Patent Application
20150240151
The present disclosure relates to luminescent materials, and more particularly relates to a zinc aluminate luminescent material and a preparation method thereof.
Field emission display (FED) is a flat panel display technology having a great development potential. While the operating voltage of field emission display device is lower than that of the cathode ray tube (CRT), the operating current density of FED is relatively larger, e.g., about 10 to 100 μA·cm−2. Accordingly, the fluorescent material for the field emission display requires a higher demand, such as better chromaticity, higher luminous efficiency at low voltage, and no brightness saturation phenomena at high current densities.
Currently, the study on FED mainly focuses on two aspects: one is to use and modify the existing fluorescent material for CRT; another is to search for new fluorescent material. The commercial available fluorescent material for CRT is usually based on sulfide, however, when it is used for manufacturing FED, sulfur may reacts with trace molybdenum, silicon or germanium contained in the cathode due to the instability of sulfides, which weakens the electron emission, resulting a weak FED luminous intensity.
Accordingly, it is necessary to address the problem of low luminous intensity of the conventional luminescent materials and to provide a zinc aluminate luminescent material having a higher luminous intensity and preparation method thereof.
A zinc aluminate luminescent material has a general molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My,
wherein A is selected from the group consisting of Cr, Eu, Tb, and Ce;
M is at least one metal nanoparticles selected from the group consisting of Ag, Au, Pt, Pd, and Cu;
0<x≦0.1;
y is a molar ratio between M and the sum of the molar mass of Al in Zn1-xAl2O4:A3+x and Al in Al2O3@My, 0<y≦1×10−2;
@ represents coating; the zinc aluminate luminescent material uses M as a core, Al2O3 as an inner shell, and Zn1-xAl2O4:A3+x as an outer shell.
In one embodiment, 0.0005≦x≦0.05.
In one embodiment, 1×10−5≦y≦5×10−3.
A method of preparing a zinc aluminate luminescent material includes the following steps:
preparing a sol containing M, wherein M is at least one metal nanoparticles selected from the group consisting of Ag, Au, Pt, Pd and Cu;
surface-treating the sol containing M, adding a solution containing Al3+, stirring, adding a precipitating agent, reacting at a temperature ranging from 0° C. to 100° C. to form a precipitate, filtering, washing, drying, and calcining the precipitate to obtain Al2O3 powder coating M;
mixing compounds containing Zn and A, and the Al2O3 powder coating M according to a stoichiometry ratio in a molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My to obtain a mixture, wherein A is selected from the group consisting of Cr, Eu, Tb, and Ce; 0<x≦0.1; y is a ratio between the molar amount of M and a sum of the molar amount of Al in Zn1-xAl2O4:A3+x and Al in Al2O3@My, 0<y≦1×10−2; and
grinding and mixing the mixture, calcining the mixture, cooling and grinding to obtain the zinc aluminate luminescent material having a general molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My, wherein @ represents coating; the zinc aluminate luminescent material uses M as a core, Al2O3 as an inner shell, and Zn1-xAl2O4:A3+x as an outer shell.
In one embodiment, the preparing the sol containing M includes:
mixing and reacting a salt solution of at least one of Ag, Au, Pt, Pd, and Cu, an additive, and a reducing agent for 10 minutes to 5 minutes to obtain the sol containing M nanoparticles;
a concentration of the salt solution of at least one of Ag, Au, Pt, Pd, and Cu ranges from 1×10−3 mol/L to 5×10−2 mol/L;
the additive is at least one selected from the group consisting of polyvinyl pyrrolidone, sodium citrate, cetyl trimethyl ammonium bromide, sodium lauryl sulfate, and sodium dodecyl sulfate;
a concentration of additive in the sol containing M ranges from 1×10−4 g/mL to 5×10−2 g/mL;
the reducing agent is at least one selected from the group consisting of hydrazine hydrate, ascorbic acid, sodium citrate, and sodium borohydride;
a molar ratio of the reducing agent to a metal ion in the salt solution of at least one of Ag, Au, Pt, Pd, and Cu ranges from 3.6:1 to 18:1.
