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    • 专利摘要:
    The invention relates to a method for manufacturing nanoparticles of a photoluminescent material, comprising the following successive steps: a) forming nanometric particles of said photoluminescent material; b) providing a dispersion containing the particles in a non-aqueous solvent, the dispersion further containing at least one silane coupling agent; c) placing the dispersion in an autoclave at a pressure of between 2 MPa and 100 MPa; and d) recovering the particles.
    公开号:FR3053353A1
    申请号:FR1656171
    申请日:2016-06-30
    公开日:2018-01-05
    发明作者:Abdelhay Aboulaich；Genevieve Chadeyron；Rachid Mahiou
    申请人:Centre National de la Recherche Scientifique CNRS；Universite Blaise Pascal Clermont Ferrand II；Aledia；Sigma Clermont；
    IPC主号:
    专利说明:

    Field
    The present application relates to the methods of manufacturing particles of a photoluminescent material.
    Presentation of the prior art
    A photoluminescent material, also called a phosphor, is adapted, when excited by light at a first wavelength, to emit light at a second wavelength different from the first wavelength. Photoluminescent materials are used in particular for the preparation of fluorescent coatings, in particular for the manufacture of display screens, projectors, in particular plasma screens, lamps for the backlighting of liquid crystal screens, light emitting diodes, plasma excitation lamps, trichromatic lamps, etc.
    An example of a photoluminescent material is the yttrium and aluminum garnet activated by the trivalent cerium ion (Y3AI5O12: Ce ^ +), also called YAG (English acronym for Yttrium Aluminum Garnet) YAG: Ce or YAG: Ce ^ + . This photoluminescent material
    0 is used in particular to generate white light after association with a blue light-emitting diode (LED). To do this, the blue LED is covered with a coating containing
    B15141 - Sub-micron phosphors of YAG particles: Ce ^ + . Part of the blue light is converted into yellow light by the photoluminescent coating, which makes it possible to obtain white light.
    Photoluminescent materials can be made by solid state reactions. For example, in the case of YAG: Ce, solid precursors of aluminum, yttrium and cerium, in the form of powders, are mixed, ground and heated at high temperatures, for example at temperatures above 1600 ° C. , to form a powder of particles having the desired composition and crystalline phase. An annealing of the powder is then carried out under a reducing atmosphere, generally under hydrogen (¾), to reduce the Ce ^ + ions, which have no photoluminescence property and which act as traps for the charge carriers, in ions Ce ^ + which have the desired photoluminescence properties. The photoluminescent particles obtained have a good quality crystal structure. They can then be dispersed in a matrix, for example resin, to form a photoluminescent coating.
    The methods of manufacturing particles of a photoluminescent material comprising reactions in the solid state make it possible to manufacture particles whose average size is greater than a micrometer, for example varying from 10 μm to 15 μm. For certain applications, it is desirable to manufacture particles whose average size is less than 1 μm, such particles being indifferently called nanoparticles, nanometric particles or submicron particles thereafter. This is the case in particular when it is desired to produce a fluid or viscous composition comprising the photoluminescent particles so as to be able to implement a process for applying the photoluminescent particles called additive, for example by direct printing of the composition comprising the particles photoluminescent at the desired locations. However, the production of a fluid composition comprising
    B15141 - Sub-micron phosphors photoluminescent particles which is stable over time requires the use of nanoparticles.
    To manufacture nanoparticles, it is known to implement a so-called topdown or topdown synthesis method which consists in grinding particles of the photoluminescent material of average size greater than a micrometer obtained by reactions in the solid state, for example in a grinder. to reduce the average particle size. However, the grinding operation results in the formation of defects on the surface of the particles obtained, from which there results a reduction in the photoluminescence performance of the photoluminescent nanoparticles, in particular the external quantum yield of the particles. In addition, agglomeration phenomena of nanometric particles obtained by grinding can be observed, which leads to the formation of clusters of large particles.
    It is known to produce particles of a photoluminescent material by so-called bottom-up or bottom-up methods which make it possible to obtain submicron particles. Bottom-up synthesis methods are chemical synthesis methods which rely on the assembly of small chemical entities (atoms or molecules) to make larger objects, nanoparticles in this case. Among the bottom-up methods, there may be mentioned, for example, the sol-gel process and the solvothermal or hydrothermal process. The common point of bottom-up methods is that syntheses of nanoparticles are generally carried out at lower temperatures compared to those of reactions in the solid state. Due to these low synthesis temperatures, photoluminescent nanoparticles generally suffer from a low degree of crystallinity giving rise to structural defects which are often associated with charge carrier or luminescence traps. Thus, the performance in terms of light output of the photoluminescent nanoparticles obtained by these methods is significantly lower than that of
    B15141 - Sub-micron phosphors photoluminescent particles of average size greater than a micrometer produced by reactions in solid phase.
    It would be desirable to obtain a powder of nanoparticles of a photoluminescent material whose performance, in particular in terms of light output, is greater than that obtained for nanoparticles of the same photoluminescent material obtained by bottom-up methods. summary
    An object of an embodiment aims to overcome all or part of the drawbacks relating to the methods of manufacturing photoluminescent particles described above.
    Another object of an embodiment is that the average particle size is less than 1 µm.
    Another object of an embodiment is that 100% of the particles (d] _oo) are less than 1 µm in size.
    Another object of an embodiment consists in remedying the surface defects of the nanoparticles obtained after a grinding step.
    Another object of an embodiment is that the external quantum yield of the nanometric particles is greater than 60% and that the internal quantum yield is at least equal to 70%.
    Another object of an embodiment is to allow the production of colloidal dispersions stable over time.
    Another object of an embodiment is that the surface of the synthesized nanoparticles is compatible with the solvent (s) and / or the encapsulants used for the implementation of a phosphor.
    Another object of an embodiment is that the dispersions of photoluminescent nanoparticles are compatible with the method of depositing the phosphor on the light-emitting diodes.
    Thus, one embodiment provides a method for manufacturing nanoparticles from a photoluminescent material, comprising the following successive steps:
    B15141 - Sub-micron phosphors
    a) forming nanometric particles of said photoluminescent material;
    b) producing a dispersion containing the particles in a non-aqueous solvent, the dispersion containing, in addition, at least one coupling agent of silane type;
    c) place the dispersion in an autoclave at a pressure between 2 MPa and 100 MPa; and
    d) recover the particles.
    According to one embodiment, step b) is preceded by a surface treatment of the nanometric particles with a silica precursor.
    According to one embodiment, the silane coupling agent is an organo-functional compound having the following chemical formula:
    R n SiX4_ n where n is equal to 1, 2 or 3, X denotes a hydrolysable group, and R is a non-hydrolysable organic group.
    According to one embodiment, X is an alkoxy group, a halide group or an amine group.
    According to one embodiment, the non-aqueous solvent is an alcohol.
