Biocompatible nanostructured high-velocity oxyfuel sprayed titania coating: Deposition, characterization, and mechanical properties

Nanostructured titania (TiO₂) coatings were produced by high-velocity oxyfuel (HVOF) spraying. They were engineered as a possible candidate to replace hydroxyapatite (HA) coatings produced by thermal spray on implants. The HVOF sprayed nanostructured titania coatings exhibited mechanical properties, such as hardness and bond strength, much superior to those of HA thermal spray coatings. In addition to these characteristics, the surface of the nanostructured coatings exhibited regions with nanotextured features originating from the semimolten nanostructured feedstock particles. It is hypothesized that these regions may enhance osteoblast adhesion on the coating by creating a better interaction with adhesion proteins, such as fibronectin, which exhibit dimensions in the order of nanometers. Preliminary osteoblast cell culture demonstrated that this type of HVOF sprayed nanostructured titania coating supported osteoblast cell growth and did not negatively affect cell viability. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Suspension plasma spraying of nanostructured WC-12Co coatings

Nanostructured WC-12% Co coatings were deposited by suspension plasma spraying of submicron feedstock powders, using an internal injection plasma torch. The liquid carrier used in this approach allows for controlled injection of much finer particles than in conventional thermal spraying, leading to thin coatings with a fine surface finish. A polyethylene-imine (PEI) dispersant was used to stabilize the colloidal suspension in an ethanol carrier. In-flight particle states were measured for a number of operating conditions of varying plasma gas flow rates, feed rates, and standoff distances and were related to the resulting microstructure, phase composition (EDS, SEM, XRD), and Vickers hardness. High in-flight particle velocities (>800 m/s) were generated, leading to dense coatings. It was observed that the coating quality was generally compromised by the high temperature and reactivity of the small particles. To compensate for this shortcoming, the suspension feed rate was adjusted, thereby varying the thermal load on the plasma. Results showed that a slightly larger agglomerate size, in conjunction with low particle jet temperatures, could somewhat limit the decomposition of WC into brittle W₂C/W₃C and amorphous cobalt containing binder phases. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Comparison of the photocatalytic behavior of TiO2 coatings elaborated by different thermal spraying processes

This paper proposes a comparative study on the microstructure and photocatalytic performances of titanium dioxide coatings elaborated by various thermal spraying methods (plasma spraying in atmospheric conditions, suspension plasma spraying, and high-velocity oxyfuel spraying). Agglomerated spray dried anatase TiO₂ powder was used as feedstock material for spraying. Morphology and microstructural characteristics of the coatings were studied mainly by scanning electron microscopy and x-ray diffraction. The photocatalytic behavior of the TiO₂-base surfaces was evaluated from the conversion rate of gaseous nitrogen oxides (NOx). It was found that the crystalline structure depended strongly on the technique of thermal spraying deposition. Moreover, a high amount of anatase was suitable for the photocatalytic degradation of the pollutants. Suspension plasma spraying has allowed retention of the original anatase phase and for very reactive TiO₂ surfaces to be obtained for the removal of nitrogen oxides. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Protection of Ti6Al4V surfaces by laser dispersion of diborides

In this work, one- and two-step laser dispersing of Ti6Al4V surfaces by use of elemental boron (B) as well as TiB₂, ZrB₂, and CrB₂ was carried out with CO₂ and Nd:YAG lasers using an adapted apparatus to provide inert conditions. Depending on the laser system, melt pool depths between 200 μm and more than 1000 μm were achieved, and the boride precipitates allowed an increase of the surface hardness from 350 HV_0.05 in the initial state to more than 600 HV_0.05. The modified surface areas were characterized by means of optical microscopy, scanning electron microscopy, and EDXS. Oscillating and cavitation erosion wear tests were carried out. For reinforcement of component surfaces with complex shape, a two-step laser deposition process and a technology for predeposition of diboride layers with defined thickness is required. The applicability of vacuum plasma spraying for predeposition is discussed. The original version of this article was published as part of the ASM Proceedings, Thermal Spray 2003: Advancing the Science and Applying the Technology, International Thermal Spray Conference (Orlando, FL), May 5–8, 2003, Basil R. Marple and Christian Moreau, Ed., ASM International, 2003.     