In one embodiment, the surface-treating the sol containing M includes:
adding the sol containing M to a polyvinyl pyrrolidone aqueous solution having a concentration of 0.005 g/mL to 0.1 g/mL and stirring for 12 to 24 hours.
In one embodiment, the method further includes: adding a surfactant prior to the adding of the precipitating agent and after stirring.
In one embodiment, the solution containing Al3+ is selected from the group consisting of aluminum sulfate solution, aluminum nitrate solution, and aluminum chloride solution; the surfactant is selected from the group consisting of polyethylene glycol, ethylene glycol, isopropyl alcohol, and polyvinyl alcohol; the precipitating agent is selected from the group consisting of ammonium bicarbonate, ammonia, ammonium carbonate, and urea.
In one embodiment, the method further includes: aging for 2 hours to 12 hours prior to the filtering and after the forming the precipitate.
In one embodiment, the calcining the precipitate to obtain Al2O3 powder coating M includes: calcining the precipitate at a temperature of 500° C. to 1200° C. for 1 hour to 8 hours.
In one embodiment, the calcining the ground mixture includes: calcining the mixture at a temperature of 800° C. to 1400° C. for 2 hours to 15 hours, then calcining the mixture at a temperature of 1000° C. to 1400° C. for 0.5 hour to 6 hours under a mixed reducing atmosphere of nitrogen and hydrogen, a reducing atmosphere of carbon or a reducing atmosphere of hydrogen.
The zinc aluminate luminescent material uses at least one metal nanoparticles Ag, Au, Pt, Pd, and Cu as the core, Al2O3 as the inner shell, and Zn1-xAl2O4:A3+x as the outer shell, thus forming a core-shell structure. The metal nanoparticles can improve the internal quantum efficiency of the luminescent material, such that the luminous intensity of the zinc aluminate luminescent material is increased.
Reference will now be made to the drawings to describe, in detail, embodiments of the present zinc aluminate luminescent material and preparation method thereof.
An embodiment of a zinc aluminate luminescent material is provided having a general molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My,
wherein A is selected from the group consisting of chromium (Cr), europium (Eu), terbium (Tb), and cerium (Ce);
M is at least one metal nanoparticles selected from the group consisting of silver (Ag), gold (Au), platinum (Pt), palladium (Pd) and copper (Cu);
0<x≦0.1; preferably 0.0005≦x≦0.05.
y is a molar ratio between M and the sum of the molar mass of Al in Zn1-xAl2O4:A3+x and Al in Al2O3@My, 0<y≦1×10−2; preferably 1×10−5≦y≦5×10−3;
@ represents coating; the zinc aluminate luminescent material uses M as a core, Al2O3 as an inner shell, and Zn1-xAl2O4:A3+x as an outer shell.
In the general molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My, “:” represents doping, i.e. ZnAl2O4 serves as a luminescent substrate, A serves as the doping element, and trivalent A ion is an activate ion of the luminescent material. The outer shell of Zn1-xAl2O4:A3+x is formed by doping A into the ZnAl2O4 and replacing partial Zn in the ZnAl2O4.
Zinc aluminate (ZnAl2O4) is a kind of wide band gap semiconductor material having a cubic spinel structure. The optical, band gap of ZnAl2O4 polycrystalline powder is generally about 318 to 319 eV, thus it has excellent chemical and thermal stability. Since the aluminum zinc analogues Zn1-xAl2O4 is used as the substrate material of the outer shell, the zinc aluminate luminescent material exhibits a high stability.
Since M serves as a core of the zinc aluminate luminescent material, it can cause the surface plasmon resonance effect, so as to improve the internal quantum efficiency of the zinc aluminate luminescent material.
The zinc aluminate luminescent material uses at least one metal nanoparticles Ag, Au, Pt, Pd, and Cu as the core, Al2O3 as the inner shell, and Zn1-xAl2O4:A3+x as the outer shell, thus forming a core-shell structure. The metal nanoparticles can improve the internal quantum efficiency of the luminescent material, such that the luminous intensity of the zinc aluminate luminescent material is increased.