    According to one embodiment, step a) comprises the grinding of particles of said photoluminescent material whose average size is greater than 1 μm to obtain the nanometric particles.
    According to one embodiment, the particles of said photoluminescent material whose average size is greater than 1 μm are ground in a humid environment.
    According to one embodiment, the particles of said photoluminescent material whose average size is greater than 1 μm are ground in a solvent different from the nonaqueous solvent used in step b).
    According to one embodiment, the duration of step c) is between 30 minutes and 48 hours.
    B15141 - Sub-micron phosphors
    According to one embodiment, the temperature in the autoclave is between 25 ° C and 300 ° C.
    According to one embodiment, the photoluminescent material is an aluminate, a silicate, a nitride, a fluoride or a sulfide.
    According to one embodiment, the photoluminescent material mainly comprises a yttrium and aluminum oxide or a lutetium and aluminum oxide containing, in addition, at least one of the following elements: cerium, europium, chromium, neodymium, terbium , dysprosium, praseodymium or gadolinium.
    According to one embodiment, the method further comprises, before step c), a step of mixing and treating in the autoclave the nanometric particles in the presence of all or part of the precursors used to form the nanometric particles .
    According to one embodiment, the method further comprises, before step c), a step of mixing the nanometric particles with at least one photoluminescent substance.
    According to one embodiment, the photoluminescent substance is a quantum dot.
    According to one embodiment, the nanometric particles are quantum dots.
    Brief description of the drawings
    These characteristics and advantages, as well as others, will be explained in detail in the following description of particular embodiments made without implied limitation in relation to the attached figures, among which:
    FIG. 1 represents, in the form of a block diagram, an embodiment of a method for manufacturing nanometric particles of a photoluminescent material;
    Figure 2 is a sectional, partial and schematic view of an autoclave;
    Figure 3 is a partial and schematic sectional view of an embodiment of nanoparticles of a
    B15141 - Sub-micron phosphors photoluminescent material obtained by the process illustrated in Figure 1;
    Figure 4 is a sectional view, partial and schematic, of a detail of part of a nanoparticle shown in Figure 3;
    Figures 5 to 7 are sectional views, partial and schematic, of a particle of photoluminescent material obtained by variants of the method illustrated in Figure 1;
    FIG. 8 represents, in the form of a block diagram, another embodiment of a method for manufacturing nanoparticles of a photoluminescent material;
    FIG. 9 schematically represents a nanoparticle at the stages of the process illustrated in FIG. 8;
    Figures 10 to 12 are grain size curves of powders of photoluminescent particles;
    FIG. 13 represents curves of evolution of the intensity of photoluminescence as a function of the wavelength of the radiation emitted by photoluminescent materials;
    FIG. 14 is a said X-ray fractogram representative of an example of photoluminescent nanoparticles;
    Figures 15 to 18 are grain size curves of powders of photoluminescent particles; and FIG. 19 represents curves of evolution of the intensity of photoluminescence as a function of the wavelength of the radiation emitted by photoluminescent materials. detailed description
    For the sake of clarity, the same elements have been designated by the same references in the different figures. In addition, in the following description, the expressions substantially, approximately and approximately mean to within 10%.
    By particles of a material is meant unitary elements of the material. The term particle as used in the context of the present application must be understood in a broad sense and corresponds not only to compact particles having more or less a spherical shape but also to particles
    B15141 - Sub-micron angular phosphors, flattened particles, flake-like particles, fiber-like particles, or fibrous particles, etc. It will be understood that the particle size in the context of the present invention means the smallest transverse dimension of the particles. For example, in the case of particles in the form of fibers, the size of the particles corresponds to the diameter of the fibers.
    By the term average size is meant according to the present invention the size of the particle which is greater than the size of 50% by volume of the particles and less than the size of 50% by volume of the particles of a distribution of particles. This corresponds to dgo- Thus, an average size which is less than the size of 100% by volume particles of a distribution corresponds to d] _oo · θ η micron particle means a particle whose average size is between 1 pm and 100 pm, typically between 1 pm and 50 pm. Nanoparticles are understood to mean particles whose average size is less than 1 μm, preferably between 5 nm and 500 nm. The particle size of the micron particles can be measured by laser particle size using, for example, a Malvern Mastersizer 2000. The particle size of the submicron particles or nanoparticles can be measured by Dynamic Light Diffusion (DDL) using, for example, a Zetasizer Nano ZS de Malvern.
    One embodiment of the process for manufacturing nanoparticles of a photoluminescent material comprises carrying out a dispersion of nanoparticles in a non-aqueous solvent with at least one coupling agent of silane type and maintaining the dispersion in an autoclave at a temperature between 50 ° C and 300 ° C and a pressure between 2 MPa and 100 MPa, preferably between 2 MPa and 10 MPa, from 30 minutes to 48 hours. The nanometric particles can be obtained by grinding particles of average size greater than 1 μm obtained by manufacturing processes in the solid state. AT
    B15141 - Sub-micron phosphors alternatively, nanoparticles can be formed directly by bottom-up methods.
    FIG. 1 represents, in the form of a block diagram, an embodiment of a method for manufacturing nanoparticles of a photoluminescent material. The method comprises successive steps 10 to 16.
    In step 10, particles of average size greater than 1 μm are produced by a known method of manufacturing particles of a photoluminescent material. By way of example, the method comprises reactions in the solid state. By way of example, solid precursors of the components of the photoluminescent material in the form of powders are mixed, ground and heated at high temperatures, for example at temperatures above 1600 ° C., to form a powder of particles having the composition and the crystalline phase desired. Annealing of the powder can be carried out under a reducing atmosphere, for example under hydrogen (Hg).
    According to one embodiment, the photoluminescent material is an aluminate, a silicate, a nitride, a fluoride or a sulfide. As an example, the photoluminescent material is adapted to emit light at a wavelength in the range from 400 nm to 700 nm under light excitation at a wavelength in the range from 250 nm to 500 nm, preferably from 400 nm to 480 nm.
    According to one embodiment, the photoluminescent material mainly comprises an aluminate, in particular an aluminum and yttrium garnet according to the following formula (1):
    ( y (1-x) r1 x) 3 ( A1 (ly) R2 y) 5 ° 12 (D where a garnet of aluminum and lutetium according to the following formula (2):
    (LU (ix) r1 x) 3 (Al (1_y) R 2 y) 5 O 12 (2) where R 2 and R 2 are independently chosen from elements comprising rare earths, alkaline earths and transition metals and x and y each vary independently from 0 to 1. Preferably, R 2 and R 2 are independently chosen from
    B15141 - Sub-micron phosphors group including cerium, samarium, gadolinium, silicon, barium, terbium, strontium, chromium, praseodymium and gallium.
