Abstract

While the demand for lightweight high-strength nanocomposites is immense, their progress has been severely limited due to inferior filler dispersion and filler–matrix interface adhesion. This article reports a novel modification of graphene oxide (GO) encapsulated by the copolymer of polydopamine (PD) and polyethylenimine (PEI) via a Michael addition reaction, aiming to create robust ethylene vinyl acetate copolymer (EVA) nanocomposites even at very low amounts of filler loading by overcoming the above hindrances. It has been found that the addition of only 1.2 wt% modified GO (i.e., PD–PEI–rGO) increased the tensile strength, Young's modulus and storage modulus of EVA composites by 80%, 50% and 24%, respectively. These increments surpass many recent claims on relevant composites. Excellent molecular level dispersion was also observed from the fracture surface SEM images. Being amine-rich with high electron-donating capability and mechanically robust, the nanocomposite served as an outstanding tribopositive material, thereby generating 7.49 V and 4.06 μA output voltage and current, respectively, when employed in a triboelectric nanogenerator (TENG). The high electrical outputs led the device to light up 43 blue LEDs instantaneously upon hand pressing, demonstrating that the nanocomposite is indeed a promising candidate for harvesting green energy. Moreover, the nanogenerator displayed outstanding cyclic performance stability (even after 8000 cycles) and environmental durability.

Highlights

  • Reproducing the same voltage signals when tested a er 21 days under similar mechanical force. These results clearly indicated that the PD–PEI–rGO/ethylene vinyl acetate copolymer (EVA) nanocomposite is literally very strong and robust

  • We reported a novel and effective approach for graphene oxide (GO) modi cation to produce mechanically strong EVA nanocomposites with multifunctional capability

  • The surface modi cation was carried out by a unique mussel-inspired polydopamine-assisted Michael addition reaction. This approach showed greater promise in terms of molecular level dispersion and the interface adhesion of graphene nanosheets within the EVA matrix owing to strong hydrogen bonding interactions

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Summary

Introduction

Among a variety of polymer nanocomposites, polymer–carbon nanomaterial composites, especially carbon nanotubes (CNTs) and graphene-based ones, are of the highest priority of current research interests as they deliver high electrical, thermal, mechanical and barrier properties to the composites at significantly low amounts.[1,2,3,4] While graphene is an atomically thick, 2-D sheet material composed of sp[2] carbon atoms arranged in a honeycomb structure, CNTs are zero-dimensional cylindrically rolled sheets of graphene.[5,6] Since 2004, the successful production and isolation of graphene[7] have taken the nanotechnology sector by storm, with exponential growth in its applications. This article aims to design a novel surface modi cation process for graphene oxide (GO) in order to develop mechanically stronger polymer nanocomposites even at signi cantly low amounts of loading. GO was selected, as it is 2444 | Nanoscale Adv., 2019, 1, 2444–2453

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