Surface of TiO2 nanoparticles was modified with the in situ chemical oxidative polymerization of aniline. Polyaniline modified TiO2 nanoparticles （PANI-TiO2） were characterized with the FT-IR, XRD, SEM and TEM techn...Surface of TiO2 nanoparticles was modified with the in situ chemical oxidative polymerization of aniline. Polyaniline modified TiO2 nanoparticles （PANI-TiO2） were characterized with the FT-IR, XRD, SEM and TEM techniques. Results confirmed that PANI was grafted successfully on the surface of TiO2 nanoparticles, therefore agglomeration of nanoparticles decreased dramatically. Polyvinyl chloride nanocomposites filled with 1 wt%-5 wt% of PANI-TiO2 and TiO2 nanoparticles were prepared via the solution blending method. PVC nanocomposites were analyzed with FT-IR, XRD, SEM, TG/DTA, DSC and tensile test techniques. Effect of PANI as surface modifier of nanoparticles was discussed according to the final properties of PVC nanocomposites. Results demonstrated that deposition of PANI on the surface of TiO2 nanoparticles improved the interfacial adhesion between the constituents of nanocomposites, which resulted in better dispersion of nanoparticles in the PVC matrix. Also PVC/PANI-TiO2 nanocomposites showed higher thennal resistance, tensile strength and Young＇s modulus compared to those of unfilled PVC and PVC/TiO2 nanocomposites.展开更多
Due to its importance in hydrogen production during the photolysis process of aqueous suspensions process, mixed TiO2/V2O5 metal-oxide semiconductors were prepared and subjected to crystal structure investigation usin...Due to its importance in hydrogen production during the photolysis process of aqueous suspensions process, mixed TiO2/V2O5 metal-oxide semiconductors were prepared and subjected to crystal structure investigation using X-ray technique. The photoelectrochemical behavior of these TiO2/V2O5 was investigated by photolysis of aqueous suspensions of these oxides containing [Fe(CN)6]4-. X-ray diffraction analysis indicated that the TiO2 crystallites grow in the (1 0 1) direction, while The V2O5 crystallites seem to be growing in the (4 2 0) direction, with increasing concentration of V2O5. Photolysis studies show that photochemical activities that maintained the [Fe(CN)6]4/[Fe(CN)6]3- redox reversibility increased by increasing V2O5 up to 50% and then decreased at greater percentages. Aqueous nano systems used in these studies retained their stability as indicated by the reproducibility of their photo-catalytic activities.展开更多
Rutile phase exhibits higher refractive index and h id ing power, good chemical stability, and is becoming a candidate material for the high-temperature separation and catalysis applications. The thermodynamically sta...Rutile phase exhibits higher refractive index and h id ing power, good chemical stability, and is becoming a candidate material for the high-temperature separation and catalysis applications. The thermodynamically stable feature of rutile among the three polymorphs of TiO 2 usually hinders ob taining nano-sized rutile phase by a conventional calcining way. However, acid peptization of amorphous TiO 2 is favorable to the formation of rutile phase. I n this work, well-crystallized and well-dispersed rod-like rutile particles w ith specific surface areas of 49.1 and 35.0 m 2/g were prepared by hydrothermal ly treating the acid peptized TiO 2 amorphous sols at relatively low temperatur es of 200 ℃ or 240 ℃, respectively. The formation of non-touching rutile part icles is attributed to high long-range electrostatic forces between particles i n the presence of the high concentration of the peptizer. The acid peptization w ould easily break the ≡Ti-O-Ti≡ bonds to form ≡Ti-OH or HO-Ti-OH species depending on the amount of acid, and create conditions for the formation of rut ile nuclei after structural rearrangements.展开更多
