Polyaniline‐capped mesoporous carbon nanosheets with high conductivity and porosity are synthesized by vapor deposition polymerization. The mesoporous carbon template is prepared by removing ordered cubic iron oxide nanocrystals embedded in the carbon matrix obtained by thermal decomposition of an iron‐oleate complex in a sodium chloride matrix. The evaporated aniline monomers are slowly polymerized on the carbon surface pretreated with FeCl₃ as an initiator, partially filling the carbon pores to improve conductivity. The resulting products exhibit efficient hybrid energy storage mechanisms of electric double‐layer capacitance and pseudocapacitance. When the nanosheets are assembled for a symmetric supercapacitor, the device capacitance reaches 107.8 F g⁻¹, at a current density of 0.5 A g⁻¹, and a capacitance retention of 69.6% is achieved at a ten times higher current density of 5 A g⁻¹. Electrochemical impedance spectroscopy reveals that the transition from resistive to capacitive behavior occurs within 0.63 s, indicating that fast ion and charge transport results in high capacitance and rate capability. The corresponding energy and power densities are 9.59 Wh kg⁻¹ and 200.1 W kg⁻¹ at a current density of 0.5 A g⁻¹, demonstrating efficient energy storage in a symmetric supercapacitor.

Herein, unique three-dimensional (3D) hierarchically structured carbon nanofiber (CNF)/metal oxide/conducting polymer composite materials were successfully synthesized by combinations of various experimental methods. Firstly, base CNFs were synthesized by carbonization of electrospun PAN/PVP fibers to attain electric double-layer capacitor (EDLC) characteristics. To further enhance the capacitance, tin oxide (SnO₂) and iron oxide (Fe₂O₃) were coated onto the CNFs via facile hydrothermal treatment. Finally, polypyrrole (PPy) was introduced as the outermost layer by a dispersion polymerization method under static condition to obtain 3D-structured CNF/SnO₂/PPy and CNF/Fe₂O₃/PPy materials. With each synthesis step, the morphology and dimension of materials were transformed, which also added the benign characteristic for supercapacitor application. For the practical application, as-synthesized CNF/SnO₂/PPy and CNF/Fe₂O₃/PPy were applied as active materials for supercapacitor electrodes, and superb specific capacitances of 508.1 and 426.8 F g⁻¹ (at 1 A g⁻¹) were obtained (three-electrode system). Furthermore, an asymmetric supercapacitor (ASC) device was assembled using CNF/SnO₂/PPy as the positive electrode and CNF/Fe₂O₃/PPy as the negative electrode. The resulting CNF/SnO₂/PPy//CNF/Fe₂O₃/PPy device exhibited excellent specific capacitance of 101.2 F g⁻¹ (at 1 A g⁻¹). Notably, the ASC device displayed a long-term cyclability (at 2000 cycles) with a retention rate of 81.1%, compared to a CNF/SnO₂//CNF/Fe₂O₃ device of 70.3% without an outermost PPy layer. By introducing the outermost PPy layer, metal oxide detachment from CNFs were prevented to facilitate long-term cyclability of electrodes. Accordingly, this study provides an effective method for manufacturing a high-performance and stable supercapacitor by utilizing unique 3D hierarchical materials, comprised of CNF, metal oxide, and conducting polymer.

Hollow TiO₂ nanoparticles (HNPs) capped with conducting polymers, such as polythiophene (PT), polypyrrole (PPy), and polyaniline (PANI), have been studied to be used as polarizability-tunable electrorheological (ER) fluids. The hollow shape of TiO₂ nanoparticles, achieved by the removal of the SiO₂ template, offers colloidal dispersion stability in silicone oil owing to the high number density. Conducting polymer shells, introduced on the nanoparticle surface using vapor deposition polymerization method, improve the yield stress of the corresponding ER fluids in the order of PANI < PPy < PT. PT-HNPs exhibited the highest yield stress of ca. 94.2 Pa, which is 5.0-, 1.5-, and 9.6-times higher than that of PANI-, PPy-, and bare HNPs, respectively. The improved ER response upon tuning with polymer shells is attributed to the space charge contribution arising from the movement of the charge carriers trapped by the heterogeneous interface. The ER response of studied ER fluids is consistent with the corresponding polarizability results as indicated by the permittivity and electrophoretic mobility measurements. In conclusion, the synergistic effect of hollow nanostructures and conducting polymer capping effectively enhanced the ER performance.

Light detection and ranging (LiDAR) sensors utilize a near-infrared (NIR) laser with a wavelength of 905 nm. However, LiDAR sensors have weakness in detecting black or dark-tone materials with light-absorbing properties. In this study, SiO₂/black TiO₂ core/shell nanoparticles (SBT CSNs) were designed as LiDAR-detectable black materials. The SBT CSNs, with sizes of 140, 170, and 200 nm, were fabricated by a series of Stöber, TTIP sol-gel, and modified NaBH₄ reduction methods. These SBT CSNs are detectable by a LiDAR sensor and, owing to their core/shell structure with intrapores on the shell (ca. 2–6 nm), they can effectively function as both color and NIR-reflective materials. Moreover, the LiDAR-detectable SBT CSNs exhibited high NIR reflectance (28.2 R%) in a monolayer system and true blackness (L* < 20), along with ecofriendliness and hydrophilicity, making them highly suitable for use in autonomous vehicles.