CN109233822B - A yellow long afterglow luminescent material and its preparation method and application - Google Patents
A yellow long afterglow luminescent material and its preparation method and application Download PDFInfo
- Publication number
- CN109233822B CN109233822B CN201811094261.9A CN201811094261A CN109233822B CN 109233822 B CN109233822 B CN 109233822B CN 201811094261 A CN201811094261 A CN 201811094261A CN 109233822 B CN109233822 B CN 109233822B
- Authority
- CN
- China
- Prior art keywords
- luminescent material
- afterglow
- afterglow luminescent
- long afterglow
- yellow long
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000463 material Substances 0.000 title claims abstract description 73
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 8
- 239000000758 substrate Substances 0.000 claims abstract description 7
- 239000012190 activator Substances 0.000 claims abstract description 6
- 229940071182 stannate Drugs 0.000 claims abstract description 5
- 229910008457 SnGe Inorganic materials 0.000 claims abstract 4
- 150000001875 compounds Chemical class 0.000 claims description 23
- 239000000843 powder Substances 0.000 claims description 22
- 239000002994 raw material Substances 0.000 claims description 21
- 239000012298 atmosphere Substances 0.000 claims description 13
- 238000001354 calcination Methods 0.000 claims description 13
- 238000001816 cooling Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 230000005693 optoelectronics Effects 0.000 claims description 3
- 238000005034 decoration Methods 0.000 claims description 2
- 239000002861 polymer material Substances 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 150000002823 nitrates Chemical class 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 239000002341 toxic gas Substances 0.000 abstract description 3
- 239000008204 material by function Substances 0.000 abstract description 2
- 238000000227 grinding Methods 0.000 description 14
- 238000004020 luminiscence type Methods 0.000 description 7
- -1 rare earth ions Chemical class 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 4
- 230000002688 persistence Effects 0.000 description 4
- 229910002651 NO3 Inorganic materials 0.000 description 3
- 238000000137 annealing Methods 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate group Chemical group [N+](=O)([O-])[O-] NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000007873 sieving Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 239000005084 Strontium aluminate Substances 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 238000000295 emission spectrum Methods 0.000 description 2
- 238000004146 energy storage Methods 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 229910052732 germanium Inorganic materials 0.000 description 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 239000012856 weighed raw material Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910003668 SrAl Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- NLQFUUYNQFMIJW-UHFFFAOYSA-N dysprosium(III) oxide Inorganic materials O=[Dy]O[Dy]=O NLQFUUYNQFMIJW-UHFFFAOYSA-N 0.000 description 1
- 230000005264 electron capture Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- 230000005089 fruit drop Effects 0.000 description 1
- 238000011503 in vivo imaging Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/77—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
- C09K11/7707—Germanates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/77—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
- C09K11/7783—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals one of which being europium
- C09K11/7793—Germanates
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Luminescent Compositions (AREA)
Abstract
本发明提供一种黄色长余辉发光材料，涉及新型无机功能材料领域。一种黄色长余辉发光材料，其特征在于，以锗锡酸钡作为发光材料基底，以三价稀土离子Dy3+为激活剂，所述黄色长余辉发光材料的表达式为：Ba1‑xSnGe3O9：xDy3+或Ba1‑x‑ySnGe3O9:xDy3+,yRe；其中，Re选自La3+、Ce3+、Pr3+、Nd3+、Sm3+、Eu3+、Gd3+、Tb3+、Ho3+、Yb3+、Lu3+、Er3+中的一种或多种；0.0005≤x≤0.05，0.0005≤y≤0.05。该材料可发出肉眼可见黄色余辉，具有较强的余辉强度，余辉衰减较慢，余辉持续时间较长。本发明还提供了其制备方法，制备工艺简单、条件易控、设备要求低，制备过程中无有毒气体生成，对环境无污染。
The invention provides a yellow long afterglow luminescent material, which relates to the field of novel inorganic functional materials. A yellow long afterglow luminescent material, characterized in that, using barium germanium stannate as a luminescent material substrate and trivalent rare earth ion Dy 3+ as an activator, the expression of the yellow long afterglow luminescent material is: Ba 1-x SnGe 3 O 9 : xDy 3+ or Ba 1-x-y SnGe 3 O 9 : xDy 3+ , yRe; wherein, Re is selected from La 3+ , Ce 3+ , Pr 3+ , Nd 3+ , Sm 3+ One or more of , Eu 3+ , Gd 3+ , Tb 3+ , Ho 3+ , Yb 3+ , Lu 3+ , Er 3+ ; 0.0005≤x≤0.05, 0.0005≤y≤0.05. The material can emit yellow afterglow visible to the naked eye, with strong afterglow intensity, slower afterglow decay, and longer afterglow duration. The invention also provides a preparation method thereof, the preparation process is simple, the conditions are easy to control, the equipment requirements are low, no toxic gas is generated in the preparation process, and no pollution to the environment.
