Preparation of mesoporous ThO2 nanoparticles: Influence of calcination on morphology and visible-light-driven photocatalytic degradation of indigo carmine and methylene blue.

The present article reports the synthesis of thoria nanoparticles (ThO2 NPs) via sol-gel process and examines the effect of calcination temperature of ThO2 on the morphology and photocatalytic degradation of indigo carmine (IC) and methylene blue (MB) under visible-light. As-synthesized white crystals of ThO2 were subjected to calcination at different temperatures, viz. 700 °C (TH-700), 800 °C (TH-800), and 900 °C (TH-900). The effect of calcination temperature on the structural, morphological, thermal, surface area-porosity, and optical properties of ThO2 NPs were investigated by diverse analytical techniques. XRD patterns show the cubic-space group Fm-3m (225) with parameter a = 5.597 Å and reveals crystallite sizes increased with calcination temperature. The bandgap energy was found to be 1.85 eV, 2.33 eV, and 2.71 eV for TH-700, TH-800, and TH-900 NPs, respectively, calculated by Kubelka-Munk (KM) plot. SEM and TEM unveil that the sample TH-700 calcined at a low temperature of 700 °C yields assembled nanosheets, while at higher temperatures, i.e., 800 °C (TH-800) and 900 °C (TH-900), produces agglomerated nanomaterials. Further, TH-700 sample exhibits enhanced photocatalytic degradation within 120 min for both IC and MB dye than TH-800 and TH-900 counterparts. Among the dyes, IC shows improved photocatalytic efficiency than MB for TH-700, owing to the increased optical absorption and improved separation of photogenerated charge carriers. The reusability study of TH-700 reveals that the catalysts were stable up to four successive cycles with no drastic changes in photocatalytic efficiency. Also, systematic photodisintegration of IC was investigated by Liquid chromatography-mass spectrometry (LC-MS).

Mesoporous Octahedron-Shaped Tricobalt Tetroxide Nanoparticles for Photocatalytic Degradation of Toxic Dyes.

The present article reports a facile approach to fabrication of mesoporous octahedron-shaped tricobalt tetroxide nanoparticles (Co3O4 NPs) with a very narrow size distribution for eco-friendly remediation of toxic dyes. Co3O4 NPs were fabricated by a sol-gel process using cobalt chloride hexahydrate (CoCl2·6H2O) and monosodium succinate (C4H5O4Na) as a chelating/structure-directing agent and sodium dodecyl sulfate as a surfactant. Moreover, the phase structure, elemental composition, and thermal and morphological facets of Co3O4 NPs were investigated using XRD, FT-IR, EDS, Raman, XPS, TGA, SEM, and TEM techniques. The face-centered cubic spinel crystalline structure of the Co3O4 NPs was confirmed by XRD and SEM, and TEM analysis revealed their octahedron morphology with a smooth surface. Moreover, the narrow pore size distribution and the mesoporous nature of the Co3O4 NPs were confirmed by Brunauer-Emmett-Teller measurements. The photocatalytic activity of Co3O4 NPs for degradation of methyl red (MR), Eriochrome Black-T (EBT), bromophenol blue (BPB), and malachite green (MG) was examined under visible light irradiation, and the kinetics of the dye degradation was pseudo-zero-order with the rate constant in the order of MR > EBT > MG > BPB. Furthermore, the mechanism of photo-disintegration mechanism of the dye was examined by a scavenging test using liquid chromatography-mass chromatography, and its excellent photodegradation activities were attributed to the photogenerated holes (h+), superoxide (O2 -) anions, and hydroxyl (·OH) radicals. Finally, the synergistic effect of the nano-interconnected channels with octahedron geometry, mesoporous nature, and charge transfer properties along with photogenerated charge separations leads to an enhanced Co3O4 photocatalytic activity.

Phytosynthesis of nearly monodisperse CuO nanospheres using Phyllanthus reticulatus/Conyza bonariensis and its antioxidant/antibacterial assays.

In the present article we have developed an eco-friendly, phytosynthetic, cost-effective and straightforward method for the synthesis of nearly monodisperse CuO nanospheres (NSP) using leaf extracts of medicinal plants Phyllanthus reticulatus (PR) and Conyza bonariensis (CB) as novel green reducing agents. Copper nitrate (Cu (NO3)2) was used as a precursor. The stoichiometric ratio of both leaf extracts (PR/CB) and Cu(NO3)2 was standardized for the synthesis of NSP. During formation of CuO NSP, a color of solution gradually changed from light greenish-blue to black with a number of intermediate stages and it correlated to the reduction reaction catalyzed by phytochemicals. As-synthesized materials were characterized in detail at the structural, electronic level and morphological authentication by XRD, FT-IR, EDS, UV-DRS, Raman, XPS, SEM, TEM, BET and AFM. SEM studies of phytosynthesized materials revealed nearly monodisperse nanospheres, while TEM rendered average particles size 4-14 nm. Also, AFM profiles suggested a homogenized nature of the nanospheres. Then, the antioxidant property was obtained by α, α-diphenyl-ß-picrylhydrazyl (DPPH). Ethanolic, methanolic extracts were used for the antioxidant activity, while ascorbic acid was used as a standard medium. Each plant extract exhibited noteworthy antioxidant activity. Moreover, the antibacterial activity of CuO NSP (PR/CB) was tested against human pathogenic bacteria viz. gram-positive Staphylococcus aureus, Klebsiella pneumoniae, and gram-negative Escherichia coli. Result rendered effective antibacterial activity against Escherichia coli.