γ-Fe nano-particles with size of 20-40 nm were produced by SF6-sensitized CW CO2 laser-induced gaseous pyrolysis of Fe(Co) 5, The γ-Fe stabte in reaction zone at above 910℃ was formed.The rapid quenching prevents f...γ-Fe nano-particles with size of 20-40 nm were produced by SF6-sensitized CW CO2 laser-induced gaseous pyrolysis of Fe(Co) 5, The γ-Fe stabte in reaction zone at above 910℃ was formed.The rapid quenching prevents from the γ-Fe transforming to α-Fe as rapidly cooling from high temperature to room temperature, The characteristics of the particles were examined at room temperature by TEM. electron diffraction and XRD. It was proved that about 70% of γ-Fe phase in the particles was present. In addition. the lattice constant of the γ-Fe was 0.364 nm in place of 0.360 nm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
We prepared TiO 2(anatase) and Sn doped TiO 2 nanoparticlate film by Plasma enhanced Chemical Vapor Deposition(PECVD) method. XRD and XPS experiments showed that Sn was doped into the lattice of TiO 2 with a ratio of ...We prepared TiO 2(anatase) and Sn doped TiO 2 nanoparticlate film by Plasma enhanced Chemical Vapor Deposition(PECVD) method. XRD and XPS experiments showed that Sn was doped into the lattice of TiO 2 with a ratio of n (Sn)∶ n (Ti)=1∶10 . Sn doping largely enhanced the photocatalytic activity of TiO 2 film for phenol degradation. The enhancement in photoactivity by doping was discussed, based on the characterization with AFM, FTIR and EFISPS. Sn doping produced localized level of Sn 4+ in the band gap of TiO 2, about 0.4 eV below the conduction band, which could capture photogenerated electrons and reduce O 2 adsorbed on the surface of TiO 2 film, thus accelerated the photocatalytic reaction.展开更多
The transition metal ion doped TiO 2 nanoparticles were prepared with hydrothermal method, and the effects of doping different metal ions on the ability of TiO 2 in photocatalyzing degradation of rhodamine B(RB) were ...The transition metal ion doped TiO 2 nanoparticles were prepared with hydrothermal method, and the effects of doping different metal ions on the ability of TiO 2 in photocatalyzing degradation of rhodamine B(RB) were studied. The results showed that the doping of Fe 3+ , Co 2+ , Ni 2+ and Cr 3+ in TiO 2 nanoparticles made the photocatalytic efficiency of the TiO 2 particles reduce and the higher the initial content of Fe 3+ , the lower the ability of TiO 2 in photocatalyzing the degradation of RB. But the doping of Zn 2+ and Cd 2+ , especially Zn 2+ , made the photocatalytic efficiency of the TiO 2 particles enhance, showing a great increase of the rate constant( k ) and the initial reaction rate( r ini ).展开更多
基金financially supported by the University of Tabriz
文摘Surface of TiO2 nanoparticles was modified with the in situ chemical oxidative polymerization of aniline. Polyaniline modified TiO2 nanoparticles （PANI-TiO2） were characterized with the FT-IR, XRD, SEM and TEM techniques. Results confirmed that PANI was grafted successfully on the surface of TiO2 nanoparticles, therefore agglomeration of nanoparticles decreased dramatically. Polyvinyl chloride nanocomposites filled with 1 wt%-5 wt% of PANI-TiO2 and TiO2 nanoparticles were prepared via the solution blending method. PVC nanocomposites were analyzed with FT-IR, XRD, SEM, TG/DTA, DSC and tensile test techniques. Effect of PANI as surface modifier of nanoparticles was discussed according to the final properties of PVC nanocomposites. Results demonstrated that deposition of PANI on the surface of TiO2 nanoparticles improved the interfacial adhesion between the constituents of nanocomposites, which resulted in better dispersion of nanoparticles in the PVC matrix. Also PVC/PANI-TiO2 nanocomposites showed higher thennal resistance, tensile strength and Young＇s modulus compared to those of unfilled PVC and PVC/TiO2 nanocomposites.
