Antoine Farcy , Stéphanie D. Lambert , Maxine Mathy , Louise Lejeune , Pierre Eloy , Sophie Hermans , Julien G. Mahy
{"title":"uv -可见光下Ta、V、nb掺杂TiO2光催化和电催化降解对硝基苯酚的优化研究","authors":"Antoine Farcy , Stéphanie D. Lambert , Maxine Mathy , Louise Lejeune , Pierre Eloy , Sophie Hermans , Julien G. Mahy","doi":"10.1016/j.jphotochem.2025.116453","DOIUrl":null,"url":null,"abstract":"<div><div>The objective of this study is to investigate the enhancement of TiO<sub>2</sub> photocatalytic activity under UV/visible and visible light by doping with tantalum (Ta), vanadium (V) or niobium (Nb) precursors. Thus, TiO<sub>2</sub>-based photocatalysts are prepared at room temperature via aqueous sol–gel synthesis. These photocatalysts are doped with different molar ratios of dopants. The physicochemical properties of the obtained photocatalysts are characterized using various complementary techniques. X-ray diffraction (XRD) is used to determine the distribution of different crystalline phases of TiO<sub>2</sub> and the proportion of amorphous TiO<sub>2</sub> in the samples. BET measurements give textural properties with specific surface area reaching up to 292 m<sup>2</sup>/g and TEM images illustrating their spherical morphology. Inductively coupled plasma atomic emission spectroscopy (ICP-AES), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) analyses confirmed the presence of Ti, O and Ta, V or Nb elements in the samples. Additionally, XPS spectra highlights the incorporation of nitrogen in the undoped synthesized TiO<sub>2</sub>. Additionally, band gap widths measured by UV–vis diffuse reflectance spectroscopy (DRUS) are done to see the impact of the dopants on the bandgap, with V-doping reducing its value from 2.95 to 1.88 eV. A screening of the photocatalytic activity of undoped and doped photocatalysts is carried out by evaluating the degradation of p-nitrophenol under UV–visible light (300 < λ < 800 nm) and visible light only (395 < λ < 800 nm). This study suggests that photocatalytic activity is significantly influenced by the nature and dopant content. Photocatalytic tests show an improvement in the activity of the photocatalyst when doped with tantalum and niobium (from 22 % with undoped TiO<sub>2</sub> under visible light to 37 % and 55 % with the best Ta and Nb-doped samples respectively), while a notable decrease in activity is observed with vanadium doping (dropping to 3–12 % with the V-doped series). Finally, a preliminary electrophotocatalysis experimental setup is implemented and appears to show an improvement in the mineralization of the PNP solution when the anode is coated with layers of the best doped-TiO<sub>2</sub> material (Nd doping), compared to an uncoated anode (the mineralization rate increases from 72 % to 94 %).</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"467 ","pages":"Article 116453"},"PeriodicalIF":4.1000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimization of Ta-, V-, or Nb-doped TiO2 for photocatalytic and electrophotocatalytic degradation of p-nitrophenol under UV–visible light\",\"authors\":\"Antoine Farcy , Stéphanie D. Lambert , Maxine Mathy , Louise Lejeune , Pierre Eloy , Sophie Hermans , Julien G. Mahy\",\"doi\":\"10.1016/j.jphotochem.2025.116453\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The objective of this study is to investigate the enhancement of TiO<sub>2</sub> photocatalytic activity under UV/visible and visible light by doping with tantalum (Ta), vanadium (V) or niobium (Nb) precursors. Thus, TiO<sub>2</sub>-based photocatalysts are prepared at room temperature via aqueous sol–gel synthesis. These photocatalysts are doped with different molar ratios of dopants. The physicochemical properties of the obtained photocatalysts are characterized using various complementary techniques. X-ray diffraction (XRD) is used to determine the distribution of different crystalline phases of TiO<sub>2</sub> and the proportion of amorphous TiO<sub>2</sub> in the samples. BET measurements give textural properties with specific surface area reaching up to 292 m<sup>2</sup>/g and TEM images illustrating their spherical morphology. Inductively coupled plasma atomic emission spectroscopy (ICP-AES), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) analyses confirmed the presence of Ti, O and Ta, V or Nb elements in the