CN112877069A - Cr (chromium)3+Doped gallium aluminate near-infrared long-afterglow luminescent material and preparation method thereof - Google Patents
Cr (chromium)3+Doped gallium aluminate near-infrared long-afterglow luminescent material and preparation method thereof Download PDFInfo
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Abstract
The invention discloses Cr3+Gallium aluminate near-infrared long-afterglow luminescent material and a preparation method thereof. The chemical general formula of the near-infrared long afterglow luminescent material is Zn3GaxAl2‑xGeaTibSn2‑a‑ bO10:yCr3+. The preparation method comprises the following steps: weighing raw materials according to the molar ratio of each substance in the equation, adding a fluxing agent, and grinding in an agate mortar to uniformly mix the raw materials to obtain a precursor; loading the precursor into an alumina crucible, and presintering in air or neutral atmosphere; grinding and uniformly mixing the sample obtained by pre-sintering, and calcining in air or neutral atmosphere to obtain Cr3+Gallium aluminate near infrared long afterglow luminescent material. The near-infrared long afterglow fluorescent powder has the advantages of low cost of raw materials, simple and feasible operation, low requirement on equipment and the like. The long afterglow luminescent material has the emission range in the near infrared region, and has the excellent properties of long afterglow time and the like.
Description
Technical Field
The invention relates to near-infrared long-afterglow fluorescent powder and a preparation method thereof, in particular to Cr-containing fluorescent powder3+The doped gallium aluminate near infrared long afterglow luminescent material and its preparation process may be used in indicating illumination and imaging detection, and belongs to the field of long afterglow luminescent material technology.
Background
The long-afterglow luminescent material is one kind of luminescent material capable of absorbing and storing external light radiation energy and releasing light slowly. This characteristic is widely used in indication lighting, such as emergency exit signs, fire-fighting access, architectural decoration, and the like, and recently, is gradually expanded to the application fields of bio-imaging, information storage, and the like. The existing long afterglow materials in the visible light region are mainly divided into blue light, green light and red light materials, wherein the luminous intensity, afterglow time and other optical properties of the blue and green luminescent materials meet the requirements of practical application. However, the luminous intensity and afterglow time of the red long afterglow material are relatively poor, which restricts the application of the material.
In recent years, the near-infrared long afterglow material has attracted much attention in the field of biological imaging, the emitted light is in the near-infrared region (NIR), the molecules emit near-infrared light (700- & ltSUB & gt 1000nm), and the material can be used for detecting living molecular targets, because the blood and tissues of living organisms are relatively transparent in the wavelength range, thereby reducing the problems caused by in vivo background interference. Moreover, compared with other imaging marker materials, the long afterglow material used as the bioluminescent marker material has the unique advantage that the diffusion of the marker material can be observed, which is not possessed by any other marker material. However, the near-infrared long afterglow fluorescent material is lower than the blue and green long afterglow fluorescent materials in both fluorescence intensity and afterglow time, and cannot meet the requirements of practical application. The main reasons are two-fold: one is that the luminous center ions with near infrared luminescence are few (mainly comprising Cr)3+、Mn2 +、Mn4+Etc.), the adjustability of the emission wavelength of the near-infrared long afterglow luminescent material is limited; secondly, the doping of the luminescent center ions is less, so that the property of the long afterglow material is difficult to optimize. Therefore, it is important to find new substrates for long-lasting phosphors. Among the near-infrared long-afterglow materials reported at present, Cr is the most representative3+Doped spinel matrix near-infrared long-afterglow luminescent material ZnGa2O4:Cr3+(Zhang W.W., Zhang, J.Y., Li Y., et al, Applied Surface science 2010,256(14): 4702-. Because of the ZnGa content in the spinel2O4In (3) due to inversion defects of Zn and Ga lattice interchange. Just because the inversion defect plays a role of a trap for storing carriers, the material has better afterglow intensity and afterglow time, but has a large distance from practical application.
Zn3Ga2Ge2O10:Cr3+The material is a novel near-infrared long-afterglow material, and the afterglow time exceeds 360 hours (Pan Z., Lu Y., Liu F., Nature Materials,2012.11(1): 58-63). On the basis, the expensive gallium oxide raw material is replaced by alumina with lower price, similar structure and performance, and the lattice site of Ge is replaced by Ti or (and) Sn at the position of an anion group to regulate and control the luminescent ion Cr3+The surrounding crystal field environment, thereby obtaining the near-infrared long afterglow material with more excellent near-infrared luminescent performance. The gallium aluminate near-infrared long-afterglow fluorescent powder has the advantages of low cost of raw materials, simplicity and feasibility in operation, low requirement on equipment and the like. The long afterglow luminescent material has the emission range in the near infrared region, and has the excellent properties of long afterglow time and the like.