This zinc aluminate luminescent material has such advantages as good stability, good luminous performance, thus it can be widely applied in the field of display and lighting applications.
Comparing to the conventional sulfide luminescent materials, this zinc aluminate luminescent material does not produce toxic sulfide during use, thus it is environmentally friendly, non-toxic, and safe to use.
A method of preparing a zinc aluminate luminescent material includes the following steps:
In step S110, a sol containing M is prepared.
M is at least one metal nanoparticles selected from the group consisting of Ag, Au, Pt, Pd, and Cu.
The step of preparing the sol containing M includes: mixing and reacting a salt solution of at least one of Ag, Au, Pt, Pd, and Cu, an additive, and a reducing agent to obtain the sol containing M nanoparticles. In order to guarantee that the sol containing M is obtained, the reaction time is preferably ranged from 10 to 45 minutes to save energy.
The salt solution of Ag, Au, Pt, Pd, and Cu can be a chloride solution, a nitrate solution or the like of the Ag, Au, Pt, Pd, and Cu. The concentration of the salt solution of Ag, Au, Pt, Pd, and Cu can be determined according to the actual needs, preferably ranges from 1×10−3 mol/L to 5×10−2 mol/L.
The additive is at least one selected from the group consisting of polyvinyl pyrrolidone, sodium citrate, cetyl trimethyl ammonium bromide, sodium lauryl sulfate, and sodium dodecyl sulfate. The concentration of additive in the sol containing M ranges from 1×10−4 g/mL to 5×10−2 g/mL.
The reducing agent is at least one selected from the group consisting of hydrazine hydrate, ascorbic acid, sodium citrate, and sodium borohydride. The reducing agent is firstly formulated into an aqueous solution with a concentration of 1×10−4 mol/L to 1 mol/L, then is mixed and reacted with the salt solution of at least one of Ag, Au, Pt, Pd, and Cu, and the additive.
A molar ratio of the reducing agent to a metal ion in the salt solution of at least one of Ag, Au, Pt, Pd, and Cu ranges from 3.6:1 to 18:1.
Under the effect of the reducing agent and additives, Ag, Au, Pt, Pd or Cu ions are reduced to Ag, Au, Pt, Pd or Cu metal nanoparticles and dispersed in a solvent, such that the sol containing M is obtained.
In step S120, the sol containing M is surface-treated, a solution containing Al3+ is added, after stirring, a precipitating agent is added, the reaction is carried out at a temperature ranging from 0° C. to 100° C. to form a precipitate, the precipitate is filtered, washed, dried, and calcined to obtain Al2O3 powder coating M.
For ease of coating, the sol containing M obtained from the step S110 is firstly surface-treated to form a stable Al2O3 powder coating M, referred hereafter as Al2O3@M.
Specifically, the step of surface-treating the sol containing M includes: adding the sol containing M to a polyvinyl pyrrolidone (PVP) aqueous solution having a concentration of 0.005 g/ml to 0.1 g/ml and stirring for 12 to 24 hours.
The solution containing Al3+ is selected from the group consisting of aluminum sulfate solution (Al2(SO4)3), aluminum nitrate solution (Al(NO3)3), and aluminum chloride solution (AlCl3).
The precipitating agent is selected from the group consisting of ammonium bicarbonate (NH4HCO3), ammonia (NH3.H2O), ammonium carbonate ((NH4)2CO3), and urea (CON2H4).
The surface-treated sol containing M is added with the solution containing Al3+, after well stirring, the precipitating agent is added slowly with stirring, the reaction is carried out in a 0° C. to 100° C. water bath to form a precipitate. The reaction time is preferably from 1.5 hours to 5 hours to complete the generation of the precipitate.
Al3+ ion can react with the precipitating agent to produce Al(OH)3, which takes a form of colloid. Since the hydroxyls of Al(OH)3 have a high activity, the firstly generated Al(OH)3 colloid can bind metal and coat the metal inside, next, the subsequently generated Al(OH)3 will be deposited on the surface of the colloid particles. The hydroxyl bound to the surface of the colloid particle will be dehydrated and form an Al—O—Al band and binding points. Along with the hydrolysis, Al(OH)3 will continuously bind to the binding points, and an Al2O3 coating layer is formed by dehydration and condensation, such that Al2O3@M is obtained.