    As an example of nitrides absorbing and emitting light in the desired wavelength ranges, there may be mentioned: CaAlSiN 3 : Eu, (Ca, Sr) AlSiN 3 : Eu, Ca 2 Si 5 N 8 : Eu or (Ca, Sr) If 5 N 8 : Eu.
    By way of example of fluorides absorbing and emitting light in the desired wavelength ranges, mention may be made of fluorides of formula X 2 MF 8 : Mn (where X can be K or Na and M can be Si, Ge, Sn or Ti).
    By way of example of sulfides absorbing and emitting light in the desired wavelength ranges, there may be mentioned: CaS: Eu, SrCa: Eu, (Sr, Ca) S: Eu and SrGa 2 S 4 : Eu .
    By way of example of an aluminate absorbing and emitting light in the desired wavelength ranges, there may be mentioned: Y 3 Al 5 O 12 : Ce, (Y, Gd) 3 A1 5 O 12 : Ce, Tb 3 Al 5 O 12 , (Y, Tb) 3 A1 5 O 12 , Lu 3 A1 5 O 12 : Ce and Y 3 (Al, Ga) 5 O 12 .
    By way of example of silicates absorbing and emitting light in the desired wavelength ranges, there may be mentioned: (Sr, Ba) 2 SiO 4 : Eu, Sr 2 SiO 4 : Eu, Ba 2 SiO 4 : Eu, Ca 2 SiO 4 : Eu, Ca 3 SiO5: Eu and Sr 3 SiO5: Eu.
    At the end of step 10, the average size of the photoluminescent particles is greater than 1 μm and can be between 10 μm and 15 μm.
    In step 12, the average size of the photoluminescent particles obtained in step 10 is reduced by grinding the particles, for example using a ball or ball mill. The grinding is preferably a wet grinding in which the particles are dispersed in a solvent. The solvent is preferably a nonaqueous solvent, in particular a polar and protic nonaqueous solvent. According to one embodiment, the solvent is an alcohol, preferably chosen from the group comprising methanol, ethanol, propanol, butanol, pentanol, hexanol and isopropanol, in particular ethanol. AT
    B15141 - Sub-micron phosphors at the end of step 12, the average size of the photoluminescent particles is less than 1 μm, for example between 100 nm and 500 nm.
    In step 14, a functionalization of the nanometric particles is carried out. For this purpose, a colloidal dispersion of the photoluminescent particles ground in a non-aqueous solvent, that is to say comprising less than 0.02% by weight of water, is formed. The nonaqueous solvent is preferably a polar and protic nonaqueous solvent. According to one embodiment, the non-aqueous solvent is an alcohol, in particular chosen from the group comprising methanol, ethanol, propanol, butanol, pentanol, hexanol and isopropanol. According to one embodiment, the colloidal dispersion comprises from 10 mg to 100 mg of photoluminescent particles per ml of solvent (10 mg / ml 100 mg / ml). The solvent can be the same as that used in step 12. When the solvent used in step 14 is the same as that used in step 12, the colloidal dispersion of photoluminescent nanoparticles can correspond to the dispersion obtained at end of step 12. However, it may be advantageous to use in step 14 a solvent which is different from the solvent used in step 12. Indeed, it may be desirable to use a first solvent at the end of step 12. step 12 which improves the performance of the grinding operation, for example a solvent having a low viscosity, and a second solvent more suitable for the treatment carried out in step 14, for example a solvent having a higher boiling temperature than the solvent used in step 12.
    To carry out the surface treatment in step 14, the colloidal dispersion is placed in an autoclave.
    FIG. 2 represents an embodiment of an autoclave 20 which can be used in step 14. The autoclave 20 comprises an enclosure 21 in which the product 22 to be treated is placed. A line 23 allows the supply of gas into the enclosure
    21. The opening and closing of the pipe 23 is controlled by a valve 24. A pipe 25 allows the sampling
    B15141 - Sub-micron sample phosphors in the enclosure 21. The opening and closing of the pipe 25 is controlled by a valve 26. The enclosure 21 is partially surrounded by a heating collar 27. A pressure sensor 28 allows the measurement of the pressure in the enclosure
    21. An agitator 29 driven by a motor 30 makes it possible to agitate the product 22 in the enclosure 21. A control module 31, comprising for example a computer, is connected to the pressure sensor 28, to the heating collar 27, to the valves 24, 26 and to the motor 30. The control module 31 is suitable for controlling the heating collar 27 and the valves 24, 26. The control module 31 makes it possible to regulate the temperature and the pressure in the enclosure 21 and can control the starting and stopping the agitator 29.
    Considering again FIG. 1, according to one embodiment, the pressure in the autoclave is kept substantially constant throughout the duration of step 14. For example, the pressure in the autoclave can vary between 20 bars (2 MPa) and 100 bars (10 MPa) depending on the solvent used and the heating temperature. The pressure can also be adjusted by introducing a gas, for example nitrogen, into the autoclave. According to one embodiment, the temperature in the autoclave is kept substantially constant throughout the duration of step 14. For example, the temperature in the autoclave is between 25 ° C and 300 ° C, from preferably between 150 ° C and 250 ° C. Agitation of the particles in the dispersion can be carried out in the autoclave.
    According to one embodiment, at least one coupling agent of the silane type is added to the colloidal dispersion of photoluminescent particles before its placement in the autoclave. The expression “silane coupling agent, silane coupling agent or silane coupling agent” is understood to mean, according to the present description, a reagent capable of binding by chemical bonds or physical bonds with a matrix or a solvent in which the particles are dispersed and able to chemically bond with the surface of the particles. Each silane coupling agent comprises a first part
    B15141 - Sub-micron phosphors capable of binding with the matrix or the solvent and a second part capable of binding with the surface of the particles. According to one embodiment, the colloidal dispersion comprises from 1 mg to 100 mg of coupling agents per ml of solvent. The mass ratio between the silane coupling agent and the luminescent nanoparticles can vary between 1 and 0.01.
    Silane coupling agents tend to be distributed around the periphery of each photoluminescent particle and to form a more or less dense layer surrounding each particle.
    Figure 3 is a partial and schematic sectional view of an embodiment of the colloidal dispersion obtained at the end of step 14. Each particle 32 of the photoluminescent material is surrounded by a layer 31 of coupling. The covering of each particle 32 by the coupling agents can be more or less complete. All the parts of the coupling agents which are not capable of binding with the particle are oriented towards the outside of the particle, which is illustrated by the appendices 34 in FIG. 3.
    A silane coupling agent is an organofunctional compound having the following chemical formula (3):
    R n SiX 4 _ n (3) where n is equal to 1, 2 or 3, X denotes a hydrolysable group, in particular an alkoxy group, a halide group or an amine group, and R is a non-hydrolysable organic group. By way of example, the organosilane has the formula R n Si (OR ') 4 _ n .
