CN115109582A - Red light-near infrared light LED device and application thereof - Google Patents

Red light-near infrared light LED device and application thereof Download PDF

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CN115109582A
CN115109582A CN202210647795.XA CN202210647795A CN115109582A CN 115109582 A CN115109582 A CN 115109582A CN 202210647795 A CN202210647795 A CN 202210647795A CN 115109582 A CN115109582 A CN 115109582A
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near infrared
red
led device
light
fluorescent powder
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CN115109582B (en
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陈雷
蒋婷
刘琦
吴亚兵
杨书淇
王泽飞
王勇
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Intelligent Manufacturing Institute of Hefei University Technology
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Abstract

The invention belongs to the field of LED device preparation, and discloses a red light-near infrared light LED device and application thereof. The LED device is prepared by mixing red light-near infrared light fluorescent powder, transparent silica gel and optional red light fluorescent powder and packaging by a packaging process; the chemical formula of the red light-near infrared light fluorescent powder is as follows: li (M) 1‑x Cr x )O 2 Wherein M is at least one of Sc, Al, Ga, In, Lu, Be, Mg, Si and Ge, 0<x<0.10. According to the inventionThe red light-near infrared light LED device can be used for treating gastrointestinal diseases, neurological diseases, juvenile myopia and other probiotic supplement related diseases, and can also be used in other occasions requiring red light-near infrared light.