Preferably, prior to adding the precipitating agent and after stirring, a surfactant is added.
Before adding the surfactant, the sol containing M maintains stable mainly by electrostatic repulsion between particles. The added surfactant can be used to prevent agglomeration of the particles, thus further improving the stability of the particles.
The surfactant can form a molecular film on the surface of the colloid particles to prevent contacting between the particles, and the molecular film can reduce the surface tension and the capillary adsorption, and reduce the steric effect, such that the purpose of preventing agglomeration can be achieved. After the particle is bound with the surfactant, the bonding effect of —OH of the surface of the colloid particles can be reduced, thus further improving the dispersion of the colloid, and reducing the agglomeration of particles.
The surfactant is selected from the group consisting of polyethylene glycol (PEG), ethylene glycol (EG), isopropyl alcohol (IPA), and polyvinyl alcohol ([C2H4O]n). Preferably, the polyethylene glycol is polyethylene glycol 100-20000 (PEG 100-20000), more preferably polyethylene glycol 2000-10000 (PEG2000-10000).
The polyethylene glycol with a molecular weight of 2000 to 10000 has an appropriate viscosity, such that PEG2000-10000 can easily form a strong hydrogen bond with the surface of the particles, and a macromolecular hydrophilic film is formed on the surface of the particles, so that the dispersion particles is improved, and the aggregation of particles is reduced.
Preferably, after the reaction is completed, the precipitate is aged for 2 to 12 hours, such that the generated precipitated crystal particles can grow up, and the precipitate becomes more pure and is easy for separation.
After aging, the precipitate is obtained by filtering. The precipitate is then washed, dried, and calcined at a temperature of 500° C. to 1200° C. for 1 to 8 hours to obtain Al2O3 powder, which coats M.
In step S130, compounds containing Zn and A, and the Al2O3 powder coating M are mixed according to a stoichiometry ratio in a molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My to obtain a mixture, wherein A is selected from the group consisting of Cr, Eu, Tb, and Ce; 0<x≦0.1; y is a ratio between the molar amount of M and a sum of the molar amount of Al in Zn1-xAl2O4:A3+x and Al in Al2O3@My, 0<y≦1×1031 2.
The compounds containing Zn and A can be oxides, carbonates, acetates or oxalates corresponding to Zn and Mn. For example, the compounds containing Zn can be zinc oxide (ZnO), zinc oxalate (ZnC2O4.2H2O), and the like; the compounds containing A can be chromium oxalate hexahydrate (Cr2(C2O4)3.6H2O), Europium carbonate (Eu2(CO3)3), and the like.
The compounds containing Zn and A, and the Al2O3@M powder are mixed according to a stoichiometric ratio of formula of Zn1-xAl2O4:A3+x@Al2O3@My to obtain a mixture, which will be used for subsequent reaction.
In step S140, the mixture is ground, well mixed, calcined, cooled and ground again to obtain the zinc aluminate luminescent material having a general molecular formula of Zn1-xAl2O4:A3+x@Al2O3@My, wherein @ represents coating; the zinc aluminate luminescent material uses M as a core, Al2O3 as an inner shell, and Zn1-xAl2O4:A3+x as an outer shell.
The mixture obtained in step S130 is well ground, then is calcined at a temperature of 800° C. to 340O° C. for 2 to 15 hours. Next, the mixture is reduced under a mixed reducing atmosphere of nitrogen and hydrogen, a carbon reducing atmosphere or a hydrogen reducing atmosphere at a temperature of 1000° C. to 1400° C. for 0.5 to 6 hours.
The zinc aluminate luminescent material of Zn1-xAl2O4:A3+x@Al2O3@My is obtained by calcining, cooling, and grinding, in which @ represents coating; the zinc aluminate luminescent material uses M as a core, Al2O3 as an inner shell, and Zn1-xAl2O4:A3+x as an outer shell.