    According to one embodiment, the silane coupling agents are chosen from the group comprising for example: n-propyltrimethoxysilane, allyltrimethoxysilane, n-propyltriethoxysilane, trimethoxy (7-octen-1-yl) silane, trimethoxy (octadecyl) silane, n- octyltrimethoxysilane, n-octyltriethoxysilane, methoxy (triethyleneoxy) propyltrimethoxysilane, 3-aminopropyltrimethoxysilane, phenylrimethoxysilane, dimethoxy (methyl) octylsilane, 3-mercaptopropyltrimethoxysilylimethylpropyl),
    B15141 - Sub-micron phosphors isocyanatopropyltrimethoxysilane, 2- [methoxy (polyethyleneoxy) 69propyl] trimethoxysilane, 3-glycidoxypropyltrimethoxysilane, N (3-acryloxy-2-hydroxypropyl) -3-aminopropyltriethoxysilane and bis [3- (triethoxyl)
    According to one embodiment, the silane coupling agents can be carbon chlorosilanes such as for example: chloro (dimethyl) octadecylsilane, chloro (dodecyl) dimethylsilane or chloro (decyl) dimethylsilane or fluorinated chlorosilanes such as for example: chloro-dimethyl ( 3,3,3 trifluoropropyl) silane or perfluorodecyltrichlorosilane.
    According to one embodiment, the coupling agents can, in addition, react with each other on the surface of the particles and form a new compound which surrounds, in whole or in part, each particle.
    According to one embodiment, the organosilanes react in the non-aqueous solvent to form Si-O-Si bonds. Advantageously, the reaction of the organosilanes in a non-aqueous medium does not lead to the formation of silanols (Si— OH). It is recognized that the presence of hydroxy-type groups (-OH), such as for example Si-OH groups, on the surface of photoluminescent particles has a negative effect on the light output of the particles (in particular because these groups form traps for load carriers).
    For example, it is known that the reaction of a silicon chloride (S1CI4) with an anhydrous ether of formula RO-R can give rise to SiOg particles with surface groups of Si-OR type only according to the following equations (4), (5) and (6):
    Hydrolysis: Si-Ci + ROR Si-OR + R-Cl (4) Condensation via: Si-OR + Si-Ci Si-O-Si + R-Cl (5) or via: Si-OR + Si-OR Si -O-Si + ROR (6)
    Figure 4 is a sectional view, partial and schematic, of a particle 32 surrounded by a layer 33 of more or less dense siloxane obtained by forming bonds
    B15141 - Sub-micron phosphors
    Si-O-Si between silane coupling agents. The R groups are oriented towards the outside of the particle 32.
    Alternatively, step 14 may include a surface treatment step with all or part of the precursors used to construct the photoluminescent particle. This step can be carried out before or during the functionalization step, preferably before the surface functionalization step. For example, a surface treatment in the presence of a source of yttrium, aluminum, cerium and oxygen can be used to treat the surface of YAG: Ce nanoparticles. For CagMgSigC ^: Eu nanoparticles, all or part of the sources of silicon, magnesium, calcium, europium and oxygen can be mixed with the nanoparticles heated in the autoclave as described above. These precursors will react with each other in the dispersion and form a layer which surrounds, in whole or in part, each particle.
    FIG. 5 is a partial and schematic sectional view of a particle 32 obtained at the end of step 14 when a step of surface treatment with all or part of the precursors used to construct the photoluminescent particle has been carried out. These precursors reacted with each other in the dispersion and formed a layer 35 which surrounds, in whole or in part, the particle 32.
    According to another variant, one or more photoluminescent substances can be added to the mixture of step 14. The photoluminescent substance or substances can be of the organic, inorganic or hybrid type emitting or not emitting at the same emission wavelength as the particle 20. At the end of step 14, the photoluminescent substance will be located inside the layer formed by the coupling agents or outside this layer.
    Figure 6 is a sectional, partial and schematic view of a particle 32 obtained at the end of step 14 when photoluminescent substances are added to the mixture
    B15141 - Sub-micron phosphors in step 14. The photoluminescent substances 36 were trapped in layer 33.
    According to one embodiment, the photoluminescent substance can be a quantum dot. The quantum dot can be linked to the layer formed by the coupling agents by covalent chemical bonds. For example, 3-mercaptopropyltrimethoxysilane can be used as a coupling agent. The trimethoxysilane groups will form covalent bonds with the surface of the photoluminescent particle while the thiol group (-SH) oriented towards the outside of the particle will form a covalent bond with the surface of the quantum dot.
    FIG. 7 is a partial and schematic sectional view of a particle 32 obtained at the end of step 14 for which quantum dots 37 are linked to the surface of the layer 33.
    The duration of step 14 can be between 30 minutes and several days, preferably between 30 minutes and 48 hours, preferably between 10 hours and 20 hours. The heating time depends in particular on the heating temperature, the solvent and the coupling agents used.
    According to one embodiment, the functionalization step 14 can be preceded by an additional step for treating the surface of the nanoparticles obtained in the step
    12. This step can comprise mixing the dispersion of nanoparticles with silica precursors at room temperature for a period which varies from 1 hour to 24 hours. The precursor of silica is for example TEOS. The reaction can then be carried out in the presence of ammonia (NH4OH) according to the Stober method for example. The pretreatment step is followed by the recovery and cleaning of the nanoparticles to remove the silica precursors which have not reacted with the surface of the particles, and optionally ammonia, and the functionalization step 14 can be carried out as previously described.
    B15141 - Sub-micron phosphors
    Step 16 includes the preparation of a final product suitable for the intended application. Step 16 can comprise the recovery of the particles in the colloidal dispersion obtained at the end of step 14. The recovery step can comprise a step of precipitation of the nanoparticles, for example by adding an anti-solvent for the nanoparticles. By anti-solvent is meant any solvent which does not have a chemical affinity with the nanoparticles. The choice of this anti-solvent will depend on the nature and the surface chemistry of the nanoparticles. These anti-solvents are generally polar aprotic solvents such as acetone or polar protic solvents such as ethanol. Alternatively, the solid phase containing the nanoparticles can be recovered by centrifugation. Step 16 can be followed by a purification step for the particles, in particular for removing unreacted precursors and the parasitic reaction products as well as the solvent or solvents used in step 14. The nanoparticles are then dried, for example at a temperature between 25 ° C and 80 ° C, for a time between 1 h and 12 h. A nanoparticle powder is then obtained.
    The nanoparticle powder obtained in step 16 can be added to a solvent, optionally also containing a binder, for example a resin, to form a composition of photoluminescent particles which is fluid or viscous. The coupling agents linked to the photoluminescent particles can be chosen to improve the compatibility between the photoluminescent particles and the solvent and / or the binder, for example to increase the dispersion of the photoluminescent particles in the solvent and / or the binder.
