Zhi-Guo Jiang

Functionalization and reduction of graphene oxide with p-phenylene diamine for electrically conductive and thermally stable polystyrene composites

A facile and efficient approach was developed to simultaneously functionalize and reduce graphene oxide (GO) with p-phenylene diamine (PPD) by simple refluxing. This was possible by the nucleophilic substitution reaction of epoxide groups of GO with amine groups of PPD aided by NH(3) solution. As a consequence, electrical conductivity of GO-PPD increased to 2.1 × 10(2) S/m, which was nearly 9 orders of magnitude higher than that of GO. Additionally, after the incorporation of GO-PPD in polystyrene (PS), the composites exhibited a sharp transition from electrically insulating to conducting behavior with a low percolation threshold of ~0.34 vol %, which was attributed to the improved dispersion and the reduction of GO-PPD. Thermal stability of the PS/GO-PPD composite was also ~8 °C higher than that of PS.

Simultaneous functionalization and reduction of graphene oxide with polyetheramine and its electrically conductive epoxy nanocomposites

Simultaneous functionalization and reduction of graphene oxide (GO) is realized by refluxing of GO suspension with polyetheramine (D2000) followed by thermal treatment at 120 °C. Compared to GO, the D2000-treated GO (GO-D2000) becomes hydrophobic, thermally stable and highly conductive with an electrical conductivity of 11 S/m, which is almost 8 orders of magnitude higher than that of GO. Due to the high conductivity and improved dispersion of GO-D2000, its epoxy nanocomposites exhibit a sharp transition from electrically insulating to conducting with a low percolation threshold of 0.71 vol%. With 3.6 wt% GO-D2000, the glass transition temperature of the epoxy nanocomposite is 27 K higher than that of neat epoxy.

Vertically Aligned High-Quality Graphene Foams for Anisotropically Conductive Polymer Composites with Ultrahigh Through-Plane Thermal Conductivities

Although graphene-based thermal interface materials (TIMs) have great potentials in removing excess heat generated during highly efficient running of electronic devices, their practical applications are usually limited by their unsatisfactory thermal conductions, which are mainly caused by unsatisfactory dispersion and distribution, low loading, and low quality of graphene sheets, as well as the thermal interfacial resistance between graphene sheets and polymer matrix. Herein, we develop vertically aligned graphene hybrid foams (GHFs) with high densities by hydrothermal reduction of graphene oxide in the presence of high-quality graphene nanoplatelets (GNPs) followed by air-drying. The reduced graphene oxide sheets play an important role in constructing a vertically aligned interconnection network for accommodating GNPs during the hydrothermal reduction process, while the incorporated GNPs not only make the thermal conductance network denser but also prevent excessive shrinkage of the foams during air-drying. More critically, graphitization of GHF at 2800 °C removes the residual oxygen-containing groups and heals the defects of their reduced graphene oxide component, leading to high-quality graphene foams. The resultant vertically aligned high-quality graphene porous architecture with high density as an ideal thermal conductance network of TIMs is highly efficient in improving the thermal conductivity of its epoxy composite, which exhibits an ultrahigh through-plane thermal conductivity of 35.5 W m-1 K-1 at a graphene loading of 19.0 vol %. The excellent thermally conductive performance makes the annealed GHF/epoxy composites suitable for the thermal management.

Rapidly Responsive and Flexible Chiral Nematic Cellulose Nanocrystal Composites as Multifunctional Rewritable Photonic Papers with Eco-Friendly Inks

Rapidly responsive and flexible photonic papers are manufactured by coassembly of cellulose nanocrystals (CNCs) and waterborne polyurethane (WPU) latex for fully taking advantage of the chiral nematic structure of CNCs and the flexibility of WPU elastomer. The resulting CNC/WPU composite papers exhibit not only tunable iridescent colors by adjusting the helical pitch size, but also instant optical responses to water and wet gas, ascribed to the easy chain movement of the elastomeric WPU that does not restrict the fast water absorption-induced swelling of CNCs. By choosing water or NaCl aqueous solutions as inks, the colorful patterns on the CNC/WPU photonic paper can be made temporary, durable, or even disguisable. In addition, the photonic paper is simultaneously rewritable for all these three types of patterns, and the disguisable patterns, which are invisible at normal times and show up under stimuli, exhibit a quick reveal conversion just by exhaling on the paper. The rewritability, rapid responsibility, easy fabrication, and the eco-friendly nature of the inks make the flexible photonic paper/ink combination highly promising in sensors, displays, and photonic circuits.