The grinding and mixing of the mixture of compounds containing Zn and A, and the Al2O3@M powder before calcining can enable a fully reaction. The mixture is calcined, cooled, and ground again to obtain the zinc aluminate luminescent material with a smaller particle size and more uniform particle size distribution.
The forgoing preparing method of the zinc aluminate luminescent material is simple, low equipment requirement, no pollution, easy to control, and suitable for industrial production.
Detailed examples are described below.
This example describes a process of preparation of Zn0.99Al2O4:Cr3+0.0005@Al2O3@Pd1×10−5 by using high-temperature solid-phase method.
Preparation of sol containing Pd nanoparticles was described below.
0.22 mg of palladium chloride (PdCl2.2H2O) was dissolved in 19 mL of deionized water. After the palladium chloride was fully dissolved, 11.0 mg of sodium citrate and 4.0 mg of sodium lauryl sulfate were weighed and dissolved into the palladium chloride aqueous solution under magnetic stirring. 3.8 mg of sodium borohydride was weighed and dissolved into 10 mL of deionized water to obtain a sodium borohydride reducing solution with a concentration of 1×10−2 mol/L. Under magnetic stirring, 1 mL of sodium borohydride solution with a concentration of 1×10−2 mol/L was fast added to the palladium chloride aqueous solution. After reaction for 20 minutes, 20 mL of sol containing Pd nanoparticles was obtained with a Pd content of 5×10−5 mol/L.
Preparation of Al2O3@Pd was described below.
0.20 g of polyvinylpyrrolidone was dissolved in 4 mL of deionized water under a room temperature, 2.4 mL of 5×10−5 mol/L of sol containing Pd nanoparticles was added and stirred for 12 hours, 6 mL of 1 mol/L of Al2(SO4)3 solution and 10 mL of 10% (V/V) of PEG100 aqueous solution were added with stirring, 20 mL of 2 mol/L of urea was then slowly added dropwise. The mixed solution was stirred and reacted in a water bath at 100° C. for 2.5 hours, aged for 2 hours, filtered, washed, dried, and heat-treated at 1200° C. for 1 hour to obtain Al2O3 powder coating Pd, referred hereafter as Al2O3@Pd.
Preparation of Zn0.99Al2O4:Cr3+0.0005@Al2O3@Pd1×10−5 was described below.
0.7573 g of zinc oxalate (ZnC2O4.2H2O), 0.4078 g of Al2O3@Pd, 0.0009 g of chromium oxalate hexahydrate (Cr2(C2O4)3.6H2O) were weighed and placed in an agate mortar, sufficient ground to form well mixed powder. The powder was transferred to a corundum crucible, heated at 1400° C. for 2 hours in a muffle furnace. Next, the powder was sintered at 1400° C. for 0.5 hour, then cooled to room temperature and ground to obtain zinc aluminate luminescent material of Zn0.99Al2O4:Cr3+0.0005@Al2O3@Pd1×10−5 coating Pd nanoparticles.
This example describes a process of preparation of Zn0.98Al2O4:Eu3+0.02@Al2O3@Au1.5×10−4 by using high-temperature solid-phase method.
Preparation of sol containing Au nanoparticles was described below.
2.1 mg of chloroauric acid (AuCl3.HCl.4H2O) was dissolved in 16.8 mL of deionized water. After the chloroauric acid was fully dissolved, 14 mg of sodium citrate and 6 mg of cetyl trimethyl ammonium bromide were weighed and dissolved into the chloroauric acid aqueous solution under magnetic stirring. 1.9 mg of sodium borohydride and 17.6 mg of ascorbic acid were weighed and dissolved into 10 mL of deionized water, respectively, to obtain a 10 mL of sodium borohydride solution with a concentration of 1×10−2 mol/L and a 10 mL of ascorbic acid solution with a concentration of 1×10−2 mol/L. Under magnetic stirring, 0.08 mL of sodium borohydride solution was firstly added to the chloroauric acid aqueous solution, after stirring for 5 minutes, 3.12 mL of ascorbic acid solution with a concentration of 1×10−2 mol/L was then added to the chloroauric acid aqueous solution. After reaction for 30 minutes, 20 mL of sol containing Au nanoparticles was obtained with an Au content of 5×10−4 mol/L.
