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表面缺陷诱导的单层二硫化钼纳米片在极性溶剂中的分散与稳定

Surface Defect-Induced Dispersion and Stabilization of Monolayer MoS Nanosheets in Polar Solvents.

作者信息

Zhang Yuxin, Chen Yishu, Peng Zhengqi, Wang Deliang, Fu Chengzhi, Liu Pingwei

机构信息

State Key Laboratory of Chemical Engineering and Low-Carbon Technology, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, P. R. China.

Institute of Zhejiang University - Quzhou, 99 Zheda Road, Quzhou 324000, P. R. China.

出版信息

Chem Bio Eng. 2025 May 16;2(6):370-379. doi: 10.1021/cbe.4c00183. eCollection 2025 Jun 26.

Abstract

Effective dispersion of two-dimensional (2D) nanosheets in polar solvents is essential for their practical applications. However, ultrathin MoS 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 MoS 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, -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 MoS nanosheets. The surface free energy of our MoS nanosheets is determined to be 48.7 mJ/m, 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 MoS nanosheets in various fields.

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制备的超薄MoS纳米片缺乏表面官能团,这对实现均匀分散和良好的胶体稳定性构成了重大挑战。在此,我们研究了在纳米限域条件下通过自下而上策略合成的单层MoS胶体的分散性质和稳定机制。这些纳米片在水、N-甲基吡咯烷酮和1,4-丁二醇等极性溶剂中实现了>1.6 g/L的高分散浓度,在乙二醇中的最高浓度接近10.6 g/L,显著高于之前报道的剥离MoS纳米片小于0.8 g/L的浓度。我们的MoS纳米片的表面自由能被测定为48.7 mJ/m²,据此可以精确预测它们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上存在丰富的表面缺陷,这些缺陷诱导形成极性羟基(-OH)基团并增加表面负电荷密度,从而增强其分散性和胶体稳定性。这些发现对二维MoS纳米片在各个领域的胶体应用具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e052/12207278/68f2dd3e74ab/be4c00183_0001.jpg

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