Characterization of microstructure of Nano-TiO2 coating deposited by vacuum cold spraying

Control of the microstructure of TiO₂ coatings through preparation methods significantly influences the coating performance. In this study, a vacuum cold-spray process, as a new coating technology, is used to deposit nanocrystalline TiO₂ coatings on conducting glass and stainless steel substrates. TiO₂ deposits were formed using two types of nanocrystalline TiO₂ powders with mean particle diameters of 200 and 25 nm. Coating microstructures were characterized by scanning electron microscopy and x-ray diffraction analysis. Results demonstrate that a thick nanocrystalline TiO₂ coating can be deposited by the vacuum cold-spray process. The coating was found to consist of particles stacked as agglomerates that build up to several hundred nanometers. The coating also presents a mesoporous microstructure that could be effective in such applications as photocatalytic degradation and dye-sensitized solar cells. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

复合热源喷涂NiCr-Cr3C2涂层及其性能分析

采用激光与等离子复合热源喷涂技术,在38CrMoA1基体上制备NiCr-Cr3C2涂层,对涂层的结合强度、显微硬度、微观组织结构以及抗高温滑动摩擦磨损性能等进行了测试分析.结果表明,与传统的等离子喷涂层相比,复合热源喷涂时,NiCr-Cr2C2粉末受热熔融更充分,流动性好,铺展均匀.涂层实现了冶金结合,具有更高的结合强...     

Effect of Cu2+ doping on photocatalytic performance of liquid flame sprayed TiO2 coatings

Cu²⁺ was added to liquid feedstock to deposit ion doping TiO₂ photocatalytic coatings through liquid flame spraying. The coating microstructure was characterized by x-ray diffraction (XRD), transmission electron microscopy, and x-ray photoelectron spectroscopy (XPS). The photocatalytic performance of coatings was examined by photodegradation of acetaldehyde. The XRD analysis shows that the crystalline structure of coatings is not significantly influenced by Cu²⁺ doping. The photocatalytic activity of the TiO₂ coatings is enhanced by Cu²⁺ doping. It is found that a high concentration of Cu²⁺ doping decreases the activity. The XPS analysis shows that the adsorbed oxygen concentration is increased with the increase of Cu²⁺ dopant concentration and decreases with a further increase of dopant concentration. The enhancement of photocatalytic activity can be attributed to the adsorption ability of oxygen and other reactants on the surface of doping TiO₂ coatings. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Nanostructured photocatalytic titania coatings formed by suspension plasma spraying

This paper describes formation of titanium dioxide coatings designed for photocatalytic applications, obtained by suspension plasma spraying (SPS), an alternative of the atmospheric plasma spraying (APS) technique in which the material feedstock is a suspension of the material to be sprayed. Two different TiO₂ powders were dispersed in distilled water and ethanol and injected in Ar-H₂ or Ar-H₂-He plasma under atmospheric conditions. Scanning electron microscopy (SEM) and x-ray diffraction (XRD) analyses were performed to study the microstructure of the titania coatings. Photocatalytic efficiency of the elaborated samples was evaluated from the conversion ratio of different air pollutants: nitrogen oxides (NOx) and sulfur dioxide (SO₂). The morphology and crystalline structure of the deposits depended mainly on the nature of the solvent (water or alcohol) used in the preparation of the slurries. Dense coatings were obtained starting from aqueous suspensions and porous deposits were elaborated by plasma spraying of a PC105 alcoholic suspension. A significant phase transformation from anatase to rutile occurred when ethanol was used as a solvent. Different photocatalytic performances were observed as a function of the nature of the liquid material feed-stock, the spraying parameters, and the nature of the pollutant. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Characterization of YSZ solid oxide fuel cells electrolyte deposited by atmospheric plasma spraying and low pressure plasma spraying