Preparation of Al2O3@Au was described below.
0.5 g of PVP was dissolved in 10 mL of deionized water under a room temperature, 10.8 mL of 5×10−4 mol/L of sol containing Au nanoparticles was added and stirred for 24 hours, 6 mL of 0.5 mol/L of Al2(SO4)3 solution and 5 mL of 5% (V/V) of PEG20000 aqueous solution were added with stirring, 20 mL of 3 mol/L of urea was then slowly added dropwise. The mixed solution was stirred and reacted in a water bath at 80° C. for 1.5 hours, aged for 12 hours, filtered, washed, dried, and heat-treated at 800° C. for 2 hours to obtain Al2O3 powder coating Au, referred hereafter as Al2O3@Au.
Preparation of Zn0.98Al2O4:Eu3+0.02@Al2O3@Au1.5×10−4 was described below.
0.3073 g of zinc carbonate (ZnCO3), 0.2549 g of Al2O3@Au, 0.0121 g of europium carbonate (Eu2(CO3)3) were weighed and placed in an agate mortar, sufficient ground to form well mixed powder. The powder was transferred to a corundum crucible, heated at 800° C. for 15 hours in a muffle furnace. Next, the powder was sintered at 1000° C. for 4 hours, then cooled to room temperature and ground to obtain zinc aluminate luminescent material of Zn0.98Al2O4:Eu3+0.02@Al2O3@Au1.5×10−4 coating Au nanoparticles.
This example describes a process of preparation of Zn0.99Al2O4:Tb3+0.01@Al2O3@Ag2.5×10−4 by using high-temperature solid-phase method.
Preparation of sol containing Ag nanoparticles was described below.
3.4 mg of silver nitrate (AgNO3) was dissolved in 18.4 mL of deionized water. After the silver nitrate was fully dissolved, 42 mg of sodium citrate was weighed and dissolved into the silver nitrate aqueous solution under magnetic stirring. 5.7 mg of sodium borohydride was weighed and dissolved into 10 mL of deionized water to obtain a 10 mL of sodium borohydride solution with a concentration of 1.5×10−2 mol/L. Under magnetic stirring, 1.6 mL of sodium borohydride solution (1.5×10−2 mol/L) was added to the silver nitrate aqueous solution. After reaction for 10 minutes, 20 mL of sol containing Ag nanoparticles was obtained with an Ag content of 1×10−3 mol/L.
Preparation of Al2O3@Ag was described below.
0.1 g of polyvinylpyrrolidone was dissolved in 4 mL of deionized water under a room temperature, 3 mL of 1×10−3 mol/L of sol containing Ag nanoparticles was added and stirred for 12 hours, 12 mL of 1 mol/L of Al(NO3)3 solution and 6 mL of 4% (V/V) of polyvinyl alcohol aqueous solution were added with stirring, NH3.H2O was then slowly added dropwise under vigorous stirring until pH=9. The mixed solution was stirred and reacted for 3 hours, aged for 6 hours, filtered, washed, dried, and heat-treated at 900° C. for 4 hours to obtain Al2O3 powder coating Ag, referred hereafter as Al2O3@Ag.
Preparation of Zn0.99Al2O4:Tb3+0.01@Al2O3@Ag2.5×10−4 was described below.
0.3223 g of zinc oxide (ZnO), 0.4078 g of Al2O3@Ag, 0.0074 g of terbium oxide (Tb4O7) were weighed and placed in an agate mortar, sufficient ground to form well mixed powder. The powder was transferred to a corundum crucible, heated at 1250° C. for 4 hours in a muffle furnace. Next, the powder was sintered and reduced at 1200° C. in a tube furnace under a weak reducing atmosphere of 95%N2+5%H2 for 2 hours, then cooled to room temperature and ground to obtain zinc aluminate luminescent material of Zn0.99Al2O4:Tb3+0.01@Al2O3@Ag2.5×10−4 coating Ag nanoparticles.
