ABSTRACT
La-Co-O mixed oxides (LCO) were prepared by co-precipitation method with the presence of polyethylene glycol (PEG) as dispersant. The influence of adding different molecular weight of PEG (0, 2 000, 6 000, 20 000 g·mol-1) on the physicochemical and catalytic properties of La-Co-O mixed oxides for total oxidation of benzene was investigated. The samples were characterized by means of N2 physical adsorption, X-ray diffraction (XRD), scanning electron microscopy (SEM), temperature-programmed reduction by H2 (H2-TPR), temperature-programmed desorption of O2 (O2-TPD), and X-ray photoelectron spectroscopy (XPS). The order of catalytic activity was found to be LCO-PEG6000>LCO>LCO-PG20000>LCO-PG2000. Particularly, LCO-PEG6000 exhibited benzene conversion of 99% at temperature as low as 383 â, which was 126 â lower than that of LCO. The characterization result reveals that all samples had a BET surface area of about 9ï½10 m2·g-1. The XRD result shows that on all samples LaCoO3 perovskite was mainly formed together with a small amount of La2O3 and Co3O4. The addition of PEG was favorable for the formation of LaCoO3 perovskite. Particularly, the addition of PEG-6000 effectively suppressed the agglomeration of LaCoO3 perovskite, giving rise to small and uniform particles as observed by SEM. Moreover, the results of H2-TPR and O2-TPD indicate that the obtained La-Co-O mixed oxides showed higher reducibility and lattice oxygen mobility, and the Co 2p XPS analysis suggests that more surface Co3+ active species were presented by the addition of PEG-6000. These properties are thought to contribute to the high activity in benzene total oxidation.
ABSTRACT
Ordered mesoporous γ-alumina (OMA), Ce-doped, Zr-doped and Ce-Zr-codoped OMA samples were synthesized in a sol-gel system with P123 as the soft template, both salicylic acid and citric acid as the assistant templates. The results show that the incorporations of either cerium or zirconium or both are able to improve the thermal stability of OMA. The capability to preserve the structural ordering and suppress the phase transition from γ-Al2O3 to α-Al2O3 at high temperature observed on the doped OMA is due to the formation of CeO2, ZrO2 or Ce(x)Zr(1-x)O2 phase, which is capable of protecting OMA from the structural collapse by sintering and phase transition.
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In this work, we study the enhancement of Raman signals and photocatalytic activity of Ag/ZnO heterojunctions with an Ag content of 1 at.%, which were synthesized by photochemical deposition of Ag nanoparticles onto pre-synthesized ZnO nanorods. A strong interaction between Ag and ZnO nanocrystals were evidenced by XPS and UV-vis spectroscopy. The binding energy of Ag nanoparticles shifts toward lower energy compared to that of pure Ag nanoparticles, revealing that electrons transfer from Ag to the ZnO nanocrystals. The red shift of the plasmon absorption peak of Ag nanoparticles in Ag/ZnO heterojunctions further confirms the strong interaction between the two components. This strong interaction, arising from the coupling between Ag and ZnO nanocrystals, is responsible for the enhancement of Raman signals and photocatalytic activity of the Ag/ZnO heterojunctions.
ABSTRACT
Highly dispersed ceria-zirconia supported on ordered mesoporous alumina, showing higher thermal stability up to 900 °C, has been successfully synthesized via a sol-gel process associated with P123 as the template in ethanol solvent.
ABSTRACT
Ternary oxide Zn(2)Ti(3)O(8) nanowires were first synthesized and used as the anode material in a rechargeable lithium-ion battery, which displayed a very reversible charge-discharge capacity and excellent cycling stability.
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A network-structured SnO(2)/ZnO heterojunction nanocatalyst with high photocatalytic activity was successfully synthesized through a simple two-step solvothermal method. The as-synthesized samples are characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy, N(2) physical adsorption, and UV-vis spectroscopy. The results show that the SnO(2)/ZnO sample with a molar ratio of Sn/Zn = 1 is a mesoporous composite material composed of SnO(2) and ZnO. The photocatalytic activity of SnO(2)/ZnO heterojunction nanocatalysts for the degradation of methyl orange is much higher than those of solvothermally synthesized SnO(2) and ZnO samples, which can be attributed to the SnO(2)-ZnO heterojunction, the pore structure, and higher Brunauer-Emmett-Teller (BET) surface area of the sample: (1) The SnO(2)-ZnO heterojunction improves the separation of photogenerated electron-hole pairs due to the potential energy differences between SnO(2) and ZnO, thus enhancing the photocatalytic activity. (2) The SnO(2)/ZnO sample might possess more surface reaction sites and adsorb and transport more dye molecules due to the higher BET surface area and many pore channels, also leading to higher photocatalytic activity.
Subject(s)
Nanostructures/chemistry , Photochemical Processes , Tin Compounds/chemistry , Zinc Oxide/chemistry , Catalysis , Spectrophotometry, Ultraviolet , Surface Properties , X-Ray DiffractionABSTRACT
Palladium in automotive exhaust catalyst was determined by flame atomic absorption spectrometry (FAAS). The analytical conditions and the coexisting elements interference were studied. The catalyst was dissolved by the mixture of H2O2 and HCl. Pd in the solution was directly determined by FAAS method. The linearity of working curve ranges from 0.1 to 15 microg x mL(-1); the detection limit is 0.029 microg x mL(-1); the relative standard deviation (RSD) range is from 0.8% to 2.5%; and the recovery rate range is from 99.6% to 101.2%. It is a simple and convenient method for accurate analysis of Pd in the exhaust catalysts.
ABSTRACT
Single-crystal V2O5 nanowires were successfully synthesized from the starting materials V6O13 powder and water. The experimental results indicate that high purity nanowires can be obtained using this simple synthetic route in absence of templates or catalysts. The diameter of the nanowires was found to be ca. 20 approximately 60 nm and the length up to several tens of micrometers, and the phases of nanowires were determined by XRD and TEM measurements.
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Brookite-type TiO(2) nanotubes with crystalline multilayer walls have been synthesized for the first time via a simple hydrothermal route.
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Low-dimensional ZnO nanocrystals with controlled size, aspect ratio, and oxygen defects (e.g., type and concentration) are successfully prepared through simple solvothermal and thermal treatment methods. The structure of the as-synthesized samples is characterized by XRD, N2 physical adsorption, TEM, and IR and XPS spectra. The results show that the aspect ratio and size of the as-synthesized ZnO nanocrystals increase with increasing [OH-]/[Zn2+]; the morphology evolves from nanorod to nanoparticle with an increase in the annealing temperature; the BET surface areas of the corresponding samples decrease during these processes, respectively; and different oxygen defects, which are likely to be oxygen vacancy (Vo**) and interstitial oxygen (Oi''), are formed in our experiments accordingly. With evolution of the structure, IR absorption bands and visible photoluminescence emission peaks of the synthesized ZnO nanocrystals shift and split, which is ascribed to the change of oxygen defects. In addition, it is found that the photocatalytic activity of the synthesized ZnO nanocrystals is mainly dependent on the type and concentration of oxygen defects. The relationship of structure-property and the possible photocatalytic mechanism are discussed in detail.
ABSTRACT
A high yield of the dimer-type heterostructure of Ag/ZnO nanocrystals with different Ag contents is successfully prepared through a simple solvothermal method in the absence of surfactants. The samples are characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-vis spectroscopy, and IR spectroscopy. The results show that all samples are composed of metallic Ag and ZnO; Ag nanoparticles locate on the surface of ZnO nanorods; the binding energy of Ag 3d(5/2) for the Ag/ZnO sample with a Ag content of 5.0 atom % shifts remarkably to the lower binding energy compared with the corresponding value of pure metallic Ag because of the interaction between Ag and ZnO nanocrystals; the concentration of oxygen vacancy for the as-synthesized samples varies with the increasing Ag content, and the Ag/ZnO sample with a Ag content of 5.0 atom % has the largest density of oxygen vacancy. In addition, the relationship between their structure and photocatalytic property is investigated in detail. It is found that the photocatalytic property is closely related to its structure, such as heterostructure, oxygen defect, and crystallinity. The presence of metallic Ag nanoparticles and oxygen vacancy on the surface of ZnO nanorods promotes the separation of photogenerated electron-hole pairs and thus enhances the photocatalytic activity.
ABSTRACT
Heating reflux aging technology was first applied to obtain a series of ceria zirconia mixed oxides composed of 0.6CeO2-0.4ZrO2. N2 physical adsorption, FT-Raman, and UV-Vis diffuse spectroscopy techniques were preformed to investigate the relationships between the structure and oxygen storage capacity of ceria zirconia mixed oxides prepared at different pH value of precipitation. The composition of ceria zirconia mixed oxides fluctuated with the pH value of precipitation, leading to the variation in phase ingredients, defects, crystallization and texture. Controlling the pH value of precipitation at 10.5-11.0 can avoid the introduction of Si, improve the texture, phase homogeneity and defects concentration, decrease the degree of crystallization, and increase the oxygen storage capacity.
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Heating reflux aging technology was applied to prepare a series of Ce(x)Zr(1-x)O2 (0.25 < or = x < or = 1) solid solution. The effects of the Ce(x)Zr(1-X)O2 composition on the structure and oxygen storage capacity were characterized using N2 physical adsorp tion, X-ray diffraction (XRD), FT-Raman, UV-Vis diffuse spectroscopy techniques. The texture, structure and thermal stability of ceria-zirconia mixed oxides are closely related to the ratio of cerium to zirconium in the solid solution, with increasing the zirconium content, the specific area increases, and the structure undergoes a change of order --> disorder --> order. Among them, Ce(0.4Zr(0.6)O2 sample possesses the maximum OSC and Ce(0.25)Zr(0.75)O2 sample possesses the best thermal stability.
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A variety of synthesis parameters for the preparation of gold nanoparticles by NaBH4 solution reduction in the W/O microemulsion media consisting of Cetyl Trimethyl Ammonium Bromide (CTAB)/n-hexanol/water system was investigated. The results showed that the molar ratio of water to surfactant (rw) had nothing to do with the gold particle size, but the concentration of the aqueous gold salt solution had a significant effect on the size of gold particle. Through optimizing the preparation parameters, Au/Al2O3 catalysts were prepared with two different methods, then the catalysts were characterized by ultraviolet-visible spectra, XRD and TEM, and the effect of two different preparation methods on active component gold particle size in the catalysts was studied.
ABSTRACT
Diffusion Reflectance Spectroscopy (DRS) was employed to study the surface phase structure of ZrO2-based catalysts. The effect of calcining temperature, and the addition of Al2O3 and platinum on the surface and bulk phase structures of zirconia was studied by DRS combined with XRD, DTA and XPS. The same trend was observed that heating to higher temperatures results in the conversion to monoclinic zirconia in undoped samples, while incorporation of an appropriate amount of Al2O3 would stabilize the tetragonal phase zirconia. And the reduction processing of Pt/ZrO2 affects crystallization and phase transitions, resulting in certain fraction of tetragonal ZrO2 transferred to monoclinic ZrO2. The DRS shows an appreciable difference in the corresponding XRD spectra that more monoclinic zirconia formed on the surface of catalyst during the reduction processing of Pt/ZrO2, compared to the bulk of catalyst.