    The process for applying the photoluminescent composition, in particular for forming a coating, can correspond to a so-called additive process, for example by direct printing of the photoluminescent composition at the desired locations, for example by inkjet printing, photogravure,
    B15141 - Sub-micron phosphors screen printing, flexography, spray coating (in English spray coating), drop deposition (in English drop-casting) or by dipping the substrate in the solution of photoluminescent nanoparticles (in English dip-coating).
    FIG. 8 represents, in the form of a block diagram, another embodiment of a method for manufacturing nanoparticles of a photoluminescent material.
    The method comprises a step 40 of manufacturing nanoparticles of the photoluminescent material which directly results in the obtaining of nanometric particles substantially without the formation of particles whose average size is greater than a micrometer. By way of example, the process for manufacturing nanoparticles is a hydrothermal process. According to one embodiment, the nanoparticles are quantum dots of the photoluminescent material.
    The quantum dots are nanocrystals of pure semiconductors (Si, Ge) or of type II-VI compounds (CdS, CdSe, CdTe, ZnO, ZnSe, ZnS), III-V (GaAs, InP, InAs, GaN), IV -VI (PbS, PbSe, PbTe), I-VII (CuCl), V-VI (Bi 2 Te 3 ) or II-V (Cd 3 As, Zn 3 P 2 , Zn 3 As 2 ), whose diameter is generally between 2 nm and 10 nm. As a direct consequence of the phenomenon of “quantum confinement”, these materials then exhibit adjustable fluorescence properties by controlling their size. Two major methods of colloidal synthesis of quantum dots have been developed over the past fifteen years: so-called organometallic and hydrothermal syntheses. Organometallic synthesis is based on the rapid injection of a precursor A at high temperature (270 ° C-300 ° C) to a precursor B (for example, in the case of CdSe, A corresponds to Se 2 _ and B corresponds to Cd 2+ ) in coordinating solvents, such as trioctylphosphine oxide (TOPO), hexadecylamine (HDA), oleylamine, or non-coordinating solvents such as 1-octadecene (ODE). Hydrothermal synthesis takes place in an aqueous medium and the injection of the precursor is generally carried out at room temperature. The mixture is then heated to reflux (100 ° C) or to
    B15141 - Sub-micron phosphors temperatures above 150 ° C in an autoclave. The most commonly used synthesis for the manufacture of quantum dots, and which achieves the highest light yields, is the organometallic type method. However, this method generates hydrophobic particles which are only miscible with organic solvents of apolar type (toluene, chloroform, hexane, etc.). Unfortunately, most of these solvents are toxic to humans and the environment. In order to make the particles miscible with other polar-type solvents (slightly or not toxic), a ligand exchange is necessary. It should be noted that the exchange of surface ligand is very often accompanied by a reduction in the quantum yield of photoluminescence of the quantum dots. Likewise, the hydrophobic ligands resulting from the synthesis of quantum dots (by organometallic route) are not compatible with all types of encapsulants used for shaping the particles, for example, silicone resins. When the hydrophobic quantum dots are mixed with a silicone resin, a strong aggregation and flocculation of particles is observed. Furthermore, quantum dots generally suffer from poor stability over time due to the oxidation of surface metals, which leads to a significant drop in light output over time. It is therefore desirable to develop a versatile surface treatment method for quantum dots which both protects the quantum dots against oxidation and provides them with specific surface functions which make them miscible with encapsulant (and in addition the non-polar solvent, if necessary) according to the desired application and shaping without this leading to a loss of light yield of the starting particles (before surface treatment).
    The method continues with steps 14 and 16 described previously in relation to the method illustrated in FIG. 1.
    In the case where the nanoparticle is a quantum dot, other specific coupling agents, other than the
    B15141 - Sub-micron organosilane phosphors, can be used. These specific coupling agents can have at least two functions of thiol type (-SH). The following coupling agents can be used: 1,6-hexanedithiol (which has two thiol functions), trimethylolpropane tris (3-mercaptopropionate) (which has three thiol functions) and pentaerythritol tetrakis (3 mercaptopropionate) (which has four thiol functions). At least one of the thiol functions reacts on the surface of nanoparticles while the remaining thiol functions are oriented towards the outside of the particle and can react with specific monomers in order to form an organic layer around the quantum dot. The specific monomers must have at least two acrylic functions (CH2 = CHCOO-) and can be for example: poly (ethylene glycol) diacrylate (which has two acrylic functions), pentaerythritol triacrylate (which has three acrylic functions), pentaerythritol tetraacrylate (which has four acrylic functions). The coupling between the thiol functions and the acrylic functions is carried out by addition reaction and gives rise to a chain of organic ligand surrounding the nanoparticle and terminated by acrylate functions. The addition reaction can be catalyzed by amines or by a radical initiator.
    FIG. 9 illustrates this embodiment in the case where pentaerythritol tetrakis (3-mercaptopropionate) is used as specific ligand and pentaerythritol tetraacrylate is used as specific monomer. The acrylate functions generated on the surface of nanoparticles can then serve as a crosslinking base to encapsulate the quantum dots in a polymer, for example PMMA, or a resin.
    Examples have been made by the inventors. For the examples comprising a grinding step, such as step 12 described above in relation to FIG. 1, this grinding step was carried out using a suspension of photoluminescent particles. This suspension was produced by mixing 10 g of photoluminescent particles in 45 mL of ethanol and 240
    B15141 - Sub-micron phosphors g of ZrOq beads 0.5 mm in diameter. The suspended particles were ground for 30 minutes and the speed of rotation of the mill was 1800 rpm.
    For the examples comprising a functionalization step for the nanoparticles, such as step 14 described previously in relation to FIG. 1, the functionalized nanoparticles were precipitated by adding excess acetonitrile. The solid phase was recovered by centrifugation, then was dried between 25 ° C and 80 ° C for 12 hours to form a powder of nanoparticles.
    Measurements of the internal quantum yield QYj_ n t, of the absorption coefficient Abs and of the external quantum yield QY e xt were performed on the photoluminescent powders and the dispersions of manufactured photoluminescent particles. The internal quantum efficiency QYj_ n t, Abs absorption coefficient and the external quantum yield QY e xt his t defined by relations (4):
    QY i nt = ^ em / ^ abs (Y
    Abs = N a p s / N exc
    QYext = QYint * Ab s where N em and N a p s are, respectively, the number of photons emitted and absorbed by the photoluminescent material, N exc is the total number of photons emitted by the excitation source. The values QYj_ n t and Abs are directly given by the measuring device. The external quantum yield QY e xt are therefore deduced from these values.
    The measurements of the internal quantum yield QYj_ n t and of the absorption coefficient Abs were carried out using a Hamamatsu CG-2 spectrophotometer (250-900 nm) equipped with an integration sphere. The external quantum yield values QY e xt are given with a margin of error of 5%.
