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Preparation of Ag-AgVO3/g-C3N4 composite photo-catalyst and degradation characteristics of antibiotics
摘要： The degradation of tetracycline by silver vanadate (AgVO3), graphite-like carbon nitride (g-C3N4) and their composites was studied by visible light photocatalysis. Their structures and morphologies were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Their degradation intermediates were analyzed by GC-MS. Nanorod silver vanadate was synthesized by hydrothermal method. The results show that the gap between nanorods is reduced by adding spinning carbon nitride, and the photocatalytic performance of the composite is stronger than that of single material. The reaction rate constants of Ag-AgVO3/g-C3N4 composites were 0.0298 min-1, 2.4 and 2.0 times that of g-C3N4 (K=0.0125 min-1) and AgVO3 (K=0.0152 min-1), respectively. At 120 minutes, the degradation rate of the composites reached 83.6%. The degradation of tetracycline was confirmed by GC-MS, and a possible degradation process was proposed.
关键词： Photo-catalysis,Carbon nitride,Antibiotics,Visible light,Silver vanadate
更新于2025-11-21 10:59:37
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Broad-band emission and color tuning of Eu3+-doped LiCa2SrMgV3O12 phosphors for warm white light-emitting diodes
摘要： In this study, series of Eu3+-doped LiCa2SrMgV3O12 (LCSMV) phosphors with broad-band emission and color tunable feature were prepared via solid phase reaction. The X-ray diffraction (XRD) and scanning electron microscopy (SEM) results presented a pure cubic phase product with micron-sized and homogeneous distribution of element. Their spectroscopic properties were investigated systematically by photoluminescence excitation (PLE) and emission (PL) spectra, temperature-dependent PL spectra and luminescence decay curves. The LCSMV phosphors displayed a strong absorption to ultraviolet light and a broad cyan emission. Moreover, in Eu3+-doped LCSMV phosphors, Eu3+ ion characteristic emissions at 589, 610, 651 and 705 nm, attributing to the 5D0→7F1, 7F2, 7F3 and 7F4 transitions, were observed. Along with Eu3+ ion concentrations increasing, the emission colors could be readily tuned from cyan to orange and the decay lifetimes of (VO4)3- became shorter. Meanwhile, electric dipole-dipole interaction was responsible to energy migration from (VO4)3- groups to Eu3+ ions. Further, the quantum efficiency (QE) values were estimated to be 32.5% for LCSMV host and 39.3% for LCSMV: 0.01Eu3+ sample. Finally, a LED lamp was prepared by integrating the blend of the LCSMV: 0.01Eu3+ phosphors and commercial blue-emitting BaMgAl10O17:Eu2+ phosphors with NUV chip (365 nm) and exhibited warm white light (CCT = 3655 K, Ra = 90), which may be applied in lighting and display field.
关键词： Self-activated luminescence,Color tunable,Light-emitting diode,Vanadate phosphor,Color rendering index,Broad-band emission
更新于2025-11-20 15:33:11
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Synthesis, energy transfer and multicolor luminescent property of Eu3+-doped LiCa2Mg2V3O12 phosphors for warm white light-emitting diodes
摘要： In this study, Eu3+-doped LiCa2Mg2V3O12 (LCMVO) phosphors with multicolor luminescent property were prepared by the solid phase reaction. Their structure, morphology and luminescent property were studied systematically by X-ray diffraction, scanning electron microscope and photoluminescence spectra. The LCMVO phosphors showed pure cubic crystal structure with space group (3Ia d ) and irregular spherical morphology. The excitation spectra showed a strong absorption to ultraviolet light. Under the excitation wavelength at 360 nm, they exhibited a cyan emission with a luminescence center at 520 nm. When Eu3+ ions were doped into LCMVO system, the Eu3+ characteristic emissions were also observed and the emission colors were tuned from cyan to orange via adjusting Eu3+ ion concentration. Further, electric dipole-quadrupole interaction and luminescence decay curves were adopted to explain the energy transfer from (VO4)3- to Eu3+. The emission spectra of as-obtained phosphors at different temperature were measured to evaluate their thermal stability. The quantum efficiency values were measured to be 42.5% for LCMVO host and 38.6% for LCMVO: 0.01Eu3+ sample. The final prepared LED lamp showed easeful warm white light with suitable Ra of 89 and CCT of 3847 K, respectively. These results suggest LCMVO phosphors may be applied in near ultraviolet chip-excited white light-emitting diodes.
关键词： energy transfer,multicolor luminescent,self-activated luminescence,excitation and emission spectra,vanadate phosphor,UV-LED
更新于2025-11-20 15:33:11
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Optical and photocatalytic properties of bismuth vanadate doped bismuth silicate glasses
摘要： The aim of this research is to investigate optical and photocatalytic properties of 0.25, 0.5 and 1.0 mol% BiVO4 doped bismuth silicate glasses. The glasses composition is 60 mol% SiO2 and 40 mol% Bi2O3. Optical spectra and the analysis of color by CIELab system revealed that the addition of BiVO4 changed the color of the glasses from pale yellow to yellow-orange with the narrower band gap. Photocatalytic activity was observed in 0.5 and 1.0 mol% BiVO4-doped glass. The effect of BiVO4 doping to bismuth silicate glass is also discussed.