Disclosure of Invention
The technical problem to be solved by the invention is as follows: provides a Cr3+The doped mixed spinel matrix near-infrared long-afterglow luminescent material and the preparation method thereof have the advantages of low cost, simple process and good afterglow performance, can be effectively excited within the range of 300-1200 nm, and the luminescent wavelength range is located in the infrared band between 850-1200 nm.
In order to solve the technical problem, the invention provides Cr3+The gallium aluminate near infrared long afterglow luminescent material is characterized in that the chemical general formula is Zn3GaxAl2-xGeaTibSn2-a-bO10:yCr3+Wherein, 0 < x<1.8,0≤a≤2,0≤b≤2,a+b=2,0.01at%<y<20 at%; the luminescent center is non-rare earth ion Cr3+。
The invention also provides the Cr3+The preparation method of the gallium aluminate near-infrared long-afterglow luminescent material is characterized by comprising the following steps:
step 1): respectively selecting a zinc-containing compound raw material, a gallium-containing compound raw material, an aluminum-containing compound raw material, a germanium-containing compound raw material, a tin-containing compound raw material, a titanium-containing compound raw material and a chromium-containing compound raw material according to a chemical general formula; weighing raw materials according to the molar ratio of each substance in the equation, adding a fluxing agent, and grinding in an agate mortar to uniformly mix the raw materials to obtain a precursor;
step 2): loading the precursor into an alumina crucible, then covering and placing the alumina crucible in a muffle furnace, and presintering the alumina crucible in air or neutral atmosphere;
step 3): taking out the sample obtained by pre-sintering in the step 2), putting the sample into an agate mortar, grinding and uniformly mixing, putting the mixture into an alumina crucible again, and calcining the mixture in air or neutral atmosphere to obtain Cr3+Gallium aluminate near infrared long afterglow luminescent material.
Preferably, in the step 1), the zinc-containing compound raw material is any one or a combination of several of zinc oxide, zinc nitrate, zinc carbonate, zinc hydroxide and zinc oxalate; the gallium-containing compound raw material is any one or combination of more of gallium oxide, gallium nitrate, gallium carbonate, gallium hydroxide and gallium oxalate; the aluminum-containing compound raw material is any one or combination of more of aluminum oxide, aluminum nitrate, aluminum carbonate, aluminum hydroxide and aluminum oxalate; the germanium-containing compound raw material is any one or combination of more of germanium oxide, germanium nitrate, germanium hydroxide and germanium oxalate; the titanium-containing compound raw material is any one or a combination of more of titanium oxide, titanium nitrate, titanium carbonate, titanium hydroxide and titanium oxalate; the tin-containing compound raw material is any one or combination of several of tin oxide, tin nitrate, tin carbonate, tin hydroxide and tin oxalate; the chromium-containing compound raw material is any one or combination of chromium oxide, chromium nitrate, chromium carbonate, chromium hydroxide and chromium oxalate.
Preferably, the fluxing agent in the step 1) is any one or a combination of several of ammonium fluoride, sodium fluoride, lithium fluoride, calcium fluoride, barium fluoride, boric acid, boron trioxide, lithium carbonate and sodium carbonate; the adding amount of the fluxing agent is 0.1-5% of the total mass of the precursor.
Preferably, the temperature of the pre-sintering in the step 2) is 950 ℃, and the temperature is kept for 2 h.
Preferably, the temperature of the calcination in the step 3) is 900-1400 ℃, and the time is 5-30 h.
Cr prepared by the invention3+The gallium aluminate near-infrared long-afterglow luminescent material has wide application in the aspects of indicating illumination, biological imaging, information storage and the like.
Compared with the prior art, the invention has the following beneficial effects:
the near-infrared long afterglow material greatly expands the selectivity of the long afterglow material to the substrate and improves the development space of the near-infrared red afterglow material. The gallium aluminate near-infrared long afterglow material has the advantages of low cost of raw materials, simple and feasible operation, low requirement on equipment and the like. The long afterglow luminescent material has the emission range in the near infrared region, and has the excellent properties of long afterglow time and the like.
