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Build a Rigid-Flexible Graphene/Silicone Interface by Embedding SiO₂ for Adhesive Application.

ABSTRACT: An effective strategy was developed to enhance the adaptability of graphene/silicone matrices under external stimuli by embedding nanoscale SiO₂ into the graphene/silicone interfaces as a buffer layer. Chemically reduced graphene (rGE) was first covered by SiO₂ using an in situ preparation, forming sandwichlike rGE/SiO₂ (rGES). Then, rGES was integrated into methyl vinyl polysiloxane, followed by vulcanization, producing the final rGES/silicone rubber (SR) nanocomposite. Such interfacial modification actually built a rigid-flexible SiO₂ buffer layer between rGE and polysiloxane. Obvious improvements were seen in both thermal and mechanical properties due to improved interfacial interaction. In a vulcanized rGES/SR system, the addition of 30 wt % rGES (3 wt % rGE) yielded a tensile strength of 6.13 MPa (up to 25 times that of the unmodified rGE in filled SR), a tear strength of 18.08 kN/m, and an elongation at break of 267%, several times higher than those of an rGE/SR nanocomposite. Thermal analysis results indicated that the initial decomposition temperature of rGES/SR containing 5 wt % rGES (0.5 wt % rGE) increased by more than 98 and 288 °C compared to that of SiO₂/SR and rGE/SR, respectively. The rGES/polysiloxane matrices showed a tensile shear adhesive strength of 1.78 MPa when used as an adhesive for aluminum sheets, which is higher than that of the rGE/polysiloxane matrix (0.93 MPa).

SUBMITTER: Wang H

PROVIDER: S-EPMC6640933 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Intermolecular interactions between the constituents of a polymer nanocomposite at the polymer-particle interface strongly affect the segmental mobility of polymer chains, correlated with their glass transition behavior, and are responsible for the improved dynamical viscoelastic properties. In this work, we emphasized on the evolution of characteristic interfaces and their dynamics in silica (SiO2 NP)-reinforced, solution-polymerized, styrene butadiene rubber (SSBR) composites, whose relative prevalence varied with the phosphonium ionic liquid (PIL) volume fraction, used as an interfacial modifier. The molecular origins of such interfaces were examined through systematic dielectric spectroscopy, molecular dynamics (MD) simulations, and dynamic-mechanical analyses. The PIL facilitated H-bonding, cation-π, surface-phenyl, and van der Waals interfacial interactions between SSBR and SiO2 NP, thereby regulating the polymer chain dynamics, orientation, and mean-square displacement. Specifically, the mass density profiles from MD simulations revealed the dynamic gradient of polymer chains in the interfacial region as a function of radial distance from the center of mass of the SiO2 NP surface. The results showed a structuring effect to result in well-resolved density peaks at specific radial distances with the tangential orientation of styrene monomers in the vicinity of the SiO2 NP surface. These domino effects highlighted strong interfacial interactions to have an indispensable effect on the viscoelastic performance and thermal motion of SSBR molecular chains, leading to a higher glass transition temperature (T g) by ∼15 K, validating the experimental data. More importantly, our results gave new insights into the fundamental understanding of the fact that the strength of intermolecular interactions induced by PIL at the polymer-particle interface is the key to control the α-relaxation dynamics and T g optimization, desired for specific applications.

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Build a Rigid-Flexible Graphene/Silicone Interface by Embedding SiO2 for Adhesive Application.

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Build a Rigid-Flexible Graphene/Silicone Interface by Embedding SiO₂ for Adhesive Application.