Description
Technical Field
The invention relates to the field of novel inorganic functional materials, and in particular relates to a yellow long-afterglow luminescent material and a preparation method and application thereof.
Background
Long persistence luminescence (Long persistence luminescence) refers to an optical phenomenon that can continue to emit light for several minutes to several hours after an excitation source is removed, and the process mainly includes energy absorption, energy storage and energy release, i.e., the persistence luminescence stage. The long afterglow phenomenon has been observed and described as early as ancient times, but until recently, the luminescence phenomenon and the luminescence mechanism have been studied. And because of the excellent characteristics of environmental protection, no harm, recycling and the like, the long-afterglow luminescent material has attracted people's attention in recent years, and the research and development thereof are rapidly developed. The long afterglow material is a novel energy storage and electron capture material, can continuously emit light in a low light environment after absorbing energy to capture electrons, is doped with different rare earth ions or transition metal ions and the like, can generate transition of different energy levels to emit light of various wave bands, meets the requirements of different fields, can be applied to the traditional fields of emergency lighting, display and the like, can also be applied to the high-energy ray detection, optical fiber thermometer, nondestructive detection of engineering ceramics, high-density optical storage, display and other high-tech fields, and has potential application value in the fields of in vivo imaging, tumor detection and the like.
To date, a variety of long persistence luminescent materials have been developed that emit light of different colors. For example, SrAl emits green light2O4:Eu2+,Dy3+CaAl emitting blue light2O4:Eu2+,Nd3+Sr for emitting blue light4Al14O25:Eu2+,Dy3+Zn emitting red light3Ga2Ge2O10:Cr3+. Among them, the long afterglow materials having the most excellent properties and being commercially used are SrAl2O4:Eu2+,Dy3 +Because of its strong afterglow intensity and afterglow duration. However, SrAl2O4:Eu2+,Dy3+The chemical property is not stable enough in the air atmosphere, and deliquescence is easy to occur. Therefore, a long-afterglow luminescent material which is stable in chemical property, non-toxic and simple in preparation method is developed in the field, and great driving force is provided for research and application of the material.
Disclosure of Invention
The invention aims to provide a yellow long-afterglow luminescent material which can emit yellow afterglow visible to naked eyes under a low-light environment and has stronger afterglow intensity and afterglow duration.
The invention also aims to provide a preparation method of the yellow long-afterglow luminescent material, which has the advantages of simple preparation process, easily controlled conditions, low equipment requirement, no generation of toxic gas in the preparation process and no pollution to the environment.
The technical problem to be solved by the invention is realized by adopting the following technical scheme.
A yellow long-afterglow luminescent material uses barium germanystinate as base of luminescent material and trivalent rare-earth ion Dy3+The expression of the yellow long afterglow luminescent material as an activator is as follows: ba1-xSnGe3O9：xDy3+Or Ba1-x-ySnGe3O9:xDy3+-yRe; wherein Re is selected from La3+、Ce3+、Pr3+、Nd3+、Sm3+、Eu3+、Gd3+、Tb3+、Ho3+、Yb3+、Lu3+、Er3+One or more of; x is more than or equal to 0.0005 and less than or equal to 0.05, and y is more than or equal to 0.0005 and less than or equal to 0.05.
