Fe-doped TiO2 was prepared by the sol gel method and characterized by X-ray diffraction. All the Fe-doped TiO2 were composed of an anatase crystal form. The activity of the Fe-doped TiO2 for the degradation of the ges...Fe-doped TiO2 was prepared by the sol gel method and characterized by X-ray diffraction. All the Fe-doped TiO2 were composed of an anatase crystal form. The activity of the Fe-doped TiO2 for the degradation of the gesaprim commercial herbicide (which contains atrazine as active compound and formulating agents) was studied by varying the iron content during UV (15 W), visible light and solar irradiations. The visible light came from commercial saving energy lamps (13, 15 and 20 Watts). The gesaprim degradation rate depended on the iron content in the photo catalyst. The Fe-doped TiO2 (0.5% by weight of TiO2) showed higher TOC removal under visible light and was more active than the undoped TiO2 photo catalyst under the light irradiation sources tested. Over 90% of chemical oxygen demand abatement was achieved with both UV and visible light but less time was required to decrease the chemical oxygen demand content by using the catalyst doped with iron at 0.5% under visible light. It was observed that the degradation of gesaprim increased by increasing the iron content in the catalyst under visible light.展开更多
Fe-doped CuCrO_(2) catalyst CuCr_(1-x)Fe_xO_(2) series were prepared by the sol-gel method with different Fe contents.The structure and properties of the catalysts were investigated by XRD(X-ray diffraction),SEM(scann...Fe-doped CuCrO_(2) catalyst CuCr_(1-x)Fe_xO_(2) series were prepared by the sol-gel method with different Fe contents.The structure and properties of the catalysts were investigated by XRD(X-ray diffraction),SEM(scanning electron microscope),and XPS(X-ray photoelectron spectroscopy)and the purification effect on NO_(x) and PM was measured through simulated emission experiments.The results indicate that CuCrO_(2) catalyst has good catalytic activity,the maximum NO_(x) conversion rate can be up to 28.15%,and the ignition temperature of PM can be reduced to 285℃.When the molecular ratio of Cr:Fe=9:1,the catalyst can achieve better catalytic effect,the maximum NO_(x) conversion rate will be up to 30.25%and the PM ignition temperature can be reduced to 280℃.In addition,the catalytic activity of catalyst supported on different carriers was also studied.The results show that catalyst on SiC foam ceramic carrier has better catalytic activity than that on cordierite honeycomb ceramic carrier.The maximum NO_(x) conversion of CuCrO_(2) and CuCr_(0.9)Fe_(0.1)O_(2) can be increased by 0.72%and 1.33%respectively,and the PM ignition temperature can be further reduced by 15 and 5℃respectively.展开更多
This work aimed to study the efficiency of the reverse micelle(RM)preparation route in the syntheses of sub-5 nm Fe-doped CeO_(2)nanocrystals for boosting the visible-light-driven photocatalytic hydrogen production fr...This work aimed to study the efficiency of the reverse micelle(RM)preparation route in the syntheses of sub-5 nm Fe-doped CeO_(2)nanocrystals for boosting the visible-light-driven photocatalytic hydrogen production from methanol aqueous solutions.The effectiveness of confining precipitation reactions within micellar cages was evaluated through extensive physicochemical cha racterization.In particula r,the nominal composition(0-5 mol%Fe)was preserved as ascertained by ICP-MS analysis,and the absence of separate iron-containing crystalline phases was supported by X-ray diffraction.The effective aliovalent doping and modulation of the optical properties were investigated using UV-Vis,Raman,and photoluminescence spectroscopies.2.5 mol%iron was found to be an optimal content to achieve a significant decrease in the band gap,enhance the concentration of oxygen vacancy defects,and increase the charge carrier lifetime.The photocatalytic activity of Fe-doped CeO_(2)prepared at different Fe contents with RM preparation was studied and compared with undoped CeO_(2).The optimal iron load was identified to be2.5 mol%,achieving the highest hydrogen production(7566μmol L-1after 240 min under visible light).Moreover,for comparison,the conventional precipitation(P)method was adopted to prepare iron containing CeO_(2)at the optimal content(2.5 mol%Fe).The Fe-doped CeO_(2)catalyst prepared by RM showed a significantly higher hydrogen production than that obtained with the sample prepared by the P method.The optimal Fe-doped CeO_(2),prepared by the RM method,was stable for six reuse cycles.Moreover,the role of water in the mechanism of photocatalytic hydrogen evolution under visible light was studied through the test in the presence of D2O.The obtained results evidenced that hydrogen was produced from the reduction of H^(+)by the electrons promoted in the conduction band,while methanol was preferentially oxidized by the photogenerated positive holes.展开更多
