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Ashina, C., Pugazhenthiran, N., Sathishkumar, P., Selvaraj, M., Assiri, M. A., Rajasekaran, C., et al. (2023). Ultra-small Ni@NiFe2O4/TiO2 magnetic nanocomposites activated peroxymonosulphate for solar light-driven photocatalytic mineralization of Simazine. J. Environ. Chem. Eng., 11(6), 111342.
Abstract: In the heterogeneous photocatalytic degradation of environmental contaminants the recovery, reuse of employed nanocatalyst was crucial and it is essentially required for the scale up applications. Besides, designing a magnetic material with heterojunction that can effectively oxidize the toxic organic contaminants to non-toxic substance under different reaction conditions including direct solar light irradiation remains a challenge. Considering the above facts, herein, we tailored heterojunction between the magnetic materials and non-magnetic materials with ultra-small Ni nanoparticles modified NiFe2O4/TiO2 nanostructures (Ni@NiFe2O4/TiO2 magnetic nanocomposites) through a simple sonochemical route. The Raman phonons at similar to 540 cm(-1) consistent to nickel metal nanoparticles and the spinel ferrites crystal structure confirmed the formation of Ni@NiFe2O4/TiO2 magnetic nanocomposites. The reduced optical bandgap of the resulting nanocomposites indicated the effective absorption of direct solar light irradiation when compared to the bare TiO2. Thus in-turn, enhanced the photocatalytic efficiency of simazine degradation in the presence of Ni@NiFe2O4/TiO2 magnetic nanocomposites (k= 11.0 x 10(-4) s(-1)) and augmented the activation of peroxymonosulphate (PMS) in the presence of Ni@NiFe2O4/TiO2 magnetic nanocomposites (k= 32.5 x 10(-4) s(-1)). Ni@NiFe2O4/TiO2 +PMS exhibited 3 folds enhanced efficiency in the presence of sunlight. The as-prepared NiFe2O4/TiO2 magnetic nanocatalysts were more stable and the efficiency of simazine oxidation was approximately same for the continuous five cycles at the optimized experimental conditions. The Ni@NiFe2O4/TiO2 magnetic nanocomposites preparation and the activation of PMS may promise the applications in an efficient wastewater treatment.
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Pandiyarajan, T., Mangalaraja, R. V., Karthikeyan, B., Arulraj, A., & Gracia-Pinilla, M. A. (2023). Fabrication and spectroscopic investigation of sandwich-like ZnO:rGO:ZnO: rGO:ZnO structure by layer-by-layer approach. Inorg. Chem. Commun., 149, 110383.
Abstract: Transparent conducting materials (TCMs) are the heart of modern optoelectronic industries and the properties of TCMs could be improved by the introduction of 2D carbon materials. In this report, the influence of order layering on microstructural, transparency and emission characteristics of ZnO:rGO:ZnO:rGO:ZnO and rGO:ZnO: rGO:ZnO:rGO sandwich structures has been investigated. The layer-by-layer approach has been adopted for the fabrication of sandwich structured materials ZnO:rGO:ZnO:rGO:ZnO and rGO:ZnO:rGO:ZnO:rGO through the spin coating technique. The sandwich structures of ZnO and rGO exhibited hexagonal wurtzite structure of ZnO without any impurities were identified through XRD. The ordering of layer's influenced the microstructural parameters and were significantly altered. The spherical nature of the particles and the formation of the sand-wich structures were confirmed by using SEM micrograph. The reduction in an optical transparency and nar-rowing bandgap of the ZnO upon the order of layering were identified through transmission spectra. The lower energy shift of near band edge (NBE) emission and reduction in the emission intensity with respect to pure ZnO nanostructures was observed. The present work provides a simple layer-by-layer approach to fabricating sand-wich structures and improving the optical properties which have potential applications in various optoelectronic devices.