The invention also provides a preparation method of the yellow long-afterglow luminescent material, which comprises the following steps:
s1, respectively weighing a Ba-containing compound, a Sn-containing compound, a Ge-containing compound, a Dy-containing compound and a Re-containing compound according to the molar ratio of each element in the expression, mixing and grinding the weighed raw materials to obtain raw material powder;
s2, carrying out primary calcination on the raw material powder, cooling and grinding to obtain a pre-sintered sample;
and S3, carrying out secondary calcination on the pre-sintered sample, grinding after cooling, and then sieving to obtain the yellow long-afterglow luminescent material powder.
The yellow long-afterglow luminescent material and the preparation method thereof have the beneficial effects that:
(1) the invention adopts the traditional solid phase method to prepare the long-afterglow luminescent material, has simple preparation process, easily controlled conditions and low equipment requirement, adopts the raw materials of Ba, Sn and Ge which are rich in elements on earth, belongs to green environment-friendly materials, generates no toxic gas in the preparation process and has no pollution to the environment. Compared with common aluminate, the prepared barium germanosuccinate has higher stability and is not easy to deliquesce in atmospheric atmosphere. Therefore, the long afterglow material prepared by using the barium germanium stannate as the substrate has more stable chemical properties.
(2) The yellow long afterglow luminescent material Ba prepared by the invention1-xSnGe3O9：xDy3+After being excited under an ultraviolet lamp for a period of time, the material can emit yellow afterglow visible to the naked eye in a weak light environment, the emission peak is about 580nm, and the material has stronger afterglow intensity, slower afterglow attenuation and longer afterglow duration.
(3) The yellow long afterglow luminescent material Ba prepared by the invention1-x-ySnGe3O9:xDy3+In yRe, Dy3+Co-doping with other different ions, e.g. La3+、Ce3+、Pr3+、Nd3+、Sm3+、Eu3+、Gd3+、Tb3+、Ho3+、Yb3+、Lu3+、Er3+By doping with different elements, the number of carrier traps in the base material is increased or the light emission band of the sample is changed.
(4) The yellow long-afterglow luminescent material prepared by the invention can be mixed with organic high-molecular materials to prepare a film or a resin body, and the film or the resin body is used as a luminescent film or a luminescent device with yellow afterglow, so that the invention lays a foundation for the practical application of the luminescent film in the fields of emergency lighting, photoelectronic devices or elements, instrument display and the like.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings needed to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present invention and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained according to the drawings without inventive efforts.
FIG. 1 is a flow chart of a method for preparing a yellow long-afterglow luminescent material according to an embodiment of the present invention;
FIG. 2 is an X-ray diffraction pattern of the yellow long-afterglow luminescent materials prepared in embodiments 1 to 5 of the present invention;
FIG. 3 is an emission spectrum of a yellow-afterglow long-afterglow luminescent material prepared in example 3 of the present invention;
FIG. 4 shows afterglow spectra of yellow long afterglow phosphors prepared in embodiments 1 to 5 of the material of the present invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available commercially.
The following describes a yellow long afterglow luminescent material and a preparation method thereof according to an embodiment of the present invention.
The embodiment of the invention provides a yellow long-afterglow luminescent material, which takes barium germanium stannate as a luminescent material substrate and trivalent rare earth ions Dy3+The expression of the yellow long afterglow luminescent material as an activator is as follows: ba1-xSnGe3O9：xDy3+Or Ba1-x-ySnGe3O9:xDy3+-yRe; wherein Re is selected from La3+、Ce3+、Pr3+、Nd3+、Sm3+、Eu3+、Gd3+、Tb3+、Ho3+、Yb3+、Lu3+、Er3+One or more of; x is more than or equal to 0.0005 and less than or equal to 0.05, and y is more than or equal to 0.0005 and less than or equal to 0.05. Wherein x and y represent mole percent. The invention takes germanium barium stannate material as a substrate and adopts trivalent rare earth ions Dy3+As an activator, by single doping with Dy3+Form traps in the substrate to trap free electrons, and can also be used for La3+、Ce3+、Pr3+、Nd3+、Sm3+、Eu3+、Gd3+、Tb3+、Ho3+、Yb3+、Lu3+、Er3+With Dy3+And co-doping, wherein the number of carrier traps in the substrate material is increased or the luminescence waveband of a sample is changed through doping of different elements, so that the prepared yellow long-afterglow luminescent material has stronger afterglow intensity and afterglow duration, generates afterglow luminescence visible to the naked eye, and lays a foundation for the practical application of the yellow long-afterglow luminescent material in the fields of emergency lighting, optoelectronic devices or elements, instrument display and the like.