    In Examples 1 to 6 photoluminescent particles of YAG: Ce ^ + were produced. Such particles are adapted to emit yellow light when they are excited by blue light.
    Comparison example 1
    B15141 - Sub-micron phosphors
    The powder of microparticles from YAG: Ce ^ + sold by the company FREE RADICAL TECHNOLOGY CO., LTD (Taiwan) under the reference PF-Y46W200 was used as comparison powder.
    These microparticles are obtained by synthesis by reaction in the solid state. In Example 1, a grinding step and a functionalization step were not carried out with a coupling agent.
    FIG. 10 represents the particle size curve of the powder of microparticles of YAG: Ce ^ + . The d5Q was 14 pm, the dgo was 20 pm and the d] _o was 8 pm. The maximum of the emission band is located at 558nm.
    The internal quantum efficiency QY-j_ n p, the absorption coefficient Abs and the external quantum efficiency QY e xt have been measured. The results obtained are collated in table (I) below.
    QYint Abs QYext
    0, 91 87
    Table I
    Comparison example 2
    The powder of microparticles of YAG: This ^ + of Example 1 was used to produce a powder of nanoparticles.
    A grinding stage has been carried out. No functionalization step was carried out by a coupling agent.
    FIG. 11 represents the particle size curve of the powder of YAG nanoparticles: Ce ^ + obtained after grinding.
    The internal quantum efficiency QY-j_ n p, the absorption coefficient Abs and the external quantum efficiency QY e xt have been measured. The results obtained are collated in table (II) below.
    QYint Abs QYext
    0.8 54
    Table II
    The external quantum yield QY e xt ée the powder of nanoparticles obtained by grinding the powder of Example 1
    B15141 - Sub-micron phosphors without functionalization step is more than 33 points lower than the quantum yield of the powder of Example 1.
    Comparison example 3
    A powder of YAG nanoparticles: Ce 2+ was manufactured by a solvothermal process.
    A colloidal dispersion of nanoparticles was produced by mixing 56.16 mmol of hydrated yttrium acetate, 0.05 mmol of hydrated cerium (III) acetate and 94.55 mmol of aluminum isopropoxide in a mixture of solvents comprising 450 mL of 1,4-butanediol and 60 mL of diethylene glycol. The mixture was heated in an autoclave at 300 ° C for 1 hour. The colloidal dispersion obtained was cooled to room temperature. The nanoparticles were precipitated by adding excess acetonitrile. The solid phase was recovered by centrifugation, then was dried at 80 ° C for 12 hours to form a powder of nanoparticles. The nanoparticle powder was annealed for 4 hours at 1500 ° C. Before annealing, the average size of the nanoparticles was 40 nm. After annealing, the average size of the nanoparticles was between 100 nm and 900 nm.
    The internal quantum yield QY-j_ n - (-, the absorption coefficient A * bs and the external quantum yield QY e xt have been measured. The results obtained are collated in table (III) below.
    QYint (%) QYext
    0.71 35
    Table III
    Example 4
    The powder of microparticles of YAG: Ce 2+ of Example 1
    was used to make a nanoparticle powder. A step of grinding has been carried out. A step of functionalization at summer carried out. For The stage of functionalization, the solvent was Ethanol and the agent of
    coupling was trimethoxyoctadecylsilane (TMODS, Sigma Aldrich). The nanoparticle concentration has been adjusted to
    B15141 - Sub-micron phosphors mg / mL ethanol. The mass ratio between the nanoparticles and the coupling agent was 1: 1. The dispersion was placed in an autoclave for 17 hours at 150 ° C. and at a pressure between 20 bars and 30 bars.
    The nanoparticle powder was recovered after the functionalization step by adding an excess of ethanol (anti-solvent). The addition of ethanol causes the particles to settle very quickly. This is proof that the particle surface has become hydrophobic after treatment in the autoclave in the presence of TMODS. A dispersion of the powder of functionalized nanoparticles was carried out in 1,2dichlorobenzene which is a non-polar solvent.
    FIG. 12 represents the grain size curve of the dispersion of YAG: Ce3 + nanoparticles in 1,2dichlorobenzene. The functionalized nanoparticles are substantially stable in the solvent after several weeks at room temperature.
    The internal quantum efficiency QY-j_ n p, the absorption coefficient Abs and the external quantum efficiency QY e xt have been measured. The results obtained are collated in table (IV) below.
    QYint Q ^ ext
    0.9 70 Table IV
    The external quantum yield QY e xt of the nanoparticles powder obtained in Example 4 is increased compared to the external quantum yield QY e xt of the nanoparticles powder obtained in Examples 2 and 3.
    FIG. 13 represents curves of evolution C1, C2 and C3 of the intensity of photoluminescence PL, in arbitrary unit, as a function of the wavelength λ, in nanometer, of the radiation PL emitted by the photoluminescent powders produced respectively at examples 1, 2 and 4 receiving a light radiation whose wavelength was 460 nm. The functionalization stage makes it possible to increase the intensity of
    B15141 - Sub-micron phosphors photoluminescence of the nanoparticle powder obtained after the grinding step.
    FIG. 14 shows the result of analysis by X-ray diffraction carried out on the powder of photoluminescent nanoparticles dried in air for 12 h. The result shows that all the diffraction peaks observed correspond to the crystallized phase of Y3AI5O12 · No impurity or parasitic phase is observed. The widening of the diffraction peaks confirms that the diameter of the crystallites is nanometric as has also been measured by dynamic light scattering and by transmission electron microscopy.
    Example 5
    The powder of microparticles of YAG: This ^ + of Example 1 was used to produce a powder of nanoparticles.
    A grinding stage has been carried out. A functionalization stage has been carried out. For the functionalization step, the solvent was ethanol and the coupling agent was (3-glycidoxypropyl) trimethoxysilane (GPTMS, Sigma Aldrich). The concentration of nanoparticles was adjusted to 50 mg / ml of ethanol. The mass ratio between the nanoparticles and the coupling agent was 1: 1. The dispersion was autoclaved for 25 hours at 150 ° C and at a pressure between 20 bar and 30 bar.
    The nanoparticle powder was recovered after the functionalization step by centrifugation. A dispersion of the powder of functionalized nanoparticles was carried out in diethylene glycol diethyl ether which is a polar solvent.
    FIG. 15 represents the particle size curve of the powder of YAG nanoparticles: Ce ^ + obtained after the functionalization step. This curve is close to the curve in Figure 11.
    The internal quantum yield QY-j_ n t, the absorption coefficient Abs and the external quantum yield QY e xt on t
    B15141 - Sub-micron phosphors measured. The results obtained are collated in table (V) below.
    QYint Q ^ ext
    0.860
    Table V
    The external quantum efficiency QY e xt of a powder of nanoparticles obtained in Example 5 is increased from the external quantum efficiency QY e xt of a powder of nanoparticles obtained in Examples 2 and 3.