It has been challenging for Fe(Ⅲ)regeneration in Fe-based photocatalysts for continuous peroxydisulfate(PDS)activation due to the lower ability to reduce Fe(Ⅲ).In this work,Fe-doped ultrathin VO_(2)(Fe-VO_(2))nanobe...It has been challenging for Fe(Ⅲ)regeneration in Fe-based photocatalysts for continuous peroxydisulfate(PDS)activation due to the lower ability to reduce Fe(Ⅲ).In this work,Fe-doped ultrathin VO_(2)(Fe-VO_(2))nanobelts were synthesized for purifying metronidazole(MNZ)via PDS activation.As an efficient Fentonlike catalyst for PDS activation,2 wt%Fe-doped VO_(2)can remove 98%of MNZ within 40 min and exhibits impressive recyclability.The synergistic effect of Fe-VO_(2)and Fe(Ⅲ)activated PDS boosted the photocatalytic performance.Moreover,SO_(4)•^(−),h+,O_(2)•^(−),^(1)O_(2),and•OH were the main reactive radicals.The effects of initial MNZ concentration,Fe-VO_(2),PDS dosage,and various anions/cations on MNZ removal by the Fe-VO_(2)/PDS/Vis system were studied.The intermediates of MNZ degradation and possible pathways were determined by density function theory(DFT)calculations and HPLC-MS.This study provided a sustainable technology using Fe-doped ultrathin VO_(2)nanobelts for photocatalytic PDS activation and decontamination of pharmaceutical wastewater.展开更多
The steel industry produces many byproducts, requiring extensive land for storage and causing significant environmental contamination. Industrial effluents discharged into water bodies negatively impact both aquatic e...The steel industry produces many byproducts, requiring extensive land for storage and causing significant environmental contamination. Industrial effluents discharged into water bodies negatively impact both aquatic ecosystems and human health. To solve this problem, this study synthesized a composite of titanium dioxide (TiO2) and steel slag nanocomposites (SSNC) at a 1:2 mass ratio to create a robust photocatalyst for the treatment of synthetic wastewater. The efficacy of this catalyst in degrading various dye pollutants, including methylene blue (MB), was tested under simulated solar light conditions. Comprehensive analyses were conducted to assess the physical and chemical characteristics, crystalline structure, energy gap, and point of zero charge of the composite. The TiO2-SSNC composite catalyst exhibited excellent stability, with a point of zero charge at 8.342 and an energy gap of 2.4 eV. The degradation process conformed to pseudo-first-order kinetics. Optimization of operational parameters was achieved through the response surface methodology. Reusability tests demonstrated that the TiO2-SSNC composite catalyst effectively degraded up to 93.41% of MB in the suspended mode and 92.03% in the coated mode after five cycles. Additionally, the degradation efficiencies for various dyes were significant, highlighting the potential of the composite for broad applications in industrial wastewater treatment. This study also explored the degradation mechanisms and identified byproducts, establishing a pathway for contaminant breakdown. The cost-benefit analysis revealed a total cost of 0.842 8 USD per cubic meter for each treatment activity, indicating low operational and production costs. These findings underscore the promise of the TiO2-SSNC composite as a cost-effective and efficient alternative for wastewater purification.展开更多
Synergistic interplays involving multiple active centers originating from TiO2 nanotube layers(TNT)and ruthenium(Ru)species comprising of both single atoms(SAs)and nanoparticles(NPs)augment the alkaline hydrogen evolu...Synergistic interplays involving multiple active centers originating from TiO2 nanotube layers(TNT)and ruthenium(Ru)species comprising of both single atoms(SAs)and nanoparticles(NPs)augment the alkaline hydrogen evolution reaction(HER)by enhancing Volmer kinetics from rapid water dissociation and improving Tafel kinetics from efficient H*desorption.Atomic layer deposition of Ru with 50 process cycles results in a mixture of Ru SAs and 2.8-0.4 nm NPs present on TNT layers,and it emerges with the highest HER activity among all the electrodes synthesized.A detailed study of the Ti and Ru species using different high-resolution techniques confirmed the presence of Ti^(3+)states and the coexistence of Ru SAs and NPs.With insights from literature,the role of Ti^(3+),appropriate work functions of TNT layers and Ru,and the synergistic effect of Ru SAs and Ru NPs in improving the performance of alkaline HER were elaborated and justified.The aforementioned characteristics led to a remarkable performance by having 9mV onset potentials and 33 mV dec^(-1) of Tafel slopes and a higher turnover frequency of 1.72 H2 s^(-1) at 30 mV.Besides,a notable stability from 28 h staircase chronopotentiometric measurements for TNT@Ru surpasses TNT@Pt in comparison.展开更多
