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      Viscous fingering instabilities in spontaneously formed blisters of MoS 2 multilayers†

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      a , a , b , , a ,
      Nanoscale Advances
      RSC

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          Abstract

          The viscous fingering in the Hele-Shaw cell can be suppressed by replacing the upper-bounding rigid plate with an elastic membrane. Recently, graphene multilayers while polymer-curing-induced blistering showed the dynamical evolution of viscous fingering patterns on a viscoelastic substrate due to their thickness-dependent elasticity. Under certain conditions, the elastic solid-based instability couples with the viscoelastic substrate-based instability. The mechanisms underlying such a coupling in the blisters of 2D materials and the dynamical evolution of the viscous fingering patterns underneath the blisters are yet to be addressed. Herein, we investigate the viscous fingering instabilities in spontaneously formed blisters of MoS 2 multilayers, and provide thorough analytical and experimental insights for the elucidation of the dynamical evolution of the viscous fingering patterns and the coupled instabilities in the blisters. We also estimate the interfacial adhesion energy of the MoS 2 flakes over a (poly)vinyl alcohol (PVA) substrate and the confinement pressure inside the MoS 2 blisters using a conventional blister-test model. It is observed that the presence of instability gives rise to anomalies in the modeling of the blister test. The adhesion mechanical insights would be beneficial for fundamental research as well as practical applications of 2D material blisters in flexible optoelectronics.

          Abstract

          A schematic representation of PVA-curing-induced blistering of MoS 2 multilayers with and without the adsorption of tiny ice-water droplets (mist) over the PVA-coated Pyrex substrate prior to the mechanical exfoliation step.

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          Ultrastrong adhesion of graphene membranes

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            The Penetration of a Fluid into a Porous Medium or Hele-Shaw Cell Containing a More Viscous Liquid

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              Universal shape and pressure inside bubbles appearing in van der Waals heterostructures

              Trapped substances between a two-dimensional (2D) crystal and an atomically flat substrate lead to the formation of bubbles. Their size, shape and internal pressure are determined by the competition between van der Waals attraction of the crystal to the substrate and the elastic energy needed to deform it, allowing to use bubbles to study elastic properties of 2D crystals and conditions of confinement. Using atomic force microscopy, we analysed a variety of bubbles formed by monolayers of graphene, boron nitride and MoS2. Their shapes are found to exhibit universal scaling, in agreement with our analysis based on the theory of elasticity of membranes. We also measured the hydrostatic pressure induced by the confinement, which was found to reach tens of MPa inside submicron bubbles. This agrees with our theory estimates and suggests that for even smaller, sub-10 nm bubbles the pressure can be close to 1 GPa and may modify properties of a trapped material.
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                Author and article information

                Journal
                Nanoscale Adv
                Nanoscale Adv
                NA
                NAADAI
                Nanoscale Advances
                RSC
                2516-0230
                30 October 2023
                21 November 2023
                30 October 2023
                : 5
                : 23
                : 6617-6625
                Affiliations
                [a ] Department of Physics, Indian Institute of Technology Ropar Rupnagar Punjab-140001 India rakesh@ 123456iitrpr.ac.in rajeev.ahuja@ 123456iitrpr.ac.in
                [b ] Condensed Matter Theory Group, Department of Physics and Astronomy, Uppsala University Box 516 Uppsala-75120 Sweden rajeev.ahuja@ 123456physics.uu.se
                Author information
                https://orcid.org/0000-0002-6909-8814
                https://orcid.org/0000-0003-1231-9994
                https://orcid.org/0000-0002-6892-5080
                Article
                d3na00563a
                10.1039/d3na00563a
                10662142
                c5d7b92a-c50d-42a7-a34f-7f67aec24519
                This journal is © The Royal Society of Chemistry
                History
                : 27 July 2023
                : 5 October 2023
                Page count
                Pages: 9
                Funding
                Funded by: Ministry of Education, India, doi 10.13039/501100004541;
                Award ID: Unassigned
                Funded by: Vetenskapsrådet, doi 10.13039/501100004359;
                Award ID: VR-2020-04410
                Award ID: VR-2021-00665
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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