Yttria doped zirconia has been widely used as electrolyte materials for solid oxide fuel cells (SOFC). Plasma spraying is a cost-effective process to deposit YSZ electrolyte. In this study, the 8 mol% Y₂O₃ stabilized ZrO₂ (YSZ) layer was deposited by low pressure plasma spraying (LPPS) and atmospheric plasma spraying (APS) with fused-crushed and agglomerated powders to examine the effect of spray method and particle size on the electrical conductivity and gas permeability of YSZ coating. The microstructure of YSZ coating was characterized by scanning electron microscopy and x-ray diffraction analysis. The results showed that the gas permeability was significantly influenced by powder structure. The gas permeability of YSZ coating deposited by fused-crushed powder is one order lower in magnitude than that by agglomerated powder. Moreover, the gas permeability of YSZ deposited by LPPS is lower than that of APS YSZ. The electrical conductivity of the deposits through thickness direction was measured by potentiostat/galvanostat based on three-electrode assembly approach. The electrical conductivity of YSZ coating deposited by low pressure plasma spraying with fused-crushed powder of small particle size was 0.043 S cm⁻¹ at 100 °C, which is about 20% higher than that of atmospheric plasma spraying YSZ with the same powder. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Influence of surface character change of substrate due to heating on flattening behavior of thermal sprayed particles

The authors have confirmed that in the thermal spraying of practical powder materials, the splat shape changes with increasing substrate temperature to a circular disk shape from a fringe shape with splashing at a critical substrate temperature,T _t. The increase of the substrate temperature may accompany a kind of essential change on the substrate surface, because the effect is maintained until the substrate is cooled down to room temperature. However, the nature of the substrate surface change due to the heating has not been clearly understood yet. In this study, AISI 304 stainless steel was used as a substrate material, and the substrate was heated in an air at mosphere or laser treated as a pretreatment. Substrate surface topography in nanometer scale was analyzed precisely by atomic force microscope (AFM). The relationship between surface topography in nanometer scale and splat morphology was discussed. Moreover, to evaluate the effect of chemical composition of the substrate surface, gold was coated onto the substrate surface by physical vapor deposition (PVD) after the heat treatment. The effect of adsorbate/condensate on the substrate surface on the flattening behavior of thermal sprayed particles was also verified. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Plasma spray synthesis from precursors: Progress, issues, and considerations

Precursor plasma spray synthesis is an innovative and rapid method for making functional oxide ceramic coatings by starting from solution precursors and directly producing inorganic films. This emerging method utilizes molecularly mixed precursor liquids, which essentially avoids the handling and selection of powders, opening up new avenues for developing compositionally complex functional oxide coatings. Precursor plasma spray also offers excellent opportunities for exploring the nonequilibrium phase evolution during plasma spraying of multicomponent oxides from inorganic precursors. Although there have been efforts in this area since the 1980s and early 1990s with the goal of synthesizing nanoparticles, only recently has the work progressed in the area of functional systems. At the Center for Thermal Spray Research an integrated investigative strategy has been used to explore the benefits and limits of this synthesis strategy. Water- and alcohol-based sol/solution precursors derived from various chemical synthesis methods were used as feedstocks to deposit thin/thick films of spherical and nanostructured coatings of yttrium aluminum garnet (YAG), yttrium iron garnet, lanthanum strontium manganate and Zr-substituted yttrium titanates, and compositions of Y₂O₃-Al₂O₃ and their microstructural space centered around stoichiometric YAG. A detailed discussion of the salient features of the radiofrequency induction plasma spraying approach, the results obtained in the investigations to develop various functional oxide coatings, and process issues and challenges are presented. This article was originally published inBuilding on 100 Years of Success: Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Characterizations and hot corrosion resistance of Cr3C2-NiCr coating on Ni-base superalloys in an aggressive environment