samples. Additionally, XPS spectra highlights the incorporation of nitrogen in the undoped synthesized TiO<sub>2</sub>. Additionally, band gap widths measured by UV–vis diffuse reflectance spectroscopy (DRUS) are done to see the impact of the dopants on the bandgap, with V-doping reducing its value from 2.95 to 1.88 eV. A screening of the photocatalytic activity of undoped and doped photocatalysts is carried out by evaluating the degradation of p-nitrophenol under UV–visible light (300 < λ < 800 nm) and visible light only (395 < λ < 800 nm). This study suggests that photocatalytic activity is significantly influenced by the nature and dopant content. Photocatalytic tests show an improvement in the activity of the photocatalyst when doped with tantalum and niobium (from 22 % with undoped TiO<sub>2</sub> under visible light to 37 % and 55 % with the best Ta and Nb-doped samples respectively), while a notable decrease in activity is observed with vanadium doping (dropping to 3–12 % with the V-doped series). Finally, a preliminary electrophotocatalysis experimental setup is implemented and appears to show an improvement in the mineralization of the PNP solution when the anode is coated with layers of the best doped-TiO<sub>2</sub> material (Nd doping), compared to an uncoated anode (the mineralization rate increases from 72 % to 94 %).</div></div>\",\"PeriodicalId\":16782,\"journal\":{\"name\":\"Journal of Photochemistry and Photobiology A-chemistry\",\"volume\":\"467 \",\"pages\":\"Article 116453\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Photochemistry and Photobiology A-chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1010603025001935\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology A-chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1010603025001935","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Optimization of Ta-, V-, or Nb-doped TiO2 for photocatalytic and electrophotocatalytic degradation of p-nitrophenol under UV–visible light
The objective of this study is to investigate the enhancement of TiO2 photocatalytic activity under UV/visible and visible light by doping with tantalum (Ta), vanadium (V) or niobium (Nb) precursors. Thus, TiO2-based photocatalysts are prepared at room temperature via aqueous sol–gel synthesis. These photocatalysts are doped with different molar ratios of dopants. The physicochemical properties of the obtained photocatalysts are characterized using various complementary techniques. X-ray diffraction (XRD) is used to determine the distribution of different crystalline phases of TiO2 and the proportion of amorphous TiO2 in the samples. BET measurements give textural properties with specific surface area reaching up to 292 m2/g and TEM images illustrating their spherical morphology. Inductively coupled plasma atomic emission spectroscopy (ICP-AES), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) analyses confirmed the presence of Ti, O and Ta, V or Nb elements in the samples. Additionally, XPS spectra highlights the incorporation of nitrogen in the undoped synthesized TiO2. Additionally, band gap widths measured by UV–vis diffuse reflectance spectroscopy (DRUS) are done to see the impact of the dopants on the bandgap, with V-doping reducing its value from 2.95 to 1.88 eV. A screening of the photocatalytic activity of undoped and doped photocatalysts is carried out by evaluating the degradation of p-nitrophenol under UV–visible light (300 < λ < 800 nm) and visible light only (395 < λ < 800 nm). This study suggests that photocatalytic activity is significantly influenced by the nature and dopant content. Photocatalytic tests show an improvement in the activity of the photocatalyst when doped with tantalum and niobium (from 22 % with undoped TiO2 under visible light to 37 % and 55 % with the best Ta and Nb-doped samples respectively), while a notable decrease in activity is observed with vanadium doping (dropping to 3–12 % with the V-doped series). Finally, a preliminary electrophotocatalysis experimental setup is implemented and appears to show an improvement in the mineralization of the PNP solution when the anode is coated with layers of the best doped-TiO2 material (Nd doping), compared to an uncoated anode (the mineralization rate increases from 72 % to 94 %).
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.