    Example 6
    The powder of microparticles of YAG: This ^ + of Example 1 was used to produce a powder of nanoparticles.
    A grinding stage has been carried out. A pretreatment step was carried out in which the dispersion of nanoparticles obtained in the grinding step was mixed with TEOS and a 30% aqueous ammonia solution (NH4OH). The mixture is then heated at 70 ° C for 7 hours. The concentration of photoluminescent nanoparticles was adjusted to 18 mg / mL. The volume ratio between the ammonia solution and the TEOS was 0.5 ml of TEOS / 0.4 ml of NH4OH. The mass of SiOq after complete hydrolysis / condensation of TEOS represents approximately 5% of the mass of photoluminescent nanoparticles. A functionalization step was then carried out. For the functionalization step, the solvent was ethanol and the coupling agent was (3-trimethoxysilyl) propyl methacrylate (TMSPMA, Sigma Aldrich). The concentration of photoluminescent nanoparticles was adjusted to 30 mg / ml of ethanol. The mass ratio between the nanoparticles and the coupling agent was 1: 0.5. The dispersion was autoclaved for 17 hours at 150 ° C and at a pressure between 20 bar and 30 bar.
    The nanoparticle powder was recovered after the functionalization step. A dispersion of the powder of functionalized nanoparticles was carried out in tetrahydrofuran (THF) which is a polar solvent. The dispersion
    B15141 - Sub-micron phosphors of the photoluminescent nanoparticles remains stable (no settling) over time.
    FIG. 16 represents the grain size curve of the powder of YAG nanoparticles: Ce ^ + obtained after the functionalization step. This curve is close to the curve in Figure 11.
    The internal quantum efficiency QY-j_ n - | -, the absorption coefficient Abs and the external quantum efficiency QY e xt have been measured. The results obtained are collated in table (VI) below.
    QYint Q ^ ext
    0.9 67.5 Table VI
    The external quantum yield QY e xt of the nanoparticle powder obtained in Example 6 is increased compared to the external quantum yield QY e xt of the nanoparticle powder obtained in Examples 2 and 3.
    In the following examples 7 to 10, photoluminescent particles of LU3AI5O12 : Ce ^ + (LuAG: Ce) were produced. Such particles are adapted to emit green light when they are excited by blue light.
    Comparison example 7
    LuAG: Ce ^ + microparticles powder marketed by the company FREE RADICAL TECHNOLOGY CO., LTD (Taiwan) under the reference PF-X16W200 was used as comparison powder.
    These microparticles are obtained by synthesis by reaction in the solid state. In Example 7, a grinding step and a functionalization step were not carried out with a coupling agent.
    FIG. 17 represents the grain size curve of the powder of microparticles of LuAG: Ce ^ + . The dgo was 15 pm. The maximum of the emission peak was obtained for a wavelength of 534 mm.
    The internal quantum efficiency QY-j_ n - (-, the absorption coefficient Abs and the external quantum efficiency QY e xt have been
    B15141 - Sub-micron phosphors measured. The results obtained are collated in table (VII) below.
    QYint U) Q ^ ext U)
    0, 88 84
    Table VII
    Comparison example 8
    The powder of LuAG: Ce3 + microparticles of Example 7 was used to make a nanoparticle powder.
    A grinding stage has been carried out. No functionalization step was carried out by a coupling agent.
    The internal quantum yield QY-j_ n - (-, the absorption coefficient Abs and the external quantum yield QY e xt have been measured. The results obtained are collated in table (VIII) below.
    QYint U) AQ S Q ^ ext U)
    78.1 0.702 54
    Table VIII
    The external quantum yield QY e xt of the powder of nanoparticles obtained by grinding the powder of Example 8 without a functionalization step is more than 30 points lower than the quantum yield of the powder of Example 7.
    Example 9
    The LuYAG: Ce3 + microparticle powder of Example 7 was used to make a nanoparticle powder.
    A step of grinding was realized. A step of functionalization at summer carried out. For The stage of functionalization, the solvent was ethanol and the agent of
    coupling was trimethoxyoctadecylsilane. The concentration of photoluminescent nanoparticles was adjusted to 25 mg / ml of ethanol. The mass ratio between the nanoparticles and the coupling agent was 1: 1. The dispersion was autoclaved for 20 hours at 150 ° C and at a pressure between 20 bar and 30 bar.
    B15141 - Sub-micron phosphors
    The nanoparticle powder was recovered after the functionalization step. A dispersion of the powder of functionalized nanoparticles was carried out in 1,2dichlorobenzene.
    FIG. 18 represents the grain size curve of the dispersion of LuAG nanoparticles: Ce 3+ in 1,2dichlorobenzene obtained after the functionalization step.
    The internal quantum efficiency QY-j_ n p, the absorption coefficient Abs and the external quantum efficiency QY e xt have been measured. The results obtained are collated in table (X) below.
    QYint Q ^ ext 76.4 0, 824 63
    Paintings
    The external quantum yield QY e xt of the nanoparticle powder obtained in Example 10 is increased compared to the external quantum yield QY e xt of the nanoparticle powder obtained in Example 8.
    FIG. 19 represents the curves C4, C5 and C6 of evolution of the intensity of photoluminescence PL, in arbitrary unit, as a function of the wavelength λ, in nanometer, corresponding to the photoluminescent particles of examples 7, 8 and 9 under excitation at 460 nm. The functionalization stage makes it possible to increase the intensity of photoluminescence of the nanoparticle powder obtained after the grinding stage.
    Example 10
    First, YAG: Ce nanoparticles were treated with TEOS / NH4OH and functionalized with the trimethoxy (7-octen-1-yl) silane coupling agent (Sigma Aldrich) according to the same procedure used in the Example 6. After washing and purification, the photoluminescent nanoparticles were redispersed in 1,2 dichlorobenzene at a concentration of 50 mg / ml. Then, 30 mL of the nanoparticle solution was mixed with 0.1 g of methylhydro-dimethylsiloxane copolymer terminated by a trimethylsilyl function (silicon hydride,
    B15141 - Sub-micron phosphors
    PS123, United Chemical Technologies) and 0.02 g of a solution containing 0.1% by mass of platinum divinyltetramethylsiloxane (SIP6830.3, Gelest Inc.). The mixture is heated to about 50 ° C for 10 min. Then, 0.5 g of polydimethylsiloxane (PDMS) terminated by a dimethylvinyl function (PS443, United Chemical Technologies) were added to the first mixture and the final solution is heated at 70 ° C for 10 min to 15 min. The final dispersion of the particles is stable at room temperature and can be used for the deposition of nanoparticles by inkjet printing. A homogeneous composite film was produced from the final solution by a spincoating method on a glass slide. The film is then heated to 90 ° C in order to remove the solvent and to crosslink the silicone resin. The mass percentage of photoluminescent nanoparticles relative to the silicone resin in this example is approximately 70%.
