The controlled chemical oxidative polymerization of metanilic anion $(m{\text{-NH}}_2{\text{C}}_6{\text{H}}_4{\text{SO}}_3^{-})$$(m{\rm{ - N}}{{\rm{H}}_2}{{\rm{C}}_6}{{\rm{H}}_4}{\rm{SO}}_3^ - )$ within the interlayer of NiAl layered double hydroxide was performed using, for the first time, ammonium persulfate as the oxidizing agent. The quantity of oxidizing agent required for control of the interlayer polymerization was investigated systematically and it was found that interleaved polyaniline sulfonic (PANIS) was present in different oxidation states and protonation levels when different quantities of external oxidizing agents were added. A mechanism for the oxidative polymerization of metanilic anion in NiAl layered double hydroxide is proposed, based on the intercalation of the oxidizing agent and the interlayer polymerization of monomer. The resulting PANIS/NiAl LDH composites were characterized by powder X-ray diffraction, ultraviolet-visible absorption spectra, Fourier transform infrared and X-ray photoelectron spectroscopy.

Wearable electrochromic devices are considered as the essential components for the development of smart clothing with the intelligent sensing, actuating, and displaying functions. In this study, the electrochromic composite flexible membranes of polyaniline (PANI) and reduced graphene oxide (RGO) were fabricated by in situ polymerization of aniline monomer in the presence of RGO dispersion. The effects of RGO concentration on the morphology, chemical structure, crystallinity, and electrochromic behavior of the composite membranes were studied. Our experimental results show that the conductivity of PANI/RGO composite membrane increases with the increasing of RGO concentration from 0.1 to 0.25 wt%, and the highest conductivity is 3.57 S/cm. An improved electrochemical performance with good electrochromic cycle characteristic of the PANI/RGO composite can be obtained, which shows a wide color range from green to black compared with the PANI membrane that ranging from green to dark blue. This research provides a systematical investigation of flexible PANI-based electrochromic membrane, which has the potential application in the field of wearable electrochromic devices in the future.

The present work describes the effect of montmorillonite (MMT) particles on the alignment of conducting polyaniline (PANI) chains in a PANI/MMT composite. The composite was prepared both as a powder, pressed into pellets, and as thin films deposited on glass surfaces. For comparison, pure PANI was also prepared in these two forms. A combination of X-ray powder diffraction analysis and molecular modelling confirmed the successful intercalation of the PANI into theMMT, while Raman spectroscopy confirmed the presence of the conducting form of PANI (i.e. the emeraldine salt) in all samples. Scanning electron microscopy, transmission electron microscopy and atomic force microscopy were used to study the morphologies of all samples. Conductivity measurements showed that the presence of the MMT particles in the PANI/MMT composites contributes to a significant increase in the electrical conductivity in comparison with the pure PANI samples. Moreover, in the pressed pellets the presence of theMMT particles led to an extremely high electrical anisotropy. TheUV-VIS spectroscopy results showed that the PANI/MMT thin film exhibited a selective transmittance in the range 450–650 nm; therefore, the PANI/MMT thin film is not only conductive, but also suitable for use in various optical applications.

Developing high energy density supercapacitors is of great importance to the transportation, consumer electronics, and micro-grid energy storage sectors. Recently, the development of high voltage organic electrolyte based supercapacitor devices has been gaining much attention. Among them, there is an on-going intense interest in investigating high capacity lithium ion storage anode materials in hybrid supercapacitors. However, developing high capacity cathode materials for high voltage organic electrolyte supercapacitor devices is rarely investigated. The low electrical double layer capacitances of carbon cathode electrodes, which are widely used in current supercapacitor devices, are often the limiting bottleneck. In this contribution, we investigated the electrochemical energy storage behavior of a polyaniline (PANI)-single wall carbon nanotube (SWCNT) composite material in an organic electrolyte as a supercapacitor cathode. The PANI-SWCNT composite exhibits a high specific capacitance of 503 F/g, of which 58.8% of the total capacitance is attributed to the pseudocapacitive and electrical double layer energy storage. The cycling stability of the PANI-SWCNT composite could be further improved by polydopamine (PDA) modification. The PDA with strong adhesion properties is able to prevent mechanical degradation. The PDA modified PANI-SWCNT shows excellent stability with only 5% degradation after 2000 cycles.

A facile synthesis method was adapted to prepare Ortho-chloropolyaniline/graphite oxide (OPANI/GO) composites. The properties of these composites have been discussed based on different characterizations such as scanning electron microscopy, FTIR, and dielectric studies. The important peaks of benzenoid and quinoid rings in the spectrum confirm the formation of composites. Scanning electron microscopic studies indicate that the morphology of the prepared composites was influenced by different weight ratios of GO in OPANI and the resulting micrographs of these composites exhibited flaky and folded structures. The electrical conductivity study was carried out and found that 6 wt% of GO in PANI shows high conductivity value of 20 × 10−2 S/cm. The obtained results suggest an easy approach to prepare such novel nanocomposites with excellent dielectric properties which can be used in many technological applications.

By using microemulsion-mediated solvothermal method in the presence of camphorsulfonic acid as a dopant, self-aggregated polyaniline (PANI) nanowires were synthesized and further organized into three-dimensional cluster-connected networks. So-formed PANI exhibited a hierarchically porous structure, which was significantly different from those obtained by conventional chemical oxidation method, hydrothermal method, and other reported methods. Compared with nanofibers presented in this study, the nanowires in the clusters had a great decrease in diameter from ∼60 to ∼15 nm due to the space-confined polymerization. In addition, the size of the clusters could be easily adjusted by altering the dopant/monomer molar ratio. A probable assembly mechanism for such an interesting morphology was proposed. Used as an electrode material, PANI clusters showed high specific capacitances (510 and 368 F g−1 at 0.5 and 2 A g−1, respectively) and improved cycling stability (66% capacitance retention over 1000 cycles) as compared to PANI fibers and particles obtained by other methods, which may be related to its unique morphology and high doping level.