In this paper, Fe-doped TiO_2 photocatalyst supported on hollow glass microbeads(Fe-TiO_2 /beads)is prepared by dip-coating method, which uses hollow glass microbeads as the carriers and tetrabutylorthotitanate [Ti(O...In this paper, Fe-doped TiO_2 photocatalyst supported on hollow glass microbeads(Fe-TiO_2 /beads)is prepared by dip-coating method, which uses hollow glass microbeads as the carriers and tetrabutylorthotitanate [Ti(OC_4H_9)_4] as the raw material. The phase structure, ingredient, morphologies, particle size and shell thickness of the products are characterized by X-ray powder diffraction(XRD), energy-dispersive spectroscopy(EDS) and field emission scanning electron microscope(FESEM). The feasibility of photocatylic degradation of Rhodamine B(Rh B) under illumination of UV-vis light is studied. The results show that the core-shell structure catalyst is composed of Fe-doped anatase TiO_2 and hollow glass microbeads, and the catalytic activity of the TiO_2 is markedly enhanced by Fe ion doping. The optimum concentration of Fe ion is 0.1%(molecular fraction) in the precursor and the photocatalytic activity can be increased to 98% compared with that of the undoped one. The presence of ferrum elements neither influences the transformation of anatase to rutile, nor creates new crystal phases. The possible mechanism of photocatalytic oxidation is also discussed.展开更多
Fe-doped In2O3 dilute magnetic semiconducting nanowires are fabricated on A u-deposited Si substrates by the chemical vapor deposition technique. It is confirmed by energy dispersive x-ray spectroscopy (EDS), x-ray ...Fe-doped In2O3 dilute magnetic semiconducting nanowires are fabricated on A u-deposited Si substrates by the chemical vapor deposition technique. It is confirmed by energy dispersive x-ray spectroscopy (EDS), x-ray photoelectron spectroscopy (XPS) and Raman spectroscopy that Fe has been successfully doped into lattices of In2O3 nanowires. The EDS measurements reveal a large amount of oxygen vacancies existing in the Fe-doped In2O3 nanowires. The Fe dopant exists as a mixture of Fe2+ and Fe3+, as revealed by the XPS. The origin of room-temperature ferromagnetism in Fe-doped In2O3 nanowires is explained by the bound magnetic polaron model.展开更多
The structural evolution of Fe-doped TiO2 by high-energy ball milling was investigated by X-ray diffraction and Mǒssbauer spectroscopy, The results show that the original anatase-TiO2 transforms to srilankite-type an...The structural evolution of Fe-doped TiO2 by high-energy ball milling was investigated by X-ray diffraction and Mǒssbauer spectroscopy, The results show that the original anatase-TiO2 transforms to srilankite-type and rutile-type during ball milling. Iron atoms are preferable to dissolve in rutile-TiO2 and there are two relative doublets appearing in Mǒssbauer spectra. A doublet is found in the condition of Fe atoms dissolved in srilankite TiO2 lattice. Mǒssbauer spectra show that the composition distribution is nonuniform in TiO2 during the mechanical alloying with Fe atoms rich at the interface or surface of TiO2 crystalline.展开更多
文摘Fe-doped TiO2 was prepared by the sol gel method and characterized by X-ray diffraction. All the Fe-doped TiO2 were composed of an anatase crystal form. The activity of the Fe-doped TiO2 for the degradation of the gesaprim commercial herbicide (which contains atrazine as active compound and formulating agents) was studied by varying the iron content during UV (15 W), visible light and solar irradiations. The visible light came from commercial saving energy lamps (13, 15 and 20 Watts). The gesaprim degradation rate depended on the iron content in the photo catalyst. The Fe-doped TiO2 (0.5% by weight of TiO2) showed higher TOC removal under visible light and was more active than the undoped TiO2 photo catalyst under the light irradiation sources tested. Over 90% of chemical oxygen demand abatement was achieved with both UV and visible light but less time was required to decrease the chemical oxygen demand content by using the catalyst doped with iron at 0.5% under visible light. It was observed that the degradation of gesaprim increased by increasing the iron content in the catalyst under visible light.