Further, the ratio of x to y is 1: 0.5-1.5. More preferably, the ratio of x and y is 1: 1. The ratio of x and y is controlled to ensure that Dy with sufficient concentration is present3+Ions, as activators and luminescent centers. Avoid the excessive Re element, the impure prepared long afterglow material and the luminous efficiency of the long afterglow materialThe fruit drops. Wherein the optimal proportion of x is 0.02.
The embodiment of the invention also provides a preparation method of the yellow long-afterglow luminescent material, which comprises the following steps:
s1, respectively weighing a Ba-containing compound, a Sn-containing compound, a Ge-containing compound, a Dy-containing compound and a Re-containing compound according to the molar ratio of each element in the expression, mixing and grinding the weighed raw materials to obtain raw material powder.
Further, in step S1, each of the raw materials is selected from an oxide containing a corresponding element, a salt, or a mixture of both; wherein the salt is selected from nitrate and/or carbonate. In a preferred embodiment of the present invention, the Ba-containing compound is selected from an oxide, a nitrate or a carbonate thereof, the Sn-and Ge-containing compound is selected from an oxide thereof, and the Dy-and Re-containing compound is selected from an oxide or a nitrate thereof.
Preferably, in the embodiment of the present invention, BaCO is selected3、SnO2、GeO2、Dy2O3The raw materials are easily available and relatively inexpensive as raw materials for synthesis. And Ba, Sn and Ge are rich elements on earth, and belong to green environment-friendly materials, and the prepared finished product has no pollution to the environment.
Further, in step S1, the grinding step is: and mixing the Ba-containing compound, the Sn-containing compound, the Ge-containing compound, the Dy-containing compound and the Re-containing compound, adding a solvent, and grinding for 1-4 h. Wherein the solvent is absolute ethyl alcohol, water or a mixture of the absolute ethyl alcohol and the water. The raw materials are mixed and ground, so that the elements are uniformly distributed, and the full reaction in the subsequent steps is facilitated. The ethanol or water is added for grinding, so that the grinding is more uniform, and the raw materials do not react.
And S2, carrying out primary calcination on the raw material powder, cooling and grinding to obtain a pre-sintered sample.
Heating the raw material powder to 700-1000 ℃ at a speed of 1-10 ℃/min under an air atmosphere, firing for 2-4 hours, cooling to 200-500 ℃ at a cooling rate of 5-15 ℃/min, and naturally cooling to room temperature along with the furnace to obtain the pre-sintered sample.
Further, heating the raw material powder to 750-850 ℃ at a speed of 2-5 ℃/min in an air atmosphere, and burning for 2-4 hours to obtain the pre-sintered sample. The temperature rise speed is controlled, so that the raw materials are prevented from being reacted unevenly due to overlarge temperature difference. More preferably, the temperature is raised at a rate of 5 ℃/min.
Furthermore, the temperature is reduced to 200-300 ℃ at a rate of 10-15 ℃/min, and then the mixture is naturally cooled to room temperature along with the furnace. The annealing temperature is controlled, so that the reaction temperature is reduced rapidly, the experimental time is shortened, and the continuous sintering growth of the product in the annealing process due to overlong annealing time is avoided.
And S3, carrying out secondary calcination on the pre-sintered sample, grinding after cooling, and then sieving to obtain the yellow long-afterglow luminescent material powder.
Further, in step S3, the second calcination step is: and heating the pre-sintered sample to 1200-1400 ℃ at a speed of 1-10 ℃/min in an air atmosphere, and firing for 3-8 hours.
Further, the raw material powder is heated to 1200-1400 ℃ at a speed of 4-8 ℃/min in the air atmosphere, and is burned for 5-8 hours. The above conditions make the reaction more complete and do not make the temperature rise process too slow.