文摘Due to its importance in hydrogen production during the photolysis process of aqueous suspensions process, mixed TiO2/V2O5 metal-oxide semiconductors were prepared and subjected to crystal structure investigation using X-ray technique. The photoelectrochemical behavior of these TiO2/V2O5 was investigated by photolysis of aqueous suspensions of these oxides containing [Fe(CN)6]4-. X-ray diffraction analysis indicated that the TiO2 crystallites grow in the (1 0 1) direction, while The V2O5 crystallites seem to be growing in the (4 2 0) direction, with increasing concentration of V2O5. Photolysis studies show that photochemical activities that maintained the [Fe(CN)6]4/[Fe(CN)6]3- redox reversibility increased by increasing V2O5 up to 50% and then decreased at greater percentages. Aqueous nano systems used in these studies retained their stability as indicated by the reproducibility of their photo-catalytic activities.
文摘Rutile phase exhibits higher refractive index and h id ing power, good chemical stability, and is becoming a candidate material for the high-temperature separation and catalysis applications. The thermodynamically stable feature of rutile among the three polymorphs of TiO 2 usually hinders ob taining nano-sized rutile phase by a conventional calcining way. However, acid peptization of amorphous TiO 2 is favorable to the formation of rutile phase. I n this work, well-crystallized and well-dispersed rod-like rutile particles w ith specific surface areas of 49.1 and 35.0 m 2/g were prepared by hydrothermal ly treating the acid peptized TiO 2 amorphous sols at relatively low temperatur es of 200 ℃ or 240 ℃, respectively. The formation of non-touching rutile part icles is attributed to high long-range electrostatic forces between particles i n the presence of the high concentration of the peptizer. The acid peptization w ould easily break the ≡Ti-O-Ti≡ bonds to form ≡Ti-OH or HO-Ti-OH species depending on the amount of acid, and create conditions for the formation of rut ile nuclei after structural rearrangements.
文摘γ-Fe nano-particles with size of 20-40 nm were produced by SF6-sensitized CW CO2 laser-induced gaseous pyrolysis of Fe(Co) 5, The γ-Fe stabte in reaction zone at above 910℃ was formed.The rapid quenching prevents from the γ-Fe transforming to α-Fe as rapidly cooling from high temperature to room temperature, The characteristics of the particles were examined at room temperature by TEM. electron diffraction and XRD. It was proved that about 70% of γ-Fe phase in the particles was present. In addition. the lattice constant of the γ-Fe was 0.364 nm in place of 0.360 nm
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We prepared TiO 2(anatase) and Sn doped TiO 2 nanoparticlate film by Plasma enhanced Chemical Vapor Deposition(PECVD) method. XRD and XPS experiments showed that Sn was doped into the lattice of TiO 2 with a ratio of n (Sn)∶ n (Ti)=1∶10 . Sn doping largely enhanced the photocatalytic activity of TiO 2 film for phenol degradation. The enhancement in photoactivity by doping was discussed, based on the characterization with AFM, FTIR and EFISPS. Sn doping produced localized level of Sn 4+ in the band gap of TiO 2, about 0.4 eV below the conduction band, which could capture photogenerated electrons and reduce O 2 adsorbed on the surface of TiO 2 film, thus accelerated the photocatalytic reaction.
文摘The transition metal ion doped TiO 2 nanoparticles were prepared with hydrothermal method, and the effects of doping different metal ions on the ability of TiO 2 in photocatalyzing degradation of rhodamine B(RB) were studied. The results showed that the doping of Fe 3+ , Co 2+ , Ni 2+ and Cr 3+ in TiO 2 nanoparticles made the photocatalytic efficiency of the TiO 2 particles reduce and the higher the initial content of Fe 3+ , the lower the ability of TiO 2 in photocatalyzing the degradation of RB. But the doping of Zn 2+ and Cd 2+ , especially Zn 2+ , made the photocatalytic efficiency of the TiO 2 particles enhance, showing a great increase of the rate constant( k ) and the initial reaction rate( r ini ).