基金Funded by National Natural Science Foundation of China(No.52494933)。
文摘Fe-doped CuCrO_(2) catalyst CuCr_(1-x)Fe_xO_(2) series were prepared by the sol-gel method with different Fe contents.The structure and properties of the catalysts were investigated by XRD(X-ray diffraction),SEM(scanning electron microscope),and XPS(X-ray photoelectron spectroscopy)and the purification effect on NO_(x) and PM was measured through simulated emission experiments.The results indicate that CuCrO_(2) catalyst has good catalytic activity,the maximum NO_(x) conversion rate can be up to 28.15%,and the ignition temperature of PM can be reduced to 285℃.When the molecular ratio of Cr:Fe=9:1,the catalyst can achieve better catalytic effect,the maximum NO_(x) conversion rate will be up to 30.25%and the PM ignition temperature can be reduced to 280℃.In addition,the catalytic activity of catalyst supported on different carriers was also studied.The results show that catalyst on SiC foam ceramic carrier has better catalytic activity than that on cordierite honeycomb ceramic carrier.The maximum NO_(x) conversion of CuCrO_(2) and CuCr_(0.9)Fe_(0.1)O_(2) can be increased by 0.72%and 1.33%respectively,and the PM ignition temperature can be further reduced by 15 and 5℃respectively.
基金funding from the"Ministero dell'Universitàe della Ricerca(MUR)"(Italy)under the"Dipartimento di Eccellenza 2018-2022"program.
文摘This work aimed to study the efficiency of the reverse micelle(RM)preparation route in the syntheses of sub-5 nm Fe-doped CeO_(2)nanocrystals for boosting the visible-light-driven photocatalytic hydrogen production from methanol aqueous solutions.The effectiveness of confining precipitation reactions within micellar cages was evaluated through extensive physicochemical cha racterization.In particula r,the nominal composition(0-5 mol%Fe)was preserved as ascertained by ICP-MS analysis,and the absence of separate iron-containing crystalline phases was supported by X-ray diffraction.The effective aliovalent doping and modulation of the optical properties were investigated using UV-Vis,Raman,and photoluminescence spectroscopies.2.5 mol%iron was found to be an optimal content to achieve a significant decrease in the band gap,enhance the concentration of oxygen vacancy defects,and increase the charge carrier lifetime.The photocatalytic activity of Fe-doped CeO_(2)prepared at different Fe contents with RM preparation was studied and compared with undoped CeO_(2).The optimal iron load was identified to be2.5 mol%,achieving the highest hydrogen production(7566μmol L-1after 240 min under visible light).Moreover,for comparison,the conventional precipitation(P)method was adopted to prepare iron containing CeO_(2)at the optimal content(2.5 mol%Fe).The Fe-doped CeO_(2)catalyst prepared by RM showed a significantly higher hydrogen production than that obtained with the sample prepared by the P method.The optimal Fe-doped CeO_(2),prepared by the RM method,was stable for six reuse cycles.Moreover,the role of water in the mechanism of photocatalytic hydrogen evolution under visible light was studied through the test in the presence of D2O.The obtained results evidenced that hydrogen was produced from the reduction of H^(+)by the electrons promoted in the conduction band,while methanol was preferentially oxidized by the photogenerated positive holes.
