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[Display omitted] • Plasma-based doping of composite materials was an efficient way to reduce the band gap. • Plasma-based doping promoted substitutional doping. • Different methods for plasma discharge for doping were discussed. • Limited studies were performed on the real-life applications of plasma-based materials. • An in-depth understanding of the mechanisms was required for computational modelling. In recent years, solar energy-driven photocatalysis materials have drawn significant attention to addressing the global energy and environmental crisis. However, many of the semiconductor photocatalysts are unable to absorb the visible light of the solar spectra due to their wide band gap. The incorporation of a foreign element such as a dopant in the lattice of these photocatalysts was shown to reduce their band gap and enhance visible light absorption. The doping of semiconductors can be performed using several techniques such as sol–gel, hydrothermal, solvothermal, and plasma-based doping. However, plasma-based doping has been considered a highly efficient approach due to the reduction of the band gap to a large extent, enhancement of visible light absorption, and remarkable photocatalytic activities under visible light illumination. The plasma-based doping approach offered many advantages such as high reactivity, process simplicity, scalability, energy efficiency, homogeneous doping, no chemical inventory, low pressure, and low-temperature operation, and flexibility of operation under gas and liquid phase media. Further advancement of plasma-based doping can be achieved through more theoretical studies allowing an in-depth understanding of the mechanisms and interactions of the species involved. This will facilitate the synthesis and application of doped photocatalysts in a cost-effective manner. This review surveyed recent advances in a wide range of semiconductor photocatalysts doped with various dopants using plasma treatment. Various plasma methods for doping semiconductor photocatalysts and their fundamental mechanisms were discussed. The performance characteristics of the plasma-doped photocatalysts were compared to other methods in terms of energy and environmental applications including degradation of environmental contaminants and solar fuel production such as hydrogen production from water splitting using visible light-driven solar energy. Finally, potential future research directions were recommended for the applications of the efficient photocatalysts developed by plasma treatment. [ABSTRACT FROM AUTHOR]

[Display omitted] • The functional ligand-based conjugate materials were prepared for Eu(III) adsorption. • The materials exhibited high selectivity even in the presence of diverse foreign ions. • A high adsorption capacity (176.31 mg/g) was found in the Langmuir model. The hybrid donor chemical ligand of 5- tert -butyl-2-hydroxybenzaldehyde thiosemicarbazone (THTB) was prepared and then embedded onto inorganic porous silica as hybrid conjugate materials (HCM). The Europium (Eu(III)) ion was selected from the lanthanides (Ln(III)) series for green and robust adsorption and recovery based on the adsorption, complexation, and selectivity tendency from the standpoint of the pH-dependent factor. The chemical compound of THTB consisted of O-, N-, and S-donor atoms and was able to make stable complexation with Ln(III) ions in optimum conditions due to the open functionality of the HCM. A surface complexation with a good complexation fitting to the experimentally collected data was used to describe the adsorption mechanism. The Eu(III) ion adsorption performance was measured with batch equilibrium methods. The affecting experimental protocols including solution pH, contact time, initial Eu(III) ion concentration, foreign ions effect, and recovery were carried out and evaluated consistently. The Eu(III) ion adsorption by the HCM was at pH 5.0 and this pH was selected to avoid the precipitation problem to ensure the adsorption mechanism. The co-existing several metal ions were not interfered with Eu(III) ion adsorption by the HCM due to the high affinity between Eu(III) ion and the functional groups of HCM. The bonding mechanism suggested that O-, N-, and S-donor atoms of THTB were strongly coordinated to Eu(III) with 2:1 ratio complexation. The Langmuir adsorption isotherm model was plotted due to the HCM morphology and applied to validate the adsorption isotherms according to the homogeneous ordered frameworks. The Eu(III) ion adsorption capacity by the HCM was 176.31 mg/g as expected because of the high surface area of the HCM. The adsorbed Eu(III) ion was completely eluted from HCM with the eluent of 0.20 M HNO 3 and simultaneously regenerated into its initial form without significant deterioration. This study could be of great applicative utility for Eu(III) ions from waste aqueous solutions as green technology. [ABSTRACT FROM AUTHOR]