A template-free precipitation method was used as a simple and low cost method for preparation of CeO₂ nanoparticles. The structure and morphology of the prepared nanoparticle samples were studied in detail using X-ray diffraction, Raman spectroscopy and Scanning Electron Microscopy (SEM) measurements. The whole powder pattern modelling (WPPM) method was applied on XRD data to accurately measure the crystalline domain size and their size distribution. The average crystalline domain diameter was found to be 5.2 nm, with a very narrow size distribution. UV-visible absorbance spectrum was used to calculate the optical energy band gap of the prepared CeO₂ nanoparticles. The FT-IR spectrum of prepared CeO₂ nanoparticles showed absorption bands at 400 cm^-1 to 450 cm^-1 regime, which correspond to CeO₂ stretching vibration. The dielectric constant (ε_r) and dielectric loss (tan δ) values of sintered CeO₂ compact consolidated from prepared nanoparticles were measured at different temperatures in the range from 298 K (room temperature) to 623 K, and at different frequencies from 1 kHz to 1 MHz.

In this paper a template-free precipitation method was used as an easy and low cost way to synthesize Ag2S semiconductor nanoparticles. The Kramers–Kronig method (K–K) and classical dispersion theory was applied to calculate the optical constants of the prepared samples, such as the reflective index n(ω) and dielectric constant ε(ω) in Far-infrared regime. Nanocrystalline Ag2S was synthesized by a wet chemical precipitation method. Ag2S nanoparticle was characterized by X-ray diffraction, Scanning Electron Microscopy, UV-visible, and FT-IR spectrometry. The refinement of the monoclinic β-Ag2S phase yielded a structure solution similar to the structure reported by Sadanaga and Sueno. The band gap of Ag2S nanoparticles is around 0.96 eV, which is in good agreement with previous reports for the band gap energy of Ag2S nanoparticles (0.9–1.1 eV). The crystallite size of the synthesized particles was obtained by Hall-Williamson plot for the synthesized Ag2S nanoparticles and it was found to be 217 nm. The Far-infrared optical constants of the prepared Ag2S semiconductor nanoparticles were evaluated by means of FTIR transmittance spectra data and K–K method.

The use of graphene and its derivatives with excellent characteristics such as good electrical and mechanical properties and large specific surface area has gained the attention of researchers. Recently, novel nanocomposite materials based on graphene and conducting polymers including polyaniline (PANi), polypyrrole (PPy), poly (3,4 ethyldioxythiophene) (PEDOT), polythiophene (PTh), and their derivatives have been widely used as active materials in gas sensing due to their unique electrical conductivity, redox property, and good operation at room temperature. Mixing these two materials exhibited better sensing performance compared to pure graphene and conductive polymers. This may be attributed to the large specific surface area of the nanocomposites, and also the synergistic effect between graphene and conducting polymers. A variety of graphene and conducting polymer nanocomposite preparation methods such as in situ polymerization, electropolymerization, solution mixing, self-assembly approach, etc. have been reported and utilization of these nanocomposites as sensing materials has been proven effective in improving the performance of gas sensors. Review of the recent research efforts and developments in the fabrication and application of graphene and conducting polymer nanocomposites for gas sensing is the aim of this review paper.

Ternary nanocomposites synergistically combine the material characteristics of three materials, altering the desired charge storage properties such as electrical conductivity, redox states, and surface area. Therefore, to improve the energy synergistic of SnO₂, TiO₂, and three-dimensional graphene, herein, we report a facile hydrothermal technique to synthesize a ternary nanocomposite of three-dimensional graphene-tin oxide-titanium dioxide (3DG-SnO₂-TiO₂). The synthesized ternary nanocomposite was characterized using material characterization techniques such as XRD, Raman spectroscopy, FTIR spectroscopy, FESEM, and EDXS. The surface area and porosity of the material were studied using Brunauer-Emmett-Teller (BET) studies. XRD studies showed the crystalline nature of the characteristic peaks of the individual materials, and FESEM studies revealed the deposition of SnO₂-TiO₂ on 3DG. The BET results show that incorporating 3DG into the SnO₂-TiO₂ binary nanocomposite increased its surface area compared to the binary composite. A three-electrode system compared the electrochemical performances of both the binary and ternary composites as a battery-type supercapacitor electrode in different molar KOH (1, 3, and 6 M) electrolytes. It was determined that the ternary nanocomposite electrode in 6 M KOH delivered a maximum specific capacitance of 232.7 C g^-1 at 1 A g^-1. An asymmetric supercapacitor (ASC) was fabricated based on 3DG-SnO₂-TiO₂ as a positive electrode and commercial activated carbon as a negative electrode (3DG-SnO₂-TiO₂//AC). The ASC delivered a maximum energy density of 28.6 Wh kg^-1 at a power density of 367.7 W kg^-1. Furthermore, the device delivered a superior cycling stability of ∼97% after 5000 cycles, showing its prospects as a commercial ASC electrode.