基金the financial supports from the National Key Research and Development Program of China(Nos.2021YFB3500600,2021YFB3500605,2022YFB3504100)Key R&D Program of Jiangsu Province(No.BE2022142)+6 种基金Ministry of Education Chunhui plan international cooperation project(No.202200554)National Natural Science Foundation of China(No.grant 22208170)Natural Science Foundation of Inner Mongolia(No.2021BS02016)Jiangsu International Cooperation Project(No.BZ2021018)Nanjing Science and Technology Top Experts Gathering Plan,and Open Foundation of State Environmental Protection Key Laboratory of Soil Environmental Management and Pollution Control(No.SEMPC2023004)Cooperation Foundation for the Chunhui Plan Program of Ministry of Education of China(No.202200554)Open Project Program of Key Laboratory of Opticelectric Sensing and Analytical Chemistry for Life Science(No.M2024-7),MOE。
文摘It has been challenging for Fe(Ⅲ)regeneration in Fe-based photocatalysts for continuous peroxydisulfate(PDS)activation due to the lower ability to reduce Fe(Ⅲ).In this work,Fe-doped ultrathin VO_(2)(Fe-VO_(2))nanobelts were synthesized for purifying metronidazole(MNZ)via PDS activation.As an efficient Fentonlike catalyst for PDS activation,2 wt%Fe-doped VO_(2)can remove 98%of MNZ within 40 min and exhibits impressive recyclability.The synergistic effect of Fe-VO_(2)and Fe(Ⅲ)activated PDS boosted the photocatalytic performance.Moreover,SO_(4)•^(−),h+,O_(2)•^(−),^(1)O_(2),and•OH were the main reactive radicals.The effects of initial MNZ concentration,Fe-VO_(2),PDS dosage,and various anions/cations on MNZ removal by the Fe-VO_(2)/PDS/Vis system were studied.The intermediates of MNZ degradation and possible pathways were determined by density function theory(DFT)calculations and HPLC-MS.This study provided a sustainable technology using Fe-doped ultrathin VO_(2)nanobelts for photocatalytic PDS activation and decontamination of pharmaceutical wastewater.
基金supported by the Department of Chemical and Petrochemical Engineering,Egypt-Japan University of Science and Technology.
文摘The steel industry produces many byproducts, requiring extensive land for storage and causing significant environmental contamination. Industrial effluents discharged into water bodies negatively impact both aquatic ecosystems and human health. To solve this problem, this study synthesized a composite of titanium dioxide (TiO2) and steel slag nanocomposites (SSNC) at a 1:2 mass ratio to create a robust photocatalyst for the treatment of synthetic wastewater. The efficacy of this catalyst in degrading various dye pollutants, including methylene blue (MB), was tested under simulated solar light conditions. Comprehensive analyses were conducted to assess the physical and chemical characteristics, crystalline structure, energy gap, and point of zero charge of the composite. The TiO2-SSNC composite catalyst exhibited excellent stability, with a point of zero charge at 8.342 and an energy gap of 2.4 eV. The degradation process conformed to pseudo-first-order kinetics. Optimization of operational parameters was achieved through the response surface methodology. Reusability tests demonstrated that the TiO2-SSNC composite catalyst effectively degraded up to 93.41% of MB in the suspended mode and 92.03% in the coated mode after five cycles. Additionally, the degradation efficiencies for various dyes were significant, highlighting the potential of the composite for broad applications in industrial wastewater treatment. This study also explored the degradation mechanisms and identified byproducts, establishing a pathway for contaminant breakdown. The cost-benefit analysis revealed a total cost of 0.842 8 USD per cubic meter for each treatment activity, indicating low operational and production costs. These findings underscore the promise of the TiO2-SSNC composite as a cost-effective and efficient alternative for wastewater purification.
基金support from the European Union Horizon 2020 program(project HERMES,nr.952184)the Ministry of Education,Youth and Sports of the Czech Republic for supporting CEMNAT(LM2023037)+1 种基金Czech-NanoLab(LM2023051)infrastructures for providing ALD,SEM,EDX,XPS,TEM,and XRDCzech Science Foundation(project 23-08019X,EXPRO).