Drawings
FIG. 1 is Zn3Ga0.5Al1.5Ge2O10:0.5%Cr3+An X-ray diffraction spectrogram of the near-infrared long-afterglow luminescent material;
FIG. 2 is Zn3Ga0.5Al1.5Ge2O10:0.5%Cr3+Diffuse reflection spectrum of the near-infrared long afterglow luminescent material;
FIG. 3 is Zn3Ga0.5Al1.5Ge2O10:0.5%Cr3+The emission spectrum of the near-infrared long-afterglow luminescent material.
Detailed Description
In order to make the invention more comprehensible, preferred embodiments are described in detail below with reference to the accompanying drawings.
Example 1
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3Ga2Ge2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the germanium oxide and the chromium oxide is 19.0572g, 14.5534g, 16.3302g and 0.0593g respectively. And 0.05 wt% NH was added4F fluxing agent is ground and uniformly mixed by an agate mortar to obtain a precursor, the precursor is added with a proper amount of absolute ethyl alcohol in the agate mortar for uniform grinding, the mixture is placed in a corundum crucible, the temperature is raised to 950 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 2 hours, then the mixture is cooled to room temperature along with a furnace, a sample is placed in the agate mortar, the absolute ethyl alcohol is uniformly ground, the mixture is placed in the corundum crucible, the mixture is heated to 1200 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 10 hours, then the mixture is cooled to room temperature along with the furnace, and the obtained calcined product is crushed and ground to obtain Cr3+Doped Zn3Ga2Ge2O10Near-infrared long afterglow materials.
Example 2
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3Ga1.5Al0.5Ge2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 3.9423g, 2.2579g, 0.4094g, 3.3780g and 0.0123g respectively. And 0.05 wt% NH was added4Grinding and mixing the fluxing agent F with an agate mortar to obtain a precursor, and putting the precursor into the mortarAdding a proper amount of absolute ethyl alcohol into an agate mortar, uniformly grinding, placing the mixture into a corundum crucible, heating to 950 ℃ at the heating rate of 100 ℃/h in the air atmosphere, preserving heat, calcining for 2 hours, cooling to room temperature along with a furnace, placing a sample into the agate mortar, uniformly grinding the absolute ethyl alcohol, placing the sample into the corundum crucible, heating to 1200 ℃ at the heating rate of 100 ℃/h in the air atmosphere, preserving heat, calcining for 10 hours, cooling to room temperature along with the furnace, crushing and grinding the obtained calcined product to obtain Cr3+Doped Zn3Ga1.5Al0.5Ge2O10Near-infrared long afterglow materials.
Example 3
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.0825g, 1.5587g, 0.8480g, 3.4982g and 0.0126g respectively. Adding 0.05 wt% of NH4F fluxing agent is ground and uniformly mixed by an agate mortar to obtain a precursor, the precursor is added with a proper amount of absolute ethyl alcohol in the agate mortar for uniform grinding, the mixture is placed in a corundum crucible, the temperature is raised to 950 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 2 hours, then the mixture is cooled to room temperature along with a furnace, a sample is placed in the agate mortar, the absolute ethyl alcohol is uniformly ground, the mixture is placed in the corundum crucible, the mixture is heated to 1200 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 10 hours, then the mixture is cooled to room temperature along with the furnace, and the obtained calcined product is crushed and ground to obtain Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 4
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3Ga0.5Al1.5Ge2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.2328g, 0.8080g, 1.3187g, 3.6271g and 0.0132g respectively. And 0.05 wt% NH was added4F fluxing agent is ground and uniformly mixed by an agate mortar to obtain a precursor, the precursor is added with a proper amount of absolute ethyl alcohol in the agate mortar for uniform grinding, the mixture is placed in a corundum crucible, the temperature is raised to 950 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 2 hours, then the mixture is cooled to room temperature along with a furnace, a sample is placed in the agate mortar, the absolute ethyl alcohol is uniformly ground, the mixture is placed in the corundum crucible, the mixture is heated to 1200 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 10 hours, then the mixture is cooled to room temperature along with the furnace, and the obtained calcined product is crushed and ground to obtain Cr3+Doped Zn3Ga0.5Al1.5Ge2O10Near-infrared long afterglow materials. The X-ray diffraction spectrum is shown in figure 1, and the X-ray powder diffraction analysis result shows that the obtained fluorescent powder is pure phase. FIG. 2 shows Zn3Ga0.5Al1.5Ge2O10:0.5%Cr3+Diffuse reflection spectrum of the near-infrared long-afterglow luminescent material. FIG. 3 is Zn3Ga0.5Al1.5Ge2O10:0.5%Cr3+Emission spectrum, Zn3Ga1.5Al0.5Ge2O10:0.5%Cr3+The emission peak is about 979nm and is related to Zn3Ga2Ge2O10:0.5%Cr3+Compared with the prior art (as shown in figure 3), the emission peak position is red-shifted by about 50nm, and the luminous intensity is improved by about 20 percent.
