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- MakaleYalnız künye2026Scopus SJRQ2Practical one-step solvothermal synthesis of photoactive lanthanum(III)hydroxide-metaborate composite nanosheets with suitable band gap for optoelectronics
Karaduman, Oktay
Rare earth compounds, including lanthanide hydroxides, have been greatly interested for their promising uses, such as in optoelectronics or photonics, due to their unique electronic and optical transitions properties based on their 4f electron shells. In this work, for the first time new transparent flower-like lanthanum(III)hydroxide (La(OH)3) with borate (LaB3O6) composite nanosheets having a semiconducting band gap suitable for optoelectronics were synthesized by a very simple one-step solvothermal method from a mixture of pure lanthanum oxide and boron without using water or any acidic solvent or surfactant. The practical synthesis was made for two different solvothermal time durations. The synthesized nanocomposites were investigated by XRD, FIB-SEM imaging, EDS, FTIR, UV-vis absorbance, Raman, Ellipsometry, and TG-DTA analyses. The pure precursors lanthanum oxide (La2O3) and boron converted to La(OH)3 and LaB3O6. EDS elemental mapping showed the homogeneous distribution of elements in the nanocomposites. A strong deep-UV absorbance band was detected. The very low reflectance and excellent visible transmittance (exceeding 86% for the sample with a longer solvothermal process time) reaching infrared region were achieved. The direct and indirect band gap energies were estimated by the Tauc plot method for both of the composite samples. Adding boron reduced the literature given direct band gap value (around 4.5-5.5 eV) of pure La(OH)3. DTA and TGA results revealed the steps of mass losses, including decomposition of La(OH)3. FTIR analyses confirmed the presence of the formed compounds. All results showed that the La(OH)3+LaB3O6 nanocomposites can be suitably used in related applications, including electro-optic, photonic, solar cell, catalysts etc.
- MakaleYalnız künye2024Scopus SJRQ1Preparation and characterization of the highly efficient tetraphenylimidazole substituted Phthalocyanine/ZnO composite and investigation of its effect on the photocatalytic degradation of Rhodamine B and 2,4,6-trichlorophenol
Karaoğlu, Kaan; Yüzüak, Gizem Durak; Yüzüak, Ercüment; Turan, Hanife; Akçay, Hakkı Türker
Growing concerns about industrial waste-induced environmental degradation have driven research towards sustainable solutions. Photocatalytic degradation, fueled by light and avoiding harmful chemicals, offers a promising avenue due to its minimal environmental impact. ZnO, TiO₂, and their derivatives are particularly effective and widely studied photocatalysts. This study aims to prepare new composite materials bearing phthalocyanine and investigate the photocatalytic properties on the degradation of Rhodamine B dye and 2,4,6-trichlorophenol (TCP) as the model compounds. In the initial step, ZnO materials were synthesized using the solvothermal method. Subsequently, a novel Zn(II) complex, including peripherally tetra phenyl imidazole substituted phthalocyanine, was successfully prepared. The composite catalysts were prepared from ZnO materials produced with the tetraphenyl imidazole phthalocyanine Zn(II) complex, called TFI-Zn. The were characterized using instrumental techniques. The photocatalytic characteristics of the composite materials developed were further examined under varying quantities of catalyst and Rhodamine B, variable pH conditions, and varying intensities of UV-A light. In addition, the reusability of the catalyst was investigated. With the new composite photocatalyst prepared within the scope of this study, 98% degradation efficiency and 8.0 × 10−4 min−1 degradation rate was obtained on Rhodamine B solution in 40 min. The newly developed photocatalyst displayed remarkable catalytic activity that remained virtually unchanged for five consecutive cycles, indicating excellent reusability and operational stability. The photocatalytic degradation performance of ZnO-TFI-Zn (1) was also examined on TCP and 90% degradation activity was obtained at the end of 80 min.
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