文摘Synergistic interplays involving multiple active centers originating from TiO2 nanotube layers(TNT)and ruthenium(Ru)species comprising of both single atoms(SAs)and nanoparticles(NPs)augment the alkaline hydrogen evolution reaction(HER)by enhancing Volmer kinetics from rapid water dissociation and improving Tafel kinetics from efficient H*desorption.Atomic layer deposition of Ru with 50 process cycles results in a mixture of Ru SAs and 2.8-0.4 nm NPs present on TNT layers,and it emerges with the highest HER activity among all the electrodes synthesized.A detailed study of the Ti and Ru species using different high-resolution techniques confirmed the presence of Ti^(3+)states and the coexistence of Ru SAs and NPs.With insights from literature,the role of Ti^(3+),appropriate work functions of TNT layers and Ru,and the synergistic effect of Ru SAs and Ru NPs in improving the performance of alkaline HER were elaborated and justified.The aforementioned characteristics led to a remarkable performance by having 9mV onset potentials and 33 mV dec^(-1) of Tafel slopes and a higher turnover frequency of 1.72 H2 s^(-1) at 30 mV.Besides,a notable stability from 28 h staircase chronopotentiometric measurements for TNT@Ru surpasses TNT@Pt in comparison.
文摘In this paper, Fe-doped TiO_2 photocatalyst supported on hollow glass microbeads(Fe-TiO_2 /beads)is prepared by dip-coating method, which uses hollow glass microbeads as the carriers and tetrabutylorthotitanate [Ti(OC_4H_9)_4] as the raw material. The phase structure, ingredient, morphologies, particle size and shell thickness of the products are characterized by X-ray powder diffraction(XRD), energy-dispersive spectroscopy(EDS) and field emission scanning electron microscope(FESEM). The feasibility of photocatylic degradation of Rhodamine B(Rh B) under illumination of UV-vis light is studied. The results show that the core-shell structure catalyst is composed of Fe-doped anatase TiO_2 and hollow glass microbeads, and the catalytic activity of the TiO_2 is markedly enhanced by Fe ion doping. The optimum concentration of Fe ion is 0.1%(molecular fraction) in the precursor and the photocatalytic activity can be increased to 98% compared with that of the undoped one. The presence of ferrum elements neither influences the transformation of anatase to rutile, nor creates new crystal phases. The possible mechanism of photocatalytic oxidation is also discussed.
基金Supported by the National Basic Research Program of China under Grant Nos 2014CB921101,2014CB921103 and2013CB922103the National Natural Science Foundation of China under Grant Nos 11274003,61176088 and 61274102+1 种基金the Program for the New Century Excellent Talents in University under Grant No NCET-11-0240the PAPD Project,and the Fundamental Research Funds for the Central Universities
文摘Fe-doped In2O3 dilute magnetic semiconducting nanowires are fabricated on A u-deposited Si substrates by the chemical vapor deposition technique. It is confirmed by energy dispersive x-ray spectroscopy (EDS), x-ray photoelectron spectroscopy (XPS) and Raman spectroscopy that Fe has been successfully doped into lattices of In2O3 nanowires. The EDS measurements reveal a large amount of oxygen vacancies existing in the Fe-doped In2O3 nanowires. The Fe dopant exists as a mixture of Fe2+ and Fe3+, as revealed by the XPS. The origin of room-temperature ferromagnetism in Fe-doped In2O3 nanowires is explained by the bound magnetic polaron model.
文摘The structural evolution of Fe-doped TiO2 by high-energy ball milling was investigated by X-ray diffraction and Mǒssbauer spectroscopy, The results show that the original anatase-TiO2 transforms to srilankite-type and rutile-type during ball milling. Iron atoms are preferable to dissolve in rutile-TiO2 and there are two relative doublets appearing in Mǒssbauer spectra. A doublet is found in the condition of Fe atoms dissolved in srilankite TiO2 lattice. Mǒssbauer spectra show that the composition distribution is nonuniform in TiO2 during the mechanical alloying with Fe atoms rich at the interface or surface of TiO2 crystalline.