2 colloids synthesized via a bottom-up strategy under nanoconfinement. The nanosheets achieve high dispersion concentrations of >1.6 g/L in polar solvents such as water, N-methylpyrrolidone, and 1,4-butanediol, with the highest concentration approaching 10.6 g/L in ethylene glycol, significantly higher than the previously reported concentrations of less than 0.8 g/L for the exfoliated MoS2 nanosheets. The surface free energy of our MoS2 nanosheets is determined to be 48.7 mJ/m2, from which their maximum stable dispersion concentrations in various solvents can be predicted precisely. The high surface free energy can be attributed to the presence of abundant surface defects on the nanosheets, which induce the formation of polar hydroxyl (-OH) groups and increase the negative charge density on the surface, thereby enhancing their dispersibility and colloidal stability. These findings hold significant implications for colloidal applications of 2D MoS2 nanosheets in various fields.

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