Description

Red light-near infrared light LED device and application thereof
Technical Field
The invention belongs to the field of LED device preparation, and particularly relates to a red light-near infrared light LED device and application thereof.
Background
Since the market popularization of white light LED lighting started in 2011, the application of LEDs in the fields of home and office lighting, photosynthetic agriculture and plant factories, ultraviolet sterilization, industrial curing and the like makes a great breakthrough, new applications need to be developed in the future development of the LED industry, the manufacturing technology of visible light and ultraviolet band LED devices is improved day by day, and one direction with a great development prospect is biomedical science. With the innovation of light source technology, light sources for phototherapy are no longer limited to lasers, and the same effect as lasers can be achieved by using LEDs. In the field of academia, the latest technology for disease treatment by light is called Photobiomodulation (PBM). Both PBM and LLLT (low dose laser therapy) utilize photon or photonic means for disease treatment.
Previous LLLT studies have shown that using a combination of wavelengths works better than using a single wavelength, mainly because the laser used in LLLT is linear light, while the absorption spectrum of biological tissue tends to be broadband. The laser light source is used in phototherapy, and the defects of limited selectable wavelength, narrow coverage wavelength range and the like exist. In addition, laser equipment is complex and expensive. The LED light source utilizing fluorescence conversion is a continuous broadband spectrum, which is beneficial to overcoming the defect of LLLT linear light. Compared with laser, the solid-state LED light source has the remarkable advantages of small size, high reliability, portability, low cost and the like.
Parkinson's Disease (PD) and Alzheimer's Disease (AD) are two common neurodegenerative diseases of the elderly, seriously jeopardizing human life health and reducing quality of life. Typical symptoms of PD patients are unique motor deficits including tremor, rigidity, akinesia, and postural instability, often associated with the loss of dopaminergic cells of the substantia nigra pars compacta. Typical symptoms of AD patients are cognitive deficits, the main pathological features being synapses and neuronal degeneration as well as amyloid plaques and neurofibrillary tangles. In addition, mitochondrial dysfunction appears in PD and AD patients in the early and late stages of the disease. At present, the medical community adopts medicines for treating two diseases, but the method can only relieve the symptoms of patients and cannot prevent or further prevent the neuronal degeneration. Numerous studies have shown that PBM can promote neurons to release dopamine, a neurotransmitter capable of producing a large amount of ATP and increasing mitochondrial activity, and is considered as a final measure capable of fundamentally treating neurodegenerative diseases.
In addition to the typical pathological symptoms described above, another major symptom of PD and AD patients is intestinal dysfunction, often with symptoms of intestinal dysfunction in PD patients that are earlier than their typical motor deficit characteristics. The "brain-gut axis" mechanism is a widely accepted view of the pathogenesis of neurological diseases at present, i.e. the gut nervous system connects the gut to the central nervous system via nervous, hormonal and immunological signals, and the gut microbiome is an important signal source. Thus, one of the current ways to treat neurological disorders is to take probiotics and achieve positive therapeutic effects.
The influence of light on cellular energy metabolism is a commonly recognized action mechanism of PBM, and particularly, light acts on Cytochrome C Oxidase (CCO) in mitochondria to increase the permeability of the mitochondrial membrane, the active oxygen is transiently increased, a mitochondrial signal pathway related to neuroprotection and cell survival is activated, nitric oxide released by photodissociation of CCO and synthesis of CCO can stimulate vasodilation and blood flow, and ATP production is promoted by increasing oxygen consumption.
Light not only affects cellular metabolism, but also can modulate microbial activity. In addition to taking drugs that alleviate typical pathologies, an important strategy for PD, AD treatment is to modulate the patient's intestinal microbial profile according to the "brain-gut axis" mechanism, where lactic acid bacteria, as a typical probiotic, are of great significance for PD, AD treatment. Therefore, the PBM method is adopted to regulate the microorganisms in the brain-intestinal axis, is hopeful to complement the conventional medicine and surgical treatment, and has positive treatment effect on the neurological diseases.
The pathogenesis of myopia is unknown, and the mainstream view is that the elongation of the axis of the axio-myopic eye is controlled by the neurotransmitter dopamine, and secondly is related to fundus and sclera hypoxia. The use of PBMs to stimulate the release of the neurotransmitter dopamine from retinal dopamine neurons and to reduce oxidative stress damage has been demonstrated in our studies. PBM is considered to be the ultimate measure that will eventually overcome the myopia problem in humans.
At present, the blue light LED chip has mature technical process and reliable raw materials, and MOVCD equipment for growing the blue light chip is abundant, but the conversion of the 450-plus 480nm blue light emitted by the LED chip into the 850-nm red light-near infrared light with the peak wavelength of 800-plus is a great challenge due to the huge Stokes shift. Suitable luminescent centers are Cr 3+ 、Eu 2+ However, Eu 2+ The near infrared luminescence is mainly caused by defect luminescence, but the defect thermal stability is poor, so that the method is not suitable for industrial application.
Therefore, it is urgent to provide a new red-near infrared LED device to meet the requirements of non-invasive PBM treatment of neurological diseases and myopia PBM treatment for light sources.
Disclosure of Invention
The invention aims to provide a red light-near infrared light LED device aiming at the defects of the prior art. The red light-near red light LED device can be used for treating gastrointestinal diseases, neurological diseases, juvenile myopia and other probiotic supplement related diseases.
In order to achieve the above object, a first aspect of the present invention provides a red-near infrared LED device, which is prepared by mixing red-near infrared phosphor, transparent silica gel, and optionally red phosphor, and encapsulating the mixture by an encapsulation process;
the chemical formula of the red light-near infrared light fluorescent powder is as follows: li (M) 1-x Cr x )O 2 Wherein M is at least one of Sc, Al, Ga, In, Lu, Be, Mg, Si and Ge, 0<x<0.10。
According to the present invention, preferably, the red-near infrared phosphor has a chemical formula of: li [ A ] 1-x-2z (B z C z )]Cr x O 2 Wherein A is at least one of Sc, Al, Ga, In and Lu, B is Be and/or Mg, C is Si and/or Ge, 0<x<0.10,0<z<0.01。
According to the present invention, it is preferable that the raw material containing the element M is at least one of an oxide, a nitrate, an oxalate, and a carbonate containing the element M.
According to the present invention, preferably, the raw material containing the element a is at least one of an oxide, a nitrate, an oxalate, and a carbonate containing the element a.
According to the present invention, it is preferable that the raw material containing the element B is at least one of an oxide, a nitrate, an oxalate, and a carbonate containing the element B.
According to the present invention, preferably, the raw material containing the element C is at least one of an oxide, a nitrate, an oxalate, and a carbonate containing the element C.
According to the present invention, preferably, the red-near infrared phosphor has a chemical formula of: li (Sc) 1-x-y Ga y )Cr x O 2 Wherein 0 is<y<1。
According to the present invention, preferably, the red-near infrared phosphor has a chemical formula of: li (Sc) 1-x-m Al m )Cr x O 2 Wherein 0 is<m<1。
According to the present invention, preferably, the preparation method of the red-near infrared phosphor comprises:
the first step is as follows: will contain Cr 3+ Grinding and mixing the raw material containing the element M and the fluxing agent uniformly, and carrying out primary calcination, dehydration, degassing and removal of surface adsorbed substances to obtain a first-step product;
the second step is that: and grinding the product obtained in the first step, then carrying out secondary calcination, crushing, grinding, washing, filtering and drying to obtain the red light-near infrared light fluorescent powder.
According to the present invention, preferably, the operating conditions of the first calcination include: heating to 300 ℃ at a speed of 3-10 ℃/min in air, preserving heat for 0.3-2 hours, heating to 1000 ℃ at a speed of 3-10 ℃/min, preserving heat for 1-3 hours, cooling to 350 ℃ at a speed of 250 ℃ at a speed of 5-10 ℃/min, cutting off power, and cooling to 25-30 ℃ with the furnace.
According to the present invention, preferably, the operating conditions of the second calcination include: heating to 900 ℃ at a speed of 3-10 ℃/min in the air, preserving heat for 0.5-1.5 hours, heating to 1100-.
According to the invention, the addition amount of the fluxing agent is preferably 1.5-3.5% of the total mass of the raw materials used for preparing the red-near infrared fluorescent powder.
According to the present invention, preferably, the flux is at least one of aluminum fluoride, barium fluoride, ammonium chloride, ammonium fluoride, ammonium bifluoride, and boric acid, and preferably, the flux is boric acid.
According to the invention, the ratio of the dosage of the red light-near infrared light fluorescent powder to the dosage of the red light fluorescent powder to the dosage of the transparent silica gel is preferably (1-3): 0-0.1): 1.
According to the present invention, the red phosphor has a chemical formula of (Ca, Sr) AlSiN 3 :Eu 2+ Or is Q 2 Si 5 N