In the current study, Cr₃C₂-NiCr coating was deposited on the Ni-base superalloys by using high velocity oxyfuel (HVOF) process for high temperature corrosive environment applications. Optical microscopy (OM), x-ray diffraction (XRD), scanning electron microscopy/energy-dispersive analysis (SEM/EDAX), microhardness tester, and electro probe microanalyzer (EMPA) techniques were used to characterize the coating with regard to coating thickness, porosity, microhardness, and microstructure. The thermogravimetric technique was used to establish kinetics of corrosion. The hot corrosion behaviors of the bare and Cr₃C₂-NiCr coated superalloys were studied after exposure to aggressive environment of Na₂SO₄-60% V₂O₅ salt mixture at 900 °C under cyclic conditions. The structure of the as-sprayed Cr₃C₂-NiCr coating mainly consisted of γ-nickel solid solution along with minor phases of Cr₇C₃ and Cr₂O₃. Coating has porosity less than 1.5% and microhardness in the range of 850–900 Hv (Vickers hardness). Some inclusions, unmelted and semimelted powder particles were observed in the structure of the coatings. The Cr₃C₂-NiCr coating has imparted necessary resistance to hot corrosion, which has been attributed to the formation of oxides of nickel and chromium, and spinel of nickel-chromium. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

High-velocity DC-VPS for diffusion and protecting barrier layers in solid oxide fuel cells (SOFCs)

High-temperature fuel cells of the solid oxide fuel cell (SOFC) type as direct converter of chemical into electrical energy show a high potential for reducing considerably the specific energy consumption in different application fields. Of particular interest are advanced lightweight planar cells for electricity supply units in cars and other mobile systems. Such cells, in one new design, consist mainly of metallic parts, for example, of ferrite steels. These cells shall operate in the temperature range of 700 to 800 °C where oxidation and diffusion processes can be of detrimental effect on cell performance for long-term operation. Problems arise in particular by diffusion of chromium species from the interconnect or the cell containment into the electrolyte/cathode interface forming insulating phases and by the mutual diffusion of substrate and anode material, for example, iron and chromium from the ferrite into the anode and nickel from the anode into the ferrite, which in both cases reduces performance and system lifetime. Additional intermediate layers of perovskite-type material, (e.g., doped LaCrO₃) applied with high-velocity direct-current vacuum plasma spraying (DC-VPS) can reduce such effects considerably if they are stable and of high electronic conductivity. This article was originally published inBuilding on 100 Years of Success, Proceedings of the 2006 International Thermal Spray Conference (Seattle, WA), May 15–18, 2006, B.R. Marple, M.M. Hyland, Y.-Ch. Lau, R.S. Lima, and J. Voyer, Ed., ASM International, Materials Park, OH, 2006.     

Study of Al2O3 coatings on AISI 316 stainless steel obtained by controlled atmosphere plasma spraying (CAPS)

The tribological behaviour of Al₂O₃ coatings on AISI 316 stainless steel, obtained by the process of controlled atmosphere plasma spraying (CAPS), is studied in this work. Atmospheric plasma spraying (APS) and high pressure plasma spraying (HPPS) were applied in order to produce these coatings. The APS coatings exhibited lower microhardness values compared to the values of HPPS coatings. Regarding the HPPS coatings it was found that plasma composition, through its heat capacity, does influence the heat transfer to particles, and, consequently, their flattening and densification process, which govern coating properties. It was revealed that tribological behaviour of coatings was influenced by the applied spraying method too. Coatings from HPPS under high-enthalpy conditions led to worst wear behaviour. In general, properties, such as microstructure, microhardness, coefficient of friction and wear resistance depended on the processing conditions such as pressure and composition of the spraying chamber atmosphere.     

