The invention of carbon and its allotropes have transformed the electronic and optoelectronic industry due to their encouraging properties in a large spectrum of applications. The interesting characteristic of carbon is its ability to form many allotropes due to its valency. In recent decades, various allotropes and forms of carbon have been invented, including fullerenes, carbon nanotubes (CNTs), and graphene (GR). Since the inception of nanotechnology, carbon allotropes-based nanocomposites have become a leading sector of research and advancement due to their unique bonding properties. Fullerenes and CNTs-based polymer nanocomposites have attracted significant research interest due to their vast applications in every sphere of science and technology. Current research impetus reveals that carbon and its allotropes have revolutionized the industry and academia due to their fascinated properties. Recent advances in various aspects of graphene, CNTs, graphene nanoribbons, fullerenes, carbon encapsulates, and their nanocomposites with polymeric materials and their different applications are reported in this review article. Also, current status and future prospects of graphene-based polymer nanocomposites are presented in common along with proper citations extracted from the scientific literature. Moreover, this article is a unique collection of vital information about GR, CNTs, fullerenes, and graphene-based polymer nanocomposites in a single platform.

This paper reports on the defect correlated self-quenching and spectroscopic investigation of calcium titanate (CaTiO₃) phosphors. A series of CaTiO₃ phosphors doped with trivalent europium (Eu³⁺) and codoped with potassium (K⁺) ions were prepared by the solid state reaction method. The X-ray diffraction results revealed that the obtained powder phosphors consisted out of a single-phase orthorhombic structure and it also indicated that the incorporation of the dopants/co-dopants did not affect the crystal structure. The scanning electron microscopy images revealed the irregular morphology of the prepared phosphors consisting out of μm sized diameter particles. The Eu³⁺ doped phosphors illuminated with ultraviolet light showed the characteristic red luminescence corresponding to the ⁵D₀→⁷F_J transitions of Eu³⁺. As a charge compensator, K⁺ ions were incorporated into the CaTiO₃:Eu³⁺ phosphors, which enhanced the photoluminescence (PL) intensities depending on the doping concentration of K⁺. The concentration quenching of Eu³⁺ in this host is discussed in the light of ion-ion interaction, electron phonon coupling, and defect to ion energy transfer. The spectral characteristics and the Eu-O ligand behaviour were determined using the Judd-Ofelt theory from the PL spectra instead of the absorption spectra. The CIE (International Commission on Illumination) parameters were calculated using spectral energy distribution functions and McCamy's empirical formula. Photometric characterization indicated the suitability of K⁺ compensated the CaTiO₃:Eu³⁺ phosphor for pure red emission in light-emitting diode applications.

Heavy metal is released from many industries into water. Before the industrial wastewater is discharged, the contamination level should be reduced to meet the recommended level as prescribed by the local laws of a country. They may be poisonous or cancerous in origin. Their presence does not only damage people, but also animals and vegetation because of their mobility, toxicity, and non-biodegradability into aquatic ecosystems. The review comprehensively discusses the progress made by various adsorbents such as natural materials, synthetic, agricultural, biopolymers, and commercial for extraction of the metal ions such as Ni²⁺, Cu²⁺, Pb²⁺, Cd²⁺, As²⁺ and Zn²⁺ along with their adsorption mechanisms. The adsorption isotherm indicates the relation between the amount adsorbed by the adsorbent and the concentration. The Freundlich isotherm explains the effective physical adsorption of the solute particle from the solution on the adsorbent and Langmuir isotherm gives an idea about the effect of various factors on the adsorption process. The adsorption kinetics data provide valuable insights into the reaction pathways, the mechanism of the sorption reaction, and solute uptake. The pseudo-first-order and pseudo-second-order models were applied to describe the sorption kinetics. The presented information can be used for the development of bio-based water treatment strategies.

This paper reports on the structural, optical and photometric characterization of an Eu³⁺/Dy³⁺ doped yttrium oxysulfide phosphor (Y₂O₂S:Eu³⁺/Dy³⁺) for near white emission in solid state lighting.

This review attempts to compile the physics and chemistry of defects in zinc oxide (ZnO), at both, the fundamental and application levels. The defects, either inherent ones or introduced externally, have broadened the ZnO material field in various directions. The ZnO material exhibits many defect-attributed properties leading to broad technological applications: electronic and optoelectronic devices, sensors, optical components, ceramic industry, biomedical, catalysis, lightening, etc . Considering the huge defect-dependent technological scopes, the ZnO material is constantly engineered for various defects, and corresponding functionalities are tailored with respect to particular applications. The functional properties of ZnO are strongly influenced by the defects, and as a result, the defect engineering of the ZnO materials has remained an important motivation in materials science and engineering in terms of localized defects, extended defects, impurities, and surface defects, etc . A detailed characterization of these defects seems to be an essential part of any research area. The correlations of the microstructural characteristics with electrical and optical properties of ZnO are then a natural step for further facilitating an efficient way toward advanced ZnO-based materials and devices. The present review is an effort to shed light on the defects of ZnO, properties, theoretical aspects, and corresponding applications.