For graphene-based composites, the dynamics of polymers confined between graphene sheets are a key parameter governing the overall mechanical properties of bulk materials. Here, we used neutron reflectivity (NR) to measure the diffusion dynamics of polymer melts confined between graphene oxide (GO) surfaces. From the NR results, we found that the diffusion coefficients of poly(methyl methacrylate) (PMMA) between the GO sheets were dramatically reduced by more than 1 order of magnitude when the film thickness was less than ∼3 times the gyration radius of the bulk polymer (R g), whereas the diffusion of the polystyrene (PS) films sandwiched between GO sheets was only three times slower as the PS thickness decreased from ∼8 R g to 1 R g. This difference was due to the fact that the polymer-GO interaction significantly influences the dynamics of confined polymer melts.
We investigate the effect of adding graphene oxide (GO) sheets at the polymer-polymer interface on the dewetting dynamics and compatibility of immiscible polymer bilayer films. GO monolayers are deposited at the poly(methyl methacrylate) (PMMA)-polystyrene (PS) interface by the Langmuir-Schaefer technique. GO monolayers are found to significantly inhibit the dewetting behavior of both PMMA films (on PS substrates) and PS films (on PMMA substrates). This can be interpreted in terms of an interfacial interaction between the GO sheets and these polymers, which is evidenced by the reduced contact angle of the dewet droplets. The favorable interaction of GO with both PS and PMMA facilitates compatibilization of the immiscible polymer bilayer films, thereby stabilizing their bilayer films against dewetting. This compatibilization effect is verified by neutron reflectivity measurements, which reveal that the addition of GO monolayers broadens the interface between PS and the deuterated PMMA films by 2.2 times over that of the bilayer in the absence of GO.
Organic electrochromic (EC) materials are generally known to be electrochemically unstable during the ion intercalation/deintercalation process. One effective method to stabilize them is incorporating graphene derivatives in the polymer matrix, thereby creating strong interaction between graphene derivatives and polymer. However, previous studies are limited to specific polymers and bulk-blended systems, such as mixing the polymer with graphene derivatives. In this study, we developed a polymer-graphene derivative complex with the chemical assistance of a surfactant (octadecylamine, ODA). Graphene oxide (GO) was introduced as a protective layer on the electrochromic poly(3-hexyl thiophene) (P3HT) films by the Langmuir-Schaefer method. The deposition of the GO-ODA protective layer with high coverage was confirmed by atomic force microscopy and high-resolution X-ray reflectivity. The strong interactions between GO-ODA and P3HT were examined with UV-vis spectrophotometry and X-ray photoelectron spectroscopy. Electrochemical and electrochromic investigations revealed that the GO-ODA layer greatly improved the long-term cyclability of the P3HT film. These findings imply that the GO-ODA complex can significantly stabilize the EC cycling, due to its strong interaction with the P3HT film.
We present a simple and facile approach to creating asymmetrically modified graphene oxide sheets by grafting polymers with different polarities. Single-layered Janus graphene derivatives were prepared by grafting polymers with different polarities at the liquid–gas interface through one step functionalization. This approach allows obtaining free-standing monolayers of Janus graphene oxide sheets for large area, and also controlling the morphology (i.e., wrinkled Janus graphene oxide sheets) by a compression monolayer. A neutron reflectivity technique is used to check the functionalization on each side of the monolayer, and the results are compared with contact angles to determine its amphiphilic nature. The free-standing Janus monolayers become robust after UV-irradiation, and are able to withstand various solvents. Because these robust Janus graphene films can maintain their anisotropic functionalities over time, this technique provides a new strategy for fabricating functional materials that require amphiphilic properties (i.e., oil–water separation membranes and chemical compatibilizers functioning as a 2D surfactant) and different electrical functionalities (i.e., flexible lightweight p–n junction semiconductors and stimuli-driven actuators).
We have studied an orientation structure of self-assembled block copolymers (dPS-b-PMMA) of deuterated polystyrene (dPS) and poly(methyl methacrylate) (PMMA) confined between graphene oxide (GO) surfaces. The results of combination techniques, such as neutron reflectivity, time-of-flight secondary-ion mass spectrometry, grazing-incidence small-angle X-ray scattering, and scanning electron microscopy, show that self-assembled domains of the block copolymers in thin films near the GO sheets are oriented perpendicular to the surface of the GO monolayers, in contrast to the horizontal lamellar structure of the copolymer thin film in the absence of the GO monolayers. This is due to the amphiphilic nature of the GO, which leads to a nonpreferential interaction of both dPS and PMMA blocks. Double-sided confinement with the GO monolayers further extends the ordering behavior of the dPS-b-PMMA thin films. Continuous vertical orientation of the block copolymer thin films is also obtained in the presence of alternating GO layers within thick copolymer films.
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