Fabrication of Nano-TiO2 Coating for Dye-Sensitized Solar Cell by Vacuum Cold Spraying at Room Temperature

Deposition of nanocrystalline TiO₂ coating at low temperature is becoming more attractive due to the possibility for continuous roll production of the coating for assembly lines of dye-sensitized solar cell (DSC) at a low cost. In this study, porous nano-TiO₂ coating was deposited by vacuum cold spraying (VCS) at room temperature on a conducting glass substrate using commercial P25 nanocrystalline TiO₂ powder. The microstructure of TiO₂ coating was characterized by field emission scanning electron microscopy (FESEM) and nitrogen adsorption test. A commercial dye (N719) was adsorbed on the surface of TiO₂ particles within the coating to assemble a DSC. The cell performance was evaluated by employing simulated solar light at an intensity of 100 mW/cm². The results showed that TiO₂ coating was deposited by the agglomerates of nano-TiO₂ powders. The Brunauer-Emmett-Teller (BET) test of the as-sprayed TiO₂ coating yielded a porosity of 49% and an average pore size of 17 nm. The assembled solar cell yielded a short-circuit current density of 7.3 mA/cm² and an energy conversion efficiency of 2.4%. The test results indicate that VCS was a promising method to deposit nanocrystalline TiO₂ coatings at low temperature applied to DSCs. This article is an invited paper selected from presentations at the 2007 International Thermal Spray Conference and has been expanded from the original presentation. It is simultaneously published in Global Coating Solutions, Proceedings of the 2007 International Thermal Spray Conference, Beijing, China, May 14-16, 2007, Basil R. Marple, Margaret M. Hyland, Yuk-Chiu Lau, Chang-Jiu Li, Rogerio S. Lima, and Ghislain Montavon, Ed., ASM International, Materials Park, OH, 2007.     

Plasma spray coating of spray-dried Cr2O3/wt.% TiO2 powder

An agglomerated Cr₂O₃/wt.%TiO₂ powder has been fabricated by the spray drying process under different parameters. The spray-dried powder has well-agglomerated particles of spherical shape. In the conditions of the high slurry feed rate and low binder concentration in the slurry, the powder has large cavities inside some particles and ruggedness over their surface. The optimum plasma spray feed rate has been found by examining the spraying behavior of the powder and melted state of particles. The plasma spray coating has been performed under different process variables such as spraying distance and plasma power. These parameters strongly affect the characteristics of the coated layer: microstructure, hardness, and bond strength.     

Microstructural Analysis and Photocatalytic Activity of Plasma-Sprayed Titania-Hydroxyapatite Coatings

Hydroxyapatite (HAp Ca₁₀(PO₄)₆(OH)₂) is known to be a biomaterial and an adsorbent for chromatography. In this study, HAp was agglomerated with anatase TiO₂ to manufacture thermal-spray powders to improve the adsorption activity of TiO₂, and then to improve its photocatalytic activity. The microstructures, compositions and photocatalytic activity of plasma-sprayed TiO₂, TiO₂-10%HAp, TiO₂-30%HAp, and HAp coatings were investigated. Due to the low thermal conductivity of HAp compound, not all HAp particles fully melted even under the arc current of 800 A. The addition of HAp inhibited the phase transformation of anatase TiO₂ to rutile. Under the arc current of 600 A, the anatase content in the TiO₂, TiO₂-10%HAp and TiO₂-30%HAp coatings was 11, 20 and 42%, respectively. With the increasing of the spraying distance from 70 to 110 mm, the anatase content in the TiO₂-30%HAp coatings decreased from 34 to 17% under arc current of 700 A. Furthermore, a slight decomposition of HAp to α-Ca₃(PO₄)₂ was found in the TiO₂-30%HAp coatings, it did not decompose to CaO and P₂O₅ according to the XRD and EDAX analysis. The addition of the secondary gas of helium had no significant influence on the melting state of the TiO₂-HAp feedstock powders. Moreover, the HAp in the TiO₂-10%HAp and TiO₂-30%HAp coatings had adsorption characteristic to acetaldehyde. The photocatalytic activity of TiO₂-10%HAp coating was highest among TiO₂, TiO₂-10%HAp, and TiO₂-30%HAp coatings sprayed under the arc current of 600 A for the optimum adsorption property and anatase content. This article is an invited paper selected from presentations at the 2007 International Thermal Spray Conference and has been expanded from the original presentation. It is simultaneously published in Global Coating Solutions, Proceedings of the 2007 International Thermal Spray Conference, Beijing, China, May 14-16, 2007, Basil R. Marple, Margaret M. Hyland, Yuk-Chiu Lau, Chang-Jiu Li, Rogerio S. Lima, and Ghislain Montavon, Ed., ASM International, Materials Park, OH, 2007.     

