Sustainability urgently demands low dielectric loss and low elastic modulus as fostering high permittivity (Hi-K) conductor/polymer composites. This work introduces a ternary composite system, consisting of acrylic resin elastomer (AR), chemically modified polyaniline (HBSiPA), and the thermally reduced graphene oxides (TrGOs), for applying to actuators, of which AR was fabricated by free radical polymerization. The unique hybridized graphene (HBSiPA-TrGO) was prepared by a two-step procedure, including the doped polyaniline modified by the hyperbranched polysiloxane via a ring opening reaction, followed by the decoration of HBSiPA on the surface of TrGO, the conductivity of which is desired to be the same as that of graphene. Afterward, diverse filler contents of HBSiPA-TrGO were put into the AR matrix to fabricate composites with the solution casting method and TrGO/AR composites were fabricated as well for comparison. Unlike TrGO, HBSiPA has plenty of polyaniline chain segments that ensure better dispersion of graphene hybrids in the AR, and thus the composites inherit the excellent electrical property of graphene. The permittivity and dielectric loss of the HBSiPA-TrGO/AR composite at 100 Hz are 3.5 and 0.27 times that of the TrGO/AR composite, respectively, when the loading of fillers approaches the percolation threshold (f), which originates from the HBSiPA anchored onto the graphene serving as spacer and thus decreases the leakage currents induced by the contact of graphene sheets. Besides, the elastic modulus of 2.83 vol % HBSiPA-TrGO/AR composite was lower than 5 MPa.
Carbon dots (CDs) are synthesized by the solvothermal method with four kinds of solvents including water, dimethylformamide (DMF), ethanol, and acetic acid (AA). The aqueous solutions of the above CDs emit multiple colors of blue (470 nm), green (500 nm), yellow (539 nm), and orange (595 nm). The structures, sizes, and chemical composition of the CDs are characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS). The optical properties of multicolored CDs are analyzed by UV−vis absorption and photoluminescence (PL) spectra. It has been revealed that DMF is the key solvent to synthesized CDs for the red shift of fluorescence emission, which could be enhanced by adding an AA solvent. The structures of functional groups such as the contents of graphitic N in carbon cores and oxygencontaining functional groups on the surface of CDs are affected by these four solvents. According to the oxidation and selective reduction of NaBH 4 , the implication for multicolor imaging has been discussed based on the COOH, C−O−C, and CO functional groups.
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