Mekprasart, Wanichaya
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Mekprasart, Wanichaya
Alternative Name
MEKPRASART, Wanichaya
Mekprasart, W.
Main Affiliation
Email
wanichaya.me@kmitl.ac.th
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Item type:Publication, Structural and photocatalytic properties and X-ray absorption spectroscopic study of BiVO4 nanoparticles incorporated with Fe synthesized by sonochemical method(2022-11-01) ;Wechprasit, Tirapat ;Bootchanont, Atipong ;Sailuam, Wutthigrai ;Wattanawikkam, ChakkaphanKansaard, ThanaphonIn this work, Fe-incorporated BiVO<inf>4</inf> nanoparticles with different Fe-loading contents (0–4%) were synthesized via one-step sonochemical process. Crystal structure of all samples was investigated by X-ray diffraction technique (XRD). XRD patterns obviously show the main structure of monoclinic BiVO<inf>4</inf> structure. The secondary phase is found in the form of Fe-based oxide as a hematite Fe<inf>2</inf>O<inf>3</inf> phase at for Fe-loading contents ≥ 2%. Relevant chemical bonding of as-synthesized samples was carried out by Raman spectroscopy indicating the fundamental vibration with various vibration modes of VO<inf>4</inf><sup>3−</sup> tetrahedron and V–O band, respectively. Morphological structure of pure BiVO<inf>4</inf> shows rod-like structure while 1–4%Fe-incorporated BiVO<inf>4</inf> display different morphologies. The chemical compositions and oxidation numbers of all elements of the samples were carried out via X-ray photoelectron spectroscopy (XPS). XPS spectra indicate the existence of all elements on their surface and the oxidation states of all elements are clearly scrutinized. Local structure of all samples was investigated to interrogate the local atomic site of Fe atoms by X-ray absorption spectroscopy (XAS). The normalized Fe K-edge XANES spectra of all samples indicate that the local atomic site of Fe atoms would not replace in local sites of either Bi or V sites in BiVO<inf>4</inf> crystal verified by simulated XANES spectra. However, the specific features of measured XANES spectra of all samples corresponds to the Fe K-edge XANES spectra of Fe<inf>2</inf>O<inf>3</inf> and BiFeO<inf>3</inf> structure suggesting that local structure of all samples are formed to Fe-based oxide between Fe<inf>2</inf>O<inf>3</inf> and BiFeO<inf>3</inf> structure. Fitting EXAFS spectra of 1–4%Fe-incorporated were practically conducted by artemis program with Fe<inf>2</inf>O<inf>3</inf> and BiFeO<inf>3</inf> used as structural models to identify local atomic environment of Fe atoms. Results show agreeable fitting with their structural models and reveal pertinent information of localization of Fe atoms. Optical properties of the samples were analyzed by UV–Vis diffuse reflectance spectroscopy (UV–Vis DRS). DRS results exhibit the absorption edge in visible range of all samples. Meanwhile, influence of Fe loading contents into pure BiVO<inf>4</inf> displays to confirm the red-shift on the absorption edge in visible range to higher wavelength, which suggests the lower optical band gap of pure BiVO<inf>4</inf>. The optimized photocatalytic degradation of RhB was performed by 4%Fe–BiVO<inf>4</inf> with 82% decolorization under visible-light irradiation within 10 min and exhibited rate constant at 0.150 min<sup>−1</sup>. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Sonochemical synthesis, characterization, and infrared-driven photocatalytic performance of 2%Er/x%Yb co-doped BiVO4 nanoparticles (x=2–10%)(2024-11-01) ;Kansaard, Thanaphon ;Noinonmueng, Tanisara; ;Boondok, DungcharoenWechprasit, TirapatThis study investigates the influence of Yb co-doping on the photocatalytic performance of 2% Er-doped BiVO<inf>4</inf> nanoparticles under infrared light for wastewater treatment. Er/Yb co-doping induces a phase transformation from monoclinic to tetragonal BiVO<inf>4</inf>, significantly enhancing infrared light absorption and photocatalytic activity. The optimal Yb concentration for maximizing activity is found to be 2%, achieving a one-order-of-magnitude improvement compared to undoped BiVO<inf>4</inf>. Up-conversion processes involving Yb and Er ions play a crucial role in this enhancement, converting low-energy infrared photons into higher-energy visible emissions that drive photocatalysis. These findings demonstrate a promising strategy for developing highly efficient and sustainable photocatalysts for wastewater treatment utilizing the abundant yet underexplored infrared region of the solar spectrum.
