A Thermodynamic Perspective on Liquid Phase Exfoliation of Two Dimensional Van der Waals Solids
Pieter Schiettecatte a, Zeger Hens a
a Physics and Chemistry of Nanostructures, Department of Chemistry, Ghent University, Belgium, Krijgslaan 281 - S3, Ghent, Belgium
Materials for Sustainable Development Conference (MATSUS)
Proceedings of nanoGe Fall Meeting 2021 (NFM21)
#NCFun21. Fundamental Processes in Nanocrystals and 2D Materials
Online, Spain, 2021 October 18th - 22nd
Organizers: Brandi Cossairt and Jonathan De Roo
Contributed talk, Pieter Schiettecatte, presentation 202
DOI: https://doi.org/10.29363/nanoge.nfm.2021.202
Publication date: 23rd September 2021

Liquid phase exfoliation (LPE) offers a scalable method to prepare colloids of two-dimensional (2D) Van der Waals (VdW) solids. Over the years, LPE has been rationalized within the context of solution thermodynamics. We outline this approach by introducing a method for the LPE of rhenium disulfide (ReS2), a promising novel semiconducting 2D material. By screening LPE in various solvents, we retrieve optimal conditions for high yield ReS2 exfoliation in solvents characterized by similar Hildebrand and Hansen solubility parameters – a result in agreement with the solution thermodynamics approach. Besides, our thermodynamic analysis points out that the current method to describe LPE fails to account for the considerable tolerance on the solubility parameter mismatch. In other words, the window for solvent exfoliation is much broader than solution thermodynamics allows for based on the size of the colloid.

We combine our experimental dataset on ReS2 with an extensive survey of literature studies to reconcile the too-broad exfoliation window observed for 2D VdW solids. Starting from standard Flory-Huggins theory, we address inconsistencies in the current line of thought and propose a more coherent way of working based on the critical exchange parameter χc – an idea inspired by polymer physics. In such a framework, suitable exfoliation solvents result in exchange parameters below a critical value χc. Notably, the predicted solubility parameter window for suitable exfoliation solvents based on such a criterium agrees well with the experimental data available for a wide range of 2D VdW solids. Therefore, we conclude that solution thermodynamics describes LPE, provided that the solubility parameter window is linked to the critical exchange parameter for solvent/solute immiscibility.

P.S. acknowledges the FWO-Vlaanderen for a fellowship (FWO-SB scholarship, FWO Project
Number: 1S40117N), Z.H. acknowledges Ghent University (GOA 01G01019) and the FWO-
Vlaanderen (G0F0920N) for funding.

© FUNDACIO DE LA COMUNITAT VALENCIANA SCITO
We use our own and third party cookies for analysing and measuring usage of our website to improve our services. If you continue browsing, we consider accepting its use. You can check our Cookies Policy in which you will also find how to configure your web browser for the use of cookies. More info