The method of calcining firstly, grinding secondly and calcining secondly is adopted, so that the sintering growth of the product in the calcining process can be inhibited, the full reaction in the calcining process is ensured, the prepared product has pure components, and the prepared long afterglow luminescent material powder is more exquisite. And the atmosphere of the two-time calcination is only air atmosphere, and the valence-change reaction does not occur in the reaction process, so that the method has lower cost and more advantages compared with the prior art of calcining in reducing atmosphere.
Further, in step S3, the mesh number of the screen is 20-50 meshes. And filtering the prepared powder by using a screen to ensure that the particle size of the prepared long-afterglow luminescent material powder is consistent, uniform and fine.
Further, the method also comprises the step of sealing the yellow long-afterglow luminescent material powder:
s4, mixing the yellow long afterglow luminescent material powder and organic high polymer material to obtain the film or resin body. The prepared yellow long-afterglow luminescent material powder can be mixed with organic high-molecular materials such as silica gel and resin to prepare a film or a resin body, so that the transmission and storage of light energy are realized.
The embodiment of the invention provides a yellow long-afterglow luminescent material which can emit light in an afterglow form in a dark place under the excitation of an ultraviolet lamp, and the afterglow luminescent intensity can be observed by naked eyes. And the afterglow attenuation is slow, and the afterglow emission time can last for hours. The characteristics can lead the yellow long afterglow luminescent material to be applied to the fields of night emergency indicating devices, optoelectronic devices, instrument display devices, illuminating devices, home decorations and the like.
The features and properties of the present invention are described in further detail below with reference to examples.
Examples 1 to 6
(1) the raw materials of each element are weighed according to the following table and mixed, and absolute ethyl alcohol is added for full grinding for 3 hours, so that raw material powder is obtained.
(2) Placing the raw material powder into a high-temperature tube furnace, heating to 800 ℃ at the speed of 5 ℃/min under the air atmosphere, burning for 2 hours, then cooling to 200 ℃ at the speed of 10 ℃/min, and then naturally cooling to room temperature along with the furnace to obtain a pre-sintered sample.
(3) And after the pre-sintered sample is cooled to room temperature, taking out and fully grinding, putting the pre-sintered sample into the high-temperature tube furnace again, heating to 1300 ℃ at the speed of 7 ℃/min in the air atmosphere, firing for 4 hours, and naturally cooling to room temperature along with the furnace.
(4) And (4) grinding the cooled sample again, and sieving the ground sample by using a 20-50-mesh sieve to obtain the yellow long-afterglow luminescent material.
(5) The yellow long afterglow luminescent material powder is put into a transparent test tube and is excited by ultraviolet light to test the optical performance of the test tube.
The lowest vertical line in the figure is pure phase BaSnGe3O9The diffraction peak and pure phase BaSnGe of the yellow long afterglow luminescent material prepared in the embodiments 1 to 53O9The diffraction peak of the doped Dy is kept consistent, and the doped Dy is not detected3+Other phases of the rare earth ions show that the prepared sample has the characteristic of high purity and is doped with the rare earth ions Dy3+The crystal structure is not disturbed.
FIG. 3 is the emission spectrum of the yellow-afterglow long-afterglow luminescent material prepared in example 3 of the present invention. It can be seen that the emission peaks at 490nm, 580nm and 680nm are Dy3+Thereby showing Dy3+In the luminescent material base, as luminescent centers.
FIG. 4 shows afterglow spectra of yellow long afterglow phosphors prepared in embodiments 1 to 5 of the material of the present invention. As can be seen from the figure, the afterglow emission peaks of examples 1 to 5 are around 580nm, which shows yellow afterglow, and are Dy3+Is/are as follows4F9/2To6H13/2And (4) energy level transition. And examples 1 to 5 all had strong afterglow emission intensity. Among them, the remaining luminance emission intensity is strongest in example 3 compared with other examples.