Example 5
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.5%Cr3+. The preparation method comprises the following steps:
according toThe molecular formula metering ratio is that zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.0825g, 1.5587g, 0.8480g, 3.4982g and 0.0126g respectively. Adding 0.05 wt% of NH4F fluxing agent is ground and uniformly mixed by an agate mortar to obtain a precursor, the precursor is added with a proper amount of absolute ethyl alcohol in the agate mortar to be ground uniformly, the mixture is placed in a corundum crucible, the temperature is raised to 950 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 2 hours, then the mixture is cooled to room temperature along with a furnace, a sample is placed in the agate mortar, the absolute ethyl alcohol is ground uniformly, the mixture is placed in the corundum crucible, the mixture is heated to 1200 ℃ at the heating rate of 100 ℃/h in the air atmosphere, the mixture is kept warm and calcined for 15 hours, then the mixture is cooled to room temperature along with the furnace, and the obtained calcined product is crushed and ground to obtain Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 6
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.2%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.0825g, 1.5635g, 0.8505g, 3.4983g and 0.0051g respectively. And 0.05 wt% NH was added4F fluxing agent is ground and uniformly mixed by an agate mortar to obtain a precursor, the precursor is added with a proper amount of absolute ethyl alcohol in the agate mortar for uniform grinding, the mixture is placed in a corundum crucible, the temperature is raised to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, the mixture is kept warm and calcined for 2 hours, then the mixture is cooled to room temperature along with a furnace, a sample is placed in the agate mortar, the absolute ethyl alcohol is uniformly ground, the mixture is placed in the corundum crucible, the mixture is heated to 1200 ℃ at the heating rate of 100 ℃/h in an air atmosphere, the mixture is kept warm and calcined for 10 hours, then the mixture is cooled to room temperature along with the furnace, and the calcined product is crushed and ground to obtain the fluxTo Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 7
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.8%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.0822g, 1.5540g, 0.8453g, 3.4981g and 0.0203g respectively. And 0.05 wt% NH was added4F fluxing agent is ground and uniformly mixed by an agate mortar to obtain a precursor, the precursor is added with a proper amount of absolute ethyl alcohol in the agate mortar for uniform grinding, the mixture is placed in a corundum crucible, the temperature is raised to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, the mixture is kept warm and calcined for 2 hours, then the mixture is cooled to room temperature along with a furnace, a sample is placed in the agate mortar, the absolute ethyl alcohol is uniformly ground, the mixture is placed in the corundum crucible, the mixture is heated to 1200 ℃ at the heating rate of 100 ℃/h in an air atmosphere, the mixture is kept warm and calcined for 10 hours, then the mixture is cooled to room temperature along with the furnace, and the obtained calcined product is crushed and ground to obtain Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 8
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.0825g, 1.5587g, 0.8480g, 3.4982g and 0.0126g respectively. And 0.1 wt% NH was added4Grinding and mixing the fluxing agent F with an agate mortar to obtain a precursor, and putting the precursor in the agate mortarAdding a proper amount of absolute ethyl alcohol, uniformly grinding, placing the mixture into a corundum crucible, heating to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, preserving heat and calcining for 2 hours, cooling to room temperature along with a furnace, placing a sample into an agate mortar, uniformly grinding the absolute ethyl alcohol, placing the mixture into the corundum crucible, heating to 1050 ℃ at the heating rate of 100 ℃/h in an air atmosphere, preserving heat and calcining for 10 hours, cooling to room temperature along with the furnace, crushing and grinding the obtained calcined product to obtain Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 9