关键词： Optical,Photocatalysis,Bismuth vanadate,Bismuth silicate glass,CIELab
更新于2025-11-14 15:30:11
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Photoelectrochemical enhancement from deposition of BiVO4 photosensitizer on different thickness layer TiO2 photoanode for water splitting application
摘要： TiO2 is a prominent photocatalyst and has been pioneering the research in water splitting for hydrogen cell production. However, TiO2 has low visible region absorption which limit its functionality as a photoabsorber and requires addition of other high absorptive material such as BiVO4. Fabrication of TiO2 photoanode on FTO substrate and deposition of BiVO4 on TiO2 were done using simple spin coating procedure. TiO2/BiVO4 photoelectrode were first tested for its photo absorption, photocurrent generation and electrical impedance to obtain the optimized sample. Optimized sample then further tested for its photocurrent generation stability using linear sweep voltammetry and time dependent photocurrent test. Photo absorption enhancement from TiO2/BiVO4 of almost 10 folds achieved along the visible region comparing to pure TiO2. Photogenerated charge produced from TiO2/BiVO4 is also 3 folds higher compared to pure TiO2at water oxidation threshold potential at 1.23 V vs. RHE. From photocurrent generation analysis, heterostructure of TiO2/BiVO4 proven to produce more than 3 folds higher photocurrent comparing to both pure TiO2 and BiVO4.
关键词： Z-scheme,Bismuth vanadate,Thin-film,Titanium dioxide,Photoelectrochemical water splitting
更新于2025-11-14 15:19:41
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Visible light driven photoelectrocatalysis on a FTO/BiVO4/BiOI anode for water treatment involving emerging pharmaceutical pollutants
摘要： Contamination of water bodies by harmful and recalcitrant organic substances is a global challenge. A promising technique for removing these organics from water/wastewater is photoelectrocatalytic oxidation which combines electrolytic and photocatalytic processes. Herein, we report the degradation of emerging pharmaceutical pollutants e acetaminophen and cipro?oxacin e at a BiVO4/BiOI photoanode under visible irradiation via photoelectrocatalytic process. The BiVO4/BiOI was electrodeposited on a FTO glass and characterised with XRD, SEM, EDS and diffusive re?ectance UVeVis. The results con?rmed the successful electrodeposition of BiVO4/BiOI on the glass substrate. Mott-Schotty plots con?rmed the formation of p-n heterojunction between the two electrodeposited semiconductors. The calculated charge carrier density of BiVO4/BiOI was higher than those of pristine BiVO4 and BiOI. The binary electrode also gave improved photocurrent response compared with unitary electrodes. Degradation ef?ciencies of 68% and 62% were achieved upon the application of the prepared photoanode (FTO/BiVO4/BiOI) in PEC degradation of acetaminophen and cipro?oxacin respectively using a bias potential of 1.5 V within 2 h. A synthetic pharmaceutical wastewater containing a mixture acetaminophen and cipro?oxacin was also treated with the photoanode. The photoanode was also effective in the degradation of dye. The ?ndings of this study suggest the suitability of the prepared photoanode for the photoelectrocatalytic degradation of organic pharmaceutical pollutants in wastewater.
关键词： Cipro?oxacin,p-n heterojunction photoanode,Photoelectrocatalytic degradation,Bismuth oxyiodide,Acetaminophen,Bismuth vanadate
更新于2025-11-14 14:48:53
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High Temperature One-Step Synthesis of Efficient Nanostructured BiVO4 Photoanodes for Water Oxidation
摘要： Bismuth vanadate (BiVO4) is a promising photoanode material for photoelectrochemical water splitting due to its well-suited valence band edge and comparatively narrow band gap. Herein, we provide first insights on the high temperature rapid and scalable synthesis of efficient nanostructured BiVO4 photoanodes for water oxidation. Nanostructured BiVO4 films with tunable optical density and porosity from 12 to 80% have been synthesized in few seconds by direct deposition of flame-made BiVO4 nanoparticle aerosols. The impact of BiVO4 film structural properties on the photooxidation performance has been systematically investigated by a set of electrochemical and physical characterizations indicating key directions for its morphological optimization. It was found that the BiVO4 water oxidization performance is mainly determined by two competitive factors, viz. accessible surface area and carrier conductivity through the grain boundaries. Optimization of these two factors increased the photocurrent densities by more than 3 times resulting in ca 1.5 mA cm-2 for sulphite oxidation and ca 1 mA cm-2 for water oxidation with a FeOOH\NiOOH co-catalyst at 1.0 V vs. the reversible hydrogen electrode (VRHE) under simulated one sun illumination. These findings provide novel insights into the structure-activity relationships of high temperature synthesized BiVO4 photoanodes for solar-powered water splitting, and introduce a scalable and low-cost approach for their rapid nanofabrication.