The embodiments described above are some, but not all embodiments of the invention. The detailed description of the embodiments of the present invention is not intended to limit the scope of the invention as claimed, but is merely representative of selected embodiments of the invention. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Claims (6)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201811094261.9A CN109233822B (en) | 2018-09-19 | 2018-09-19 | A yellow long afterglow luminescent material and its preparation method and application |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201811094261.9A CN109233822B (en) | 2018-09-19 | 2018-09-19 | A yellow long afterglow luminescent material and its preparation method and application |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN109233822A CN109233822A (en) | 2019-01-18 |
| CN109233822B true CN109233822B (en) | 2021-05-14 |
Family
ID=65059726
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201811094261.9A Expired - Fee Related CN109233822B (en) | 2018-09-19 | 2018-09-19 | A yellow long afterglow luminescent material and its preparation method and application |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN109233822B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115340864B (en) * | 2022-09-15 | 2023-08-25 | 厦门理工学院 | Red luminescent material and preparation method and application thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103131415A (en) * | 2013-03-05 | 2013-06-05 | 中山大学 | Yellow long-lasting phosphor material and preparation method thereof |
| CN106497555A (en) * | 2016-11-01 | 2017-03-15 | 兰州大学 | Long persistence luminescent silicate material and preparation method thereof |
-
2018
- 2018-09-19 CN CN201811094261.9A patent/CN109233822B/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103131415A (en) * | 2013-03-05 | 2013-06-05 | 中山大学 | Yellow long-lasting phosphor material and preparation method thereof |
| CN106497555A (en) * | 2016-11-01 | 2017-03-15 | 兰州大学 | Long persistence luminescent silicate material and preparation method thereof |
Non-Patent Citations (2)
| Title |
|---|
| LUMINESCENCE OF BaSnSi309:Ti4+ COMPARED TO BaZrSi309:Ti4+;W. L. Konijnendijk;《Inorganic and Nuclear Chemistry Letters》;20030520;第17卷(第5-6期);第129-132页 * |
| Luminescence properties of long persistent phosphors BaZrSi3O9: R3+ (R = Eu, Sm, Dy, Tb and Pr) based on host sensitization;Yahong Jin等;《Optical Materials》;20140226;第36卷;第1814-1818页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN109233822A (en) | 2019-01-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN113214823B (en) | A kind of ternary metal sulfide oxide with both long afterglow and electroluminescence and preparation method thereof | |
| CN113817465A (en) | A kind of bismuth ion doped germanate-based orange long afterglow material and preparation method thereof | |
| CN111234814B (en) | A kind of Mn4+ doped oxynitride red phosphor and preparation method thereof | |
| CN103160278A (en) | Red long-lasting phosphor material and preparation method thereof | |
| CN107974250B (en) | A blue-green silicate ultra-long afterglow luminescent material and preparation method thereof | |
| CN109536165B (en) | A kind of germanate long afterglow luminescent material and preparation method thereof | |
| CN107418571B (en) | Mn (manganese)2+Doped yellow long-afterglow luminescent material and preparation method thereof | |
| JP5039706B2 (en) | Long afterglow luminescent material and method for producing the same | |
| CN101974324A (en) | Ultra-long afterglow silicate long afterglow phosphors and preparation method thereof | |
| CN109233822B (en) | A yellow long afterglow luminescent material and its preparation method and application | |
| CN100386405C (en) | Red long afterglow luminescent material and its prepn | |
| EP2565253B1 (en) | Silicate luminescent material and production method thereof | |
| CN110437828B (en) | A kind of green long afterglow luminescent material and preparation method thereof | |
| CN113481001A (en) | Copper ion doped gallate-based red long-afterglow material and preparation method thereof | |
| US3509064A (en) | Alkaline earth tellurate phosphors | |
| JP5780573B1 (en) | Phosphorescent phosphor | |
| CN111100634A (en) | Long-afterglow fluorescent material and preparation method thereof | |
| CN103224788B (en) | Red fluorescent luminescent material and preparation method thereof | |
| CN106147767B (en) | A kind of long after glow luminous material and preparation method thereof | |
| CN114106829A (en) | A kind of Mn2+ doped red light long afterglow luminescent material and preparation method thereof | |
| CN113528130A (en) | A kind of europium and neodymium co-doped borate yellow long afterglow luminescent material and preparation method thereof | |
| JP2014523952A (en) | Phosphor precursor composition | |
| CN109266335B (en) | Yellow long-afterglow luminescent material and preparation method thereof | |
| US8686626B2 (en) | Oxynitride-based phosphor and light emitting device including the same | |
| CN107652972B (en) | Color-adjustable self-activated long afterglow material and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20210514 |