    Example 11
    The dispersion of photoluminescent nanoparticles prepared in Example 6 was used. The concentration of photoluminescent nanoparticles was adjusted to 20 mg / mL of THF. 50 mL of the solution of photoluminescent nanoparticles are mixed with 0.9 mL of methyl methacrylate (MMA, Sigma Aldrich) with magnetic stirring. In parallel, a solution of 2,2'azobis (2-methylpropionitrile) (AIBN), initiator of radical polymerization, (Sigma Aldrich) was prepared by dissolving 50 mg of AIBN in 5 ml of THF. The AIBN solution was added to the mixture containing the photoluminescent nanoparticles and the final mixture is heated at 70 ° C for 4 h. A dispersion of photoluminescent nanoparticles / PMMA is obtained and can be used for the deposition of photoluminescent particles by ink jet printing. The mass percentage of photoluminescent nanoparticles relative to PMMA is approximately 60%.
    B15141 - Sub-micron phosphors
    权利要求:
    Claims (16)
    [1" id="c-fr-0001]
    1. Method for manufacturing nanoparticles from a photoluminescent material, comprising the following successive steps:
    a) forming nanometric particles (32) of said photoluminescent material;
    b) producing a dispersion containing the particles in a non-aqueous solvent, the dispersion containing, in addition, at least one coupling agent of silane type;
    c) place the dispersion in an autoclave at a pressure between 2 MPa and 100 MPa; and
    d) recover the particles.
    [2" id="c-fr-0002]
    2. Method according to claim 1, in which step b) is preceded by a surface treatment of the nanometric particles (32) with a silica precursor.
    [3" id="c-fr-0003]
    3. Method according to claim 1 or 2, in which the silane coupling agent is an organofunctional compound having the following chemical formula:
    R n SiX 4 _ n where n is equal to 1, 2 or 3, X denotes a hydrolyzable group, and R is a non-hydrolysable organic group.
    [4" id="c-fr-0004]
    4. The method of claim 3, wherein X is an alkoxy group, a halide group or an amine group.
    [5" id="c-fr-0005]
    5. Method according to any one of claims 1 to 4, wherein the non-aqueous solvent is an alcohol.
    [6" id="c-fr-0006]
    6. Method according to any one of claims 1 to 5, wherein step a) comprises grinding particles of said photoluminescent material whose average size is greater than 1 μm to obtain the nanometric particles (32).
    [7" id="c-fr-0007]
    7. The method of claim 6, wherein the particles of said photoluminescent material whose average size is greater than 1 pm are ground in a humid environment.
    [8" id="c-fr-0008]
    8. The method of claim 6, wherein the particles of said photoluminescent material whose average size
    B15141 - Sub-micron phosphors is greater than 1 µm are ground in a solvent different from the non-aqueous solvent used in step b).
    [9" id="c-fr-0009]
    9. Method according to any one of claims 1 to 8, wherein the duration of step c) is between 30 minutes and 48 hours.
    [10" id="c-fr-0010]
    10. Method according to any one of claims 1 to 8, wherein the temperature in the autoclave is between 25 ° C and 300 ° C.
    [11" id="c-fr-0011]
    11. Method according to any one of claims 1 to 10, in which the photoluminescent material is an aluminate, a silicate, a nitride, a fluoride or a sulfide.
    [12" id="c-fr-0012]
    12. The method of claim 11, wherein the photoluminescent material mainly comprises an oxide of yttrium and aluminum or an oxide of lutetium and aluminum containing, in addition, at least one of the following elements: cerium, europium, chromium , neodymium, terbium, dysprosium, praseodymium or gadolinium.
    [13" id="c-fr-0013]
    13. Method according to any one of claims 1 to 12, further comprising, before step c), a step of mixing and treating in the autoclave the nanometric particles in the presence of all or part of the precursors used to form nanoscale particles.
    [14" id="c-fr-0014]
    14. Method according to any one of claims 1 to 13, further comprising, before step c), a step of mixing the nanometric particles with at least one photoluminescent substance (36; 37).
    [15" id="c-fr-0015]
    15. The method of claim 14, wherein the photoluminescent substance is a quantum dot (37).
    [16" id="c-fr-0016]
    16. Method according to any one of claims 1 to 15, in which the nanometric particles (32) are quantum dots.
    B15141
    1/7
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    同族专利:
    公开号 | 公开日
    KR20190042543A|2019-04-24|
    US20190241804A1|2019-08-08|
    FR3053353B1|2018-07-27|
    EP3478794A1|2019-05-08|
    CN109476992A|2019-03-15|
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    WO2018002556A1|2018-01-04|
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    CN103666463B|2012-09-10|2015-06-17|中国石油化工股份有限公司|Fluorescent material, and preparation method and application thereof|
    CN104986726A|2015-02-25|2015-10-21|王建伟|Method for industrial large-scale stable preparation of quantum dots|KR101828214B1|2017-07-18|2018-02-09|성균관대학교산학협력단|Inorganic nanoparticle structure, film, optical member, light-emitting device and quantum dot display apparatus having the same|
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    CN108822266A|2018-05-31|2018-11-16|合肥昂诺新材料有限公司|A kind of preparation method of polyurethane photo-induced luminescent material|
    US11198807B2|2019-09-23|2021-12-14|International Business Machines Corporation|Thermal interface materials with radiative coupling heat transfer|
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    法律状态:
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    2018-05-04| TQ| Partial transmission of property|Owner name: UNIVERSITE CLERMONT AUVERGNE, FR Effective date: 20180403 Owner name: ALEDIA, FR Effective date: 20180403 Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE, FR Effective date: 20180403 Owner name: SIGMA CLERMONT, FR Effective date: 20180403 |
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1656171A|FR3053353B1|2016-06-30|2016-06-30|PROCESS FOR PRODUCING PHOTOLUMINESCENT PARTICLES|
    FR1656171|2016-06-30|FR1656171A| FR3053353B1|2016-06-30|2016-06-30|PROCESS FOR PRODUCING PHOTOLUMINESCENT PARTICLES|
    KR1020197000543A| KR20190042543A|2016-06-30|2017-06-30|Method for producing photoluminescent particles|
    CN201780041220.0A| CN109476992A|2016-06-30|2017-06-30|The method for producing photoluminescent particles|
    EP17745411.3A| EP3478794A1|2016-06-30|2017-06-30|Method for producing photoluminescent particles|
    TW106122031A| TWI735608B|2016-06-30|2017-06-30|Photoluminescent particle manufacturing method|
    PCT/FR2017/051773| WO2018002556A1|2016-06-30|2017-06-30|Method for producing photoluminescent particles|
    US16/309,070| US11198814B2|2016-06-30|2017-06-30|Method for producing photoluminescent particles|
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