This example describes a process of preparation of Zn0.95Al2O4:Eu3+0.05@Al2O3@Pt5×10−3 by using high-temperature solid-phase method.
Preparation of sol containing Pt nanoparticles was described below.
103.6 mg of chloroplatinic acid (H2PtCl6.6H2O) was dissolved, in 17 mL of deionized water. After the chloroplatinic acid was fully dissolved, 40.0 mg of sodium citrate and 60.0 mg of sodium lauryl sulfate were weighed and dissolved into the chloroplatinic acid aqueous solution under magnetic stirring. 1.9 mg of sodium borohydride was weighed and dissolved into 10 mL of deionized water to obtain 10 mL of sodium borohydride aqueous solution with a concentration of 5×10−3 mol/L. 10 mL of hydrazine hydrate solution (5×10−2 mol/L) was prepared at the same time. Under magnetic stirring, 0.4 mL of sodium borohydride solution was added dropwise to the chloroplatinic acid aqueous solution and stirred for 5 minutes, then 2.6 mL of hydrazine hydrate (5×10−2 mol/L) was added dropwise to the chloroplatinic acid aqueous solution. After reaction for 40 minutes, 10 mL of sol containing Pt nanoparticles was obtained with a Pt content of 1×10−2 mol/L.
Preparation of Al2O3@Pt was described below.
0.30 g of polyvinylpyrrolidone (PVP) was dissolved in 5 mL of deionized water under a room temperature, 6 mL of 1×10−2 mol/L of sol containing Pt nanoparticles was added and stirred for 18 hours, 12 mL of 1 mol/L of AlCl3 solution and 5 mL of isopropanol were added with stirring, 30 mL of 4 mol/L of NH4HCO3 was then slowly added dropwise. The mixed solution was stirred and reacted for 5 hours, aged for 4 hours, filtered, washed, dried, and heat-treated at 500° C. for 8 hour to obtain Al2O3 powder coating Pt, referred hereafter as Al2O3@Pt.
Preparation of Zn0.95Al2O4:Eu3+0.05@Al2O3@Pt5×10−3 was described below.
0.8341 g of zinc acetate (Zn(CH3COO)2.2H2O), 0.4078 g of Al2O3@Pt, 0.0658 g of europium acetate (Eu(CH3COO)3) were weighed and placed in an agate mortar, sufficient ground to form well mixed powder. The powder was transferred to a corundum crucible, heated at 1100° C. for 10 hours in a muffle furnace. Next, the powder was sintered at 1000° C. for 6 hours, then cooled to room temperature and ground to obtain zinc aluminate luminescent material of Zn0.95Al2O4:Eu3+0.05@Al2O3@Pt5×10−3 coating Pt nanoparticles.
This example describes a process of preparation of Zn0.98Al2O4:Ce3+0.01,Tb3+0.01@Al2O3@Cu1×19−4 by using high-temperature solid-phase method.
Preparation of sol containing Cu nanoparticles was described below.
2.4 mg of copper nitrate was dissolved in 16 mL of ethanol. After the copper nitrate was fully dissolved, 12 mg of PVP was added with stirring. 0.4 mg of sodium borohydride was dissolved into 10 mL of ethanol to obtain a sodium borohydride alcoholic solution with a concentration of 1×10−3 mol/L. 4 mL of sodium borohydride alcoholic solution was added dropwise to the copper nitrate solution. After stirring and reacting for 10 minutes, 20 mL of sol containing Cu nanoparticles was obtained with a Cu content of 6×10−4 mol/L.
Preparation of Al2O3@Cu was described below.
0.18 g of PVP was dissolved in 8 mL of deionized water under a room temperature, 2 mL of 6×10−4 mol/L of sol containing Cu nanoparticles was added and stirred for 24 hours, 6 mL of 2 mol/L of AlCl3 solution and 8 mL of 5% (V/V) of PEG10000 were added with stirring, 15 mL of 3 mol/L of NH4HCO3 was then slowly added dropwise. The mixed solution was stirred and reacted in a 60° C. water bath for 5 hours, aged for 10 hours, filtered, washed, dried, and heat-treated at 600° C. for 6 hours to obtain Al2O3 powder coating Cu, referred hereafter as Al2O3@Cu.
