Thermal decomposition of layered zinc hydroxides (LZHs) is a simple and convenient way to achieve porous ZnO nanostructures. The type of anion contained in an LZH determines the fundamental characteristics of the LZH and thus affects the formation process of the resulting porous ZnO. Here we report a comparative study on the crystal orientation relationship between LZH precursors and the corresponding porous ZnO products by using well-faceted and highly oriented LZH crystals with three different anions, i.e., NO, SO, and Cl. Highly oriented LZH crystals were prepared on layer-by-layer coated indium tin oxide substrates by electrodeposition in aqueous solution and were transformed into porous ZnO by calcination in air. The synthesized materials were characterized by X-ray diffraction, scanning electron microscopy with electron backscatter diffraction, Fourier transformed infrared spectroscopy, and X-ray photoelectron spectroscopy. The layered structure of the highly oriented LZHs was parallel to the substrate surface and all transformed to nanoporous ZnO with a ⟨0001⟩ preferred orientation. The ⟨0001⟩ orientation degree and in-plane orientation of the nanoporous ZnO differed significantly depending on the type of anion but not the decomposition temperature, revealing that the initial formation process of ZnO from the LZHs is crucial. Finally, a possible transformation mechanism explaining the difference in the resulting ZnO orientation by anions (NO, SO, and Cl) is discussed on the basis of their layered structure and thermal decomposition processes.
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http://dx.doi.org/10.1021/acs.inorgchem.8b01242 | DOI Listing |
J Sep Sci
January 2025
Herbal and Traditional Medicines Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic compounds resulting from incomplete burning of organic materials. This work describes the successful layer-by-layer fabrication of a novel zinc oxide nanocomposite made of zinc oxide nanoparticles, aniline, sodium dodecyl sulfate, and modified multi-walled carbon nanotubes on a stainless steel wire by electrodeposition. The coating and extraction conditions were screened, optimized, and validated using factorial design and central composite design, respectively.
View Article and Find Full Text PDFChempluschem
January 2025
Universita degli Studi Di Cagliari, Chemical and Geological Science, S.S. 554 bivio per Sestu, 09042, Monserrato, ITALY.
This work deals with the design of nanocomposite hydrogenation-dehydration bifunctional catalysts for the one-pot conversion of CO2 to dimethyl ether (DME), focusing on obtaining a high and homogeneous dispersion of a Cu-based CO2 hydrogenation phase into the pores of mesostructured supports. Particularly, three aluminosilicate mesostructured acid catalysts with catalytic activity towards methanol dehydration and featuring different porous structures (Al-MCM-41, Al-SBA-15, Al-SBA-16) were synthesized and used as supports to host a CuO/ZnO/ZrO2 (CZZ) CO2 hydrogenation catalyst for methanol synthesis. The use of a mesostructured support allows to maximize the exposed surface of the CO2 reduction function by nanostructuring it through its confinement within the mesochannels, thus obtaining nanocomposite bifunctional catalysts with an ultra-small hydrogenation nanophase.
View Article and Find Full Text PDFRSC Adv
January 2025
Institute of Sciences and Technology, TNU-University of Sciences Thai Nguyen 250000 Vietnam
The sonochemical synthesis of a chitosan-ZnO/FeO nanocomposite yielded a highly porous structure and large surface area for enhancing the photocatalytic degradation of cationic (rhodamine B, RhB) and anionic (methyl orange, MO) dyes in aqueous solution. Chitosan-ZnO/FeO demonstrated a significant enhancement in photodegradation efficiency 99.49% for MO ( = 5.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
P.G. and Research Department of Chemistry, C. Abdul Hakeem College (Autonomous), (Affiliated to Thiruvalluvar University) Melvisharam, Tamil Nadu, India.
This study presents an eco-friendly strategy by developing alginate based photocatalyst, where heterojunction photocatalyst is reinforced in calcium alginate via a facile method called ionotropic gelation. The prepared heterojunction photocatalyst (ZnO-g-CN) and alginate reinforced heterojunction photocatalyst (Alg/ZnO-g-CN) were characterized with Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Thermogravimetric analysis (TGA), UV-visible diffuse reflectance spectroscopy (UV-vis DRS), Field emission scanning electron microscopy (FE-SEM) and X-ray photoelectron spectroscopy (XPS) spectroscopy to confirm their structural, elemental and physicochemical properties. The photodegradation experiments demonstrated Alg/ZnO-g-CN showed excellent efficiency in the removal of methylene blue (MB) under both UV-vis light and natural sunlight irradiation.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Physics, National Institute of Technology Nagaland, Chumukedima, Dimapur 797103, India.
An exceedingly porous and interwoven fibrous structure was achieved in this study by interlocking titanium carbide (TiC) MXenes onto the electrospun mats using poly(vinylidene fluoride) (PVDF) as the base polymer. The fibrous membrane was further modified with the inclusion of zinc oxide (ZnO) and tungstite (WO·HO) nano/microstructures via annealing and hydrothermal approaches. Through these strategic interfaced morphological developments in novel TiC/ZnO/WO·HO heterostructures, our findings reveal enhanced wettability and charge-segregation desirable for promoting oil-water separation and photoreactivity, respectively.
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