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide and the chromium oxide is 4.0825g, 1.5587g, 0.8480g, 3.4982g and 0.0126g respectively. Putting the raw material mixture into an agate mortar, uniformly grinding the raw material mixture by absolute ethyl alcohol, putting the raw material mixture into a corundum crucible, heating the mixture to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, preserving heat and calcining for 2 hours, cooling the mixture to room temperature along with a furnace, putting a sample into the agate mortar, uniformly grinding the absolute ethyl alcohol, putting the sample into the corundum crucible, heating the mixture to 1300 ℃ at the heating rate of 100 ℃/h in an air atmosphere, preserving heat and calcining for 10 hours, cooling the mixture to room temperature along with the furnace, crushing and grinding the obtained calcined product to obtain Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 10
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGe2O10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide and oxygen with the purity of more than 99.9 percent are usedGallium oxide, aluminum oxide, germanium oxide and chromium oxide are used as raw materials, and the specific mass of zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide is 4.0825g, 1.5587g, 0.8480g, 3.4982g and 0.0126g respectively. Putting the raw material mixture into an agate mortar, uniformly grinding the raw material mixture by absolute ethyl alcohol, putting the raw material mixture into a corundum crucible, heating the mixture to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, preserving heat and calcining for 2 hours, cooling the mixture to room temperature along with a furnace, putting a sample into the agate mortar, uniformly grinding the absolute ethyl alcohol, putting the sample into the corundum crucible, heating the mixture to 1350 ℃ at the heating rate of 100 ℃/h in an air atmosphere, preserving heat and calcining for 10 hours, cooling the mixture to room temperature along with the furnace, crushing and grinding the obtained calcined product to obtain Cr3+Doped Zn3GaAlGe2O10Near-infrared long afterglow materials.
Example 11
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is in powder form, and the molecular formula is as follows: zn3GaAlGeTiO10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide, the titanium oxide and the chromium oxide is 3.9423g, 1.6261g, 0.8845g, 1.8247g, 1.3927g and 0.0133g respectively. Putting the raw material mixture into an agate mortar, uniformly grinding the raw material mixture by absolute ethyl alcohol, putting the raw material mixture into a corundum crucible, heating the mixture to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, preserving heat and calcining for 2 hours, cooling the mixture to room temperature along with a furnace, putting a sample into the agate mortar, uniformly grinding the absolute ethyl alcohol, putting the sample into the corundum crucible, heating the mixture to 1350 ℃ at the heating rate of 100 ℃/h in an air atmosphere, preserving heat and calcining for 10 hours, cooling the mixture to room temperature along with the furnace, crushing and grinding the obtained calcined product to obtain Cr3+Doped Zn3GaAlGeTiO10Near-infrared long afterglow materials.
Example 12
Cr (chromium)3+The doped gallium aluminate near-infrared long afterglow material is powdered,the molecular formula is as follows: zn3GaAlGeSnO10:0.5%Cr3+. The preparation method comprises the following steps:
according to the molecular formula metering ratio, zinc oxide, gallium oxide, aluminum oxide, germanium oxide and chromium oxide with the purity of more than 99.9 percent are used as raw materials, and the specific mass of the zinc oxide, the gallium oxide, the aluminum oxide, the germanium oxide, the tin oxide and the chromium oxide is 3.7905g, 1.4473g, 0.8845g, 1.6240g, 2.3390g and 0.0118g respectively. Putting the raw material mixture into an agate mortar, uniformly grinding the raw material mixture by absolute ethyl alcohol, putting the raw material mixture into a corundum crucible, heating the mixture to 950 ℃ at the heating rate of 100 ℃/h in a neutral atmosphere, preserving heat and calcining for 2 hours, cooling the mixture to room temperature along with a furnace, putting a sample into the agate mortar, uniformly grinding the absolute ethyl alcohol, putting the sample into the corundum crucible, heating the mixture to 1350 ℃ at the heating rate of 100 ℃/h in an air atmosphere, preserving heat and calcining for 10 hours, cooling the mixture to room temperature along with the furnace, crushing and grinding the obtained calcined product to obtain Cr3+Doped Zn3GaAlGeSnO10Near-infrared long afterglow materials.