Preparation of Zn0.98Al2O4:Ce3+0.01,Tb3+0.01@Al2O3@Cu1×10−4 was described below.
0.3191 g of zinc oxide (ZnO), 0.4078 g of Al2O3@Cu, 0.0069 g of cerium oxide (CeO2), and 0.0074 g of terbium oxide (Tb4O7) were weighed and placed in an agate mortar, sufficient ground to form well mixed powder. The powder was transferred to a corundum crucible, heated at 1100° C. for 10 hours in a muffle furnace. Next, the powder was sintered and reduced at 1000° C. in a tube furnace under a pure H2 reducing atmosphere for 6 hours, then cooled to room temperature and ground to obtain zinc aluminate luminescent material of Zn0.98Al2O4:Ce3+0.01,Tb3+0.01@Al2O3@Cu1×10−4 coating Cu nanoparticles.
This example describes a process of preparation of Zn0.9Al2O4:Eu3+0.1@Al2O3@(Ag0.5/Au0.5)1.25×10−3 by using high-temperature solid-phase method.
Preparation of sol containing Ag0.5/Au0.5 nanoparticles was described below.
6.2 mg of chloroauric acid (AuCl3.HCl.4H2O) and 2.5 mg of AgNO3 were dissolved in 28 mL of deionized water. After they were fully dissolved, 22 mg of sodium citrate and 20 mg of PVP were weighed and added to the mixture solution under magnetic stirring. 5.7 mg of sodium borohydride was dissolved into 10 mL of deionized water to obtain a sodium borohydride aqueous solution with a concentration of 1.5×10−2 mol/L. 2 mL of sodium borohydride aqueous solution (1.5×10−2 mol/L) was added to the mixture solution. After stirring and reacting for 20 minutes, 30 mL of sol containing Ag0.5/Au0.5 nanoparticles was obtained with a sum metal (Ag+Au) content of 1×10−3 mol/L.
Preparation of Al2O3@(Ag0.5/Au0.5) was described below.
0.25 g of PVP was dissolved in 6 mL of deionized water under a room temperature, 10 mL of 1×10−3 mol/L of sol containing Ag0.5/Au0.5 nanoparticles was added and stirred for 24 hours, 8 mL of 1 mol/L of AlCl3 solution and 5 mL of glycol were added with stirring, 20 mL of 5 mol/L of (NH4)2CO3 was then slowly added dropwise. The mixed solution was stirred and reacted in a 70° C. water bath for 3 hours, aged for 4 hours, filtered, washed, dried, and heat-treated at 900° C. for 3 hours to obtain Al2O3 powder coating Ag and Au, referred hereafter as Al2O3@(Ag0.5/Au0.5).
Preparation of Zn0.9Al2O4:Eu3+0.1@Al2O3@(Ag0.5/Au0.5)1.25×10−3 was described below.
1.0709 g of zinc nitrate (Zn(NO3)2.6H2O), 0.4078 g of Al2O3@(Ag0.5/Au0.5), 0.1784 g of europium nitrate (Eu(NO3)3.6H2O) were weighed and placed in an agate mortar, sufficient ground to form well mixed powder. The powder was transferred to a corundum crucible, heated at 1000° C. for 15 hours in a muffle furnace. Next, the powder was sintered at 1000° C. for 4 hours, then cooled to room temperature and ground to obtain zinc aluminate luminescent material of Zn0.9Al2O4:Eu3+0.1@Al2O3@(Ag0.5/Au0.5)1.25×10−3 coating Ag and Au nanoparticles.
Although the present invention has been described with reference to the embodiments thereof and the best modes for carrying out the present invention, it is apparent to those skilled in the art that a variety of modifications and changes may be made without departing from the scope of the present invention, which is intended to be defined by the appended claims.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CN2012/081253 | 9/11/2012 | WO | 00 | 3/11/2015 |
