Organic-inorganic halide perovskite quantum dots (PQDs) constitute an attractive class of materials for many optoelectronic applications. However, their charge transport properties are inferior to materials like graphene. On the other hand, the charge generation efficiency of graphene is too low to be used in many optoelectronic applications. Here, we demonstrate the development of ultrathin phototransistors and photonic synapses using a graphene-PQD (G-PQD) superstructure prepared by growing PQDs directly from a graphene lattice. We show that the G-PQDs superstructure synchronizes efficient charge generation and transport on a single platform. G-PQD phototransistors exhibit excellent responsivity of 1.4 × 108 AW–1 and specific detectivity of 4.72 × 1015 Jones at 430 nm. Moreover, the light-assisted memory effect of these superstructures enables photonic synaptic behavior, where neuromorphic computing is demonstrated by facial recognition with the assistance of machine learning. We anticipate that the G-PQD superstructures will bolster new directions in the development of highly efficient optoelectronic devices.

The dielectric and other properties of a series of low-density polyimide block copolymer aerogels have been characterized. Two different anhydride-capped polyimide oligomers were synthesized: one from 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) and 4,4'-oxidianiline (ODA) and the other from biphenyl-3,3',4,4'-tetracarboxylic dianhydride and ODA. The oligomers were combined with 1,3,5-triaminophenoxybenzene to form a block copolymer networked structure that gelled in under 1 h. The polyimide gels were supercritically dried to give aerogels with relative dielectric constants as low as 1.08. Increasing the amount of 6FDA blocks by up to 50% of the total dianhydride decreased the density of the aerogels, presumably by increasing the free volume and also by decreasing the amount of shrinkage seen upon processing, resulting in a concomitant decrease in the dielectric properties. In this study, we have also altered the density independent of fluorine substitution by changing the polymer concentration in the gelation reactions and showed that the change in dielectric due to density is the same with and without fluorine substitution. The aerogels with the lowest dielectric properties and lowest densities still had compressive moduli of 4-8 MPa (40 times higher than silica aerogels at the same density), making them suitable as low dielectric substrates for lightweight antennas for aeronautic and space applications.

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Aerogels are one of the most interesting materials of the 21st century owing to their high porosity, low density, and large available surface area. Historically, aerogels have been used for highly efficient insulation and niche applications, such as interstellar particle capture. Recently, aerogels have made their way into the composite universe. By coupling nanomaterial with a variety of matrix materials, lightweight, high-performance composite aerogels have been developed for applications ranging from lithium-ion batteries to tissue engineering materials. In this paper, the current status of aerogel composites based on nanomaterials is reviewed and their application in environmental remediation, energy storage, controlled drug delivery, tissue engineering, and biosensing are discussed.

Graphene electrode–based supercapacitors are in high demand due to their superior electrochemical characteristics. A major bottleneck of using the supercapacitors for commercial applications lies in their inferior electrode cycle life. Herein, a simple and facile method to fabricate highly efficient supercapacitor electrodes using pristine graphene sheets vertically stacked and electrically connected to the carbon fibers which can result in vertically aligned graphene–carbon fiber nanostructure is developed. The vertically aligned graphene–carbon fiber electrode prepared by electrophoretic deposition possesses a mesoporous 3D architecture which enabled faster and efficient electrolyte‐ion diffusion with a gravimetric capacitance of 333.3 F g−1 and an areal capacitance of 166 mF cm−2. The electrodes displayed superlong electrochemical cycling stability of more than 100 000 cycles with 100% capacitance retention hence promising for long‐lasting supercapacitors. Apart from the electrochemical double layer charge storage, the oxygen‐containing surface moieties and α‐Ni(OH)2 present on the graphene sheets enhance the charge storage by faradaic reactions. This enables the assembled device to provide an excellent gravimetric energy density of 76 W h kg−1 with a 100% capacitance retention even after 1000 bending cycles. This study opens the door for developing high‐performing flexible graphene electrodes for wearable energy storage applications.

Anisotropic electrical conductivity was introduced into bulk polymer derived ceramics by embedded reduced graphene oxide aerogels.

Core-shell nanofibers containing poly(acrylic acid) (PAA) and manganese oxide nanoparticles as the core and polypyrrole (PPy) as the shell were fabricated through electrospinning the solution of PAA and manganese ions (PAA/Mn). The obtained nanofibers were stabilized by Fe through the interaction between Fe ions and carboxylate groups. Subsequent oxidation of Mn by KMnO produced uniform manganese dioxide (MnO) nanoparticles in the fibers. A PPy shell was created on the fibers by immersing the fibers in a pyrrole solution where the Fe ions in the fiber polymerized the pyrrole on the fiber surfaces. In the MnO@PAA/PPy core-shell composite fibers, MnO nanoparticles function as high-capacity materials, while the PPy shell prevents the loss of MnO during the charge/discharge process. Such a unique structure makes the composite fibers efficient electrode materials for supercapacitors. The gravimetric specific capacity of the MnO@PAA/PPy core-shell composite fibers was 564 F/g based on cyclic voltammetry curves at 10 mV/s and 580 F/g based on galvanostatic charge/discharge studies at 5 A/g. The MnO@PAA/PPy core-shell composite fibers also present stable cycling performance with 100% capacitance retention after 5000 cycles.

Polymer-derived ceramics (PDCs) are fabricated through the controlled pyrolysis of silicon-based polymeric precursors. Their structure, and subsequent material responses, are highly dependent on the chemistry of the pre-ceramic polymer, the...