Claims (6)
1. Cr (chromium)3+The gallium aluminate near infrared long afterglow luminescent material is characterized in that the chemical general formula is Zn3GaxAl2- xGeaTibSn2-a-bO10:yCr3+Wherein, 0 < x<1.8,0≤a≤2,0≤b≤2,a+b=2,0.01at%<y<20 at%; the luminescent center is non-rare earth ion Cr3+。
2. The Cr of claim 13+The preparation method of the gallium aluminate near-infrared long-afterglow luminescent material is characterized by comprising the following steps:
step 1): respectively selecting a zinc-containing compound raw material, a gallium-containing compound raw material, an aluminum-containing compound raw material, a germanium-containing compound raw material, a tin-containing compound raw material, a titanium-containing compound raw material and a chromium-containing compound raw material according to a chemical general formula; weighing raw materials according to the molar ratio of each substance in the equation, adding a fluxing agent, and grinding in an agate mortar to uniformly mix the raw materials to obtain a precursor;
step 2): loading the precursor into an alumina crucible, then covering and placing the alumina crucible in a muffle furnace, and presintering the alumina crucible in air or neutral atmosphere;
step 3): taking out the sample obtained by pre-sintering in the step 2), putting the sample into an agate mortar, grinding and uniformly mixing, putting the mixture into an alumina crucible again, and calcining the mixture in air or neutral atmosphere to obtain Cr3+Gallium aluminate near infrared long afterglow luminescent material.
3. The Cr of claim 23+The preparation method of the gallium aluminate near-infrared long-afterglow luminescent material is characterized in that in the step 1), the zinc-containing compound raw material is any one or the combination of several of zinc oxide, zinc nitrate, zinc carbonate, zinc hydroxide and zinc oxalate; the gallium-containing compound raw material is any one or combination of more of gallium oxide, gallium nitrate, gallium carbonate, gallium hydroxide and gallium oxalate; the aluminum-containing compound raw material is any one or combination of more of aluminum oxide, aluminum nitrate, aluminum carbonate, aluminum hydroxide and aluminum oxalate; the germanium-containing compound raw material is any one or combination of more of germanium oxide, germanium nitrate, germanium hydroxide and germanium oxalate; the titanium-containing compound raw material is any one or a combination of more of titanium oxide, titanium nitrate, titanium carbonate, titanium hydroxide and titanium oxalate; the tin-containing compound raw material is any one or combination of several of tin oxide, tin nitrate, tin carbonate, tin hydroxide and tin oxalate; the chromium-containing compound raw material is any one or combination of chromium oxide, chromium nitrate, chromium carbonate, chromium hydroxide and chromium oxalate.
4. The Cr of claim 23+The preparation method of the gallium aluminate near-infrared long-afterglow luminescent material is characterized in that the fluxing agent in the step 1) is any one or the combination of more of ammonium fluoride, sodium fluoride, lithium fluoride, calcium fluoride, barium fluoride, boric acid, boron trioxide, lithium carbonate and sodium carbonate; the adding amount of the fluxing agent is 0.1-5% of the total mass of the precursor.
5. The Cr of claim 23+The preparation method of the gallium aluminate near-infrared long-afterglow luminescent material is characterized in that the presintering temperature in the step 2) is 950 ℃, and the temperature is kept for 2 hours.
6. The Cr of claim 23+The preparation method of the gallium aluminate near-infrared long-afterglow luminescent material is characterized in that the calcination temperature in the step 3) is 900-1400 ℃, and the time is 5-30 h.
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113637476A (en) * | 2021-08-19 | 2021-11-12 | 厦门稀土材料研究所 | Rare earth ion co-doped near-infrared long-afterglow luminescent nano material, and preparation method and application thereof |
CN114032092A (en) * | 2021-12-15 | 2022-02-11 | 上海应用技术大学 | Trivalent chromium ion doped near-infrared band luminescent material and preparation method thereof |
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Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108148584A (en) * | 2018-02-05 | 2018-06-12 | 东北大学 | A kind of preparation method of spinel-type gallium zinc germanate spheric granules |
-
2021
- 2021-02-08 CN CN202110180776.6A patent/CN112877069B/en active Active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108148584A (en) * | 2018-02-05 | 2018-06-12 | 东北大学 | A kind of preparation method of spinel-type gallium zinc germanate spheric granules |
Non-Patent Citations (2)
Title |
---|
QIONGYU BAI ET AL.: "Tunable luminescence in co-doped Zn3Al2Ge2O10:Cr3þ by controlling crystal field splitting and nephelauxetic effect", 《JOURNAL OF RARE EARTHS》 * |
杨小平等: "新型近红外超长余辉材料Zn3Al2Ge2O10∶Cr3+的发光性能", 《发光学报》 * |
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