关键词： Flame Synthesis,Bismuth Vanadate,Scalable,One-Step,Photoelectrochemical Water Splitting
更新于2025-10-22 19:40:53
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A novel Z-scheme Ag3VO4/BiVO4 heterojunction photocatalyst: Study on the excellent photocatalytic performance and photocatalytic mechanism
摘要： A novel three-dimensional microspheres mediator-free Z-scheme Ag3VO4/BiVO4 heterojunction photocatalyst was successfully obtained for the first time. The photocatalytic performance of the as-prepared photocatalyst was systematically examined via the photocatalytic reduction of Cr6+ and oxidation of Bisphenol S under visible-light irradiation. Among these samples, 0.24-Ag3VO4/BiVO4 exhibits the highest photocatalytic performances, the photocatalytic reduction and oxidation efficiency of 74.9 and 94.8 %, respectively, can be achieved. The enhanced photocatalytic performance is attributed to the build-in electric field assisted charge transfer between the Ag3VO4 and BiVO4, and the increasing lifetime of the charge carrier confirmed by the results of time-resolved fluorescence spectra and photoelectrochemical measures. Moreover, based on the results of free radical scavenging activity test, and EPR experiments, it has been verified that the Ag3VO4/BiVO4 heterostructures follow a typical Z-scheme charge transfer mechanism rather than conventional type-II heterojunction charge transfer mechanism. Furthermore, the theoretical understanding of the underlying mechanism was also supported, while the energy band structure, and Fermi level were systematically calculated using the density functional theory approach. The results show that a built-in electric field directed from Ag3VO4 to BiVO4 surface was established as an equalized Fermi level was reached, which benefits the separation of photogenerated charge carriers in the way of a Z-scheme charge transfer mechanism. The strategy to form the three-dimensional microspheres Z-scheme heterojunction photocatalyst may offer new insight into the Z-scheme charge transfer mechanism for applications in the field of solar energy conversion.
关键词： Bismuth Vanadate,Z-scheme heterojunction photocatalyst,photocatalytic reduction and oxidation.
更新于2025-09-23 15:23:52
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Aging of a Vanadium Precursor Solution: Influencing Material Properties and Photoelectrochemical Water Oxidation Performance of Solution-Processed BiVO <sub/>4</sub> Photoanodes
摘要： Metal–organic decomposition is an easy way to fabricate BiVO4 (BVO) photoanodes; however, it often experiences a reproducibility issue. Here, the aging duration of a vanadium precursor solution, vanadyl acetylacetonate in methanol, is identified as a factor that profoundly affects reproducibility. Substantial changes in structural, optical, and electrical properties of BVO films are observed upon varying aging time of vanadium precursor solutions, which subsequently impacts photoelectrochemical (PEC) water oxidation and sulfite oxidation reactions. With the optimum number of aging days (3 d), some deficiency of oxygen is observed, which is accompanied by an increase in carrier concentration and a reduced charge transfer resistance in the PEC device, which produces the highest PEC performance that is comparable to the state-of-the-art undoped BVO photoanodes. The findings point to the importance of understanding solution chemistry and demonstrate that utilization of the understanding of fine adjustment of the composition of BVO films can produce highly reproducible and efficient BiVO4 photoanodes.
关键词： solution aging,metal–organic decomposition,bismuth vanadate,chemical composition,photoelectrochemical water splitting
更新于2025-09-23 15:23:52
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Manipulation of Charge Transport by Metallic V <sub/>13</sub> O <sub/>16</sub> Decorated on Bismuth Vanadate Photoelectrochemical Catalyst
摘要： Conductive metal oxides represent a new category of functional material with vital importance for many modern applications. The present work introduces a new conductive metal oxide V13O16, which is synthesized via a simplified photoelectrochemical procedure and decorated onto the semiconducting photocatalyst BiVO4 in controlled mass percentages ranging from 25% to 37%. Owing to its excellent conductivity and good compatibility with oxide materials, the metallic V13O16-decorated BiVO4 hybrid catalyst shows a high photocurrent density of 2.2 ± 0.2 mA cm?2 at 1.23 V versus reversible hydrogen electrode (RHE). Both experimental characterization and density functional theory calculations indicate that the superior photocurrent derives from enhanced charge separation and transfer, resulting from ohmic contact at the interface of mixed phases and superior electrical conductivity from V13O16. A Co–Pi coating on BiVO4–V13O16 further increases the photocurrent to 5.0 ± 0.5 mA cm?2 at 1.23 V versus RHE, which is among the highest reported for BiVO4-based photoelectrodes. Surface photovoltage and transient photocurrent measurements suggest a charge-transfer model in which photocurrents are enhanced by improved surface passivation, although the barrier at the Co–Pi/electrolyte interface limits the charge transfer.
关键词： charge transport,bismuth vanadate,Co–Pi passivation,water oxidation,metallic V13O16
更新于2025-09-23 15:23:52