Relation Between the Arc-Root Fluctuations, the Cold Boundary Layer Thickness and the Particle Thermal Treatment

In plasma spraying, the arc-root fluctuations, modifying the length and characteristics of the plasma jet, have an important influence on particle thermal treatment. These voltage fluctuations are strongly linked to the thickness of the cold boundary layer (CBL), surrounding the arc column. This thickness depends on the plasma spray parameters (composition and plasma forming gas mass flow rate, arc current, etc.) and the plasma torch design (anode-nozzle internal diameter and shape, etc.). In order to determine the influence of these different spray parameters on the CBL properties and voltage fluctuations, experiments were performed with two different plasma torches from Sulzer Metco. The first one is a PTF4 torch with a cylindrical anode-nozzle, working with Ar-H₂ plasma gas mixtures and the second one is a 3MB torch with either a conical or a cylindrical anode-nozzle, working with N₂-H₂ plasma gas mixtures. Moreover, arc voltage fluctuations influence on particle thermal treatment was studied through the measurements of transient temperature and velocity of particles, issued from an yttria partially stabilized zirconia powder with a size distribution between 5 and 25 μm. This article is an invited paper selected from presentations at the 2007 International Thermal Spray Conference and has been expanded from the original presentation. It is simultaneously published in Global Coating Solutions, Proceedings of the 2007 International Thermal Spray Conference, Beijing, China, May 14-16, 2007, Basil R. Marple, Margaret M. Hyland, Yuk-Chiu Lau, Chang-Jiu Li, Rogerio S. Lima, and Ghislain Montavon, Ed., ASM International, Materials Park, OH, 2007.     

Microstructure evolution during reactive plasma spraying of MoSi2 with methane

The mechanisms that govern microstructure evolution during reactive plasma spraying of MoSiz using 100% methane were investigated, with particular emphasis on the thermodynamics and kinetics of the relevant phase transformations and chemical reactions. The reactive plasma-sprayed M0Si₂ exhibited a dense, multilayered microstructure. In addition to the M0Si₂ matrix, significant amounts of M0₅Si₃ and elemental carbon were observed, along with a small amount of SiC. Thermodynamic and kinetic analysis predicted a large volume fraction of M0₅Si₃ and a small amount of SiC in the as-deposited reactive plasma-sprayed MoSi₂, in agreement with the experimental observations.     

Synthesis of CeO2/TiO2 nanoparticles by laser ablation of Ti target in cerium (III) nitrate hexahydrate (Ce(NO3)3·6H2O) aqueous solution

A new synthesis process, laser ablation in an aqueous solution of target material, was applied to synthesize nanostructured CeO₂/TiO₂ catalyst particles. Reactivity within the laser plume (plasma) can be used to synthesize CeO₂ from an aqueous solution, 2 M cerium (III) nitrate hexahydrate (Ce(NO₃)₃·6H₂O) aqueous solution, and to fabricate TiO₂ from Ti target. CeO₂/TiO₂ nanoparticles were successfully synthesized by the laser ablation of Ti target in 2 M cerium (III) nitrate hexahydrate (Ce(NO₃)₃·6H₂O) aqueous solution. Laser ablation of Ti in a liquid environment and chemical reactions of the solution within a plasma plume are discussed.