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Sahlevani, S. F., Pandiyarajan, T., Arulraj, A., Valdes, H., Sanhueza, F., Contreras, D., et al. (2024). Tailored engineering of rod-shaped core@shell ZnO@CeO2 nanostructures as an optical stimuli-responsive in sunscreen cream. Mater. Today Commun., 38, 107959.
Abstract: The catalytic efficiency of the materials can be boosted with the selective designing (nanostructures) including the core@shell which aids in attaining the separation of photoinduced charge carriers. However, to effectively separate the carriers and reduce the rate of recombination, tuning the thickness of the shell wall is a vital one. The one-dimensional (1D) rod-like shell wall-controlled ZnO@CeO2 core@shell structures were successfully prepared via co-precipitation and hydrothermal methods using the hexamethylenetetramine (HMTA) as a reagent. The CeO2 shell wall thickness was fine-tuned between 15 and 70 nm with a variation in the concentration of HMTA reagent. The results revealed that the concentration of HMTA played a significant role in the formation of ZnO@CeO2 core@shell structures and in tuning their thickness. The FE-SEM images evidenced the core-shell structures formation with the specific thickness and uniformity. The HR-TEM images confirmed the homogeneity and regular form of the shell thickness. The unit cell and crystallite size were identified from the XRD analysis. The constructed core-shell structures were further employed in the formula of the prototypes of sunscreen and their photoprotective performance was analyzed in the view to cut the solar light irradiation in a new sunscreen formulation. The developed core-shell ZnO@CeO2 structures showed the excellent optical absorption in both the UV as well as visible regions.
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Shanmugaraj, K., Mangalaraja, R. V., Campos, C. H., Singh, D. P., Aepuru, R., Thirumurugan, A., et al. (2023). Gold nanoparticles decorated two-dimensional TiO2 nanosheets as effective catalyst for nitroarenes and rhodamine B dye reduction in batch and continuous flow methods. Inorg. Chem. Commun., 149, 110406.
Abstract: Our environment is greatly endangered by the accumulation of various toxic organic pollutants that are continually produced through unavoidable human needs and the industrialization process. Herein, we report highly active gold nanoparticles (AuNPs) immobilized on two-dimensional (2D) TiO2 nanosheets (AuNPs-TiO2NSs) as a catalyst for the catalytic reduction of nitroarenes (NAs) such as 4-nitroaniline (4-NA), 4-(4-nitrophenyl)morpholine (4-NM), 4-(2-fluoro-4-nitrophenyl)morpholine (4-FNM) and rhodamine B (RhB) dye in the presence of sodium borohydride (NaBH4) medium. Initially, TiO2NSs are prepared by the hydrothermal treatment followed by the modification with 3-aminopropyl-trimethoxysilane (APTMS) coupling agent for strong anchoring of the AuNPs. HR-TEM images exhibit that AuNPs (2.30 +/- 0.06 nm) are immobilized on the surface of ultrathin 2-dimensional TiO2NSs. AuNPs-TiO2NSs catalyst shows excellent catalytic activity towards the reduction of various NAs (4-NA, 4-NM and 4-FNM) and RhB dye with maximum conversion efficiency of >98 %. Moreover, the pseudo-first-order rate constants are estimated as 5.50 x 10- 3 s- 1, 7.20 x 10- 3 s- 1, 6.40 x 10-3 s- 1 and 4.30 x 10-3 s- 1 for the reduction of 4-NA, 4-NM, 4-FNM, and RhB, respectively. For large-scale in-dustrial applications, AuNPs-TiO2NSs catalyst embedded in a continuous flow-fixed bed reactor for the catalytic reduction of 4-NA and RhB dye under optimized reaction conditions. AuNPs-TiO2NSs catalyst shows high con-version rates for 4-NA (>99 %) and RhB (>99%) along with excellent recyclability over 12 cycles in continuous flow fixed bed reactor. The mechanism of synthetic pathway and catalytic reduction of NAs and RhB dye over AuNPs-TiO2NSs catalyst are also proposed. This study may lead to the use AuNPs-TiO2NSs catalyst with superior recyclable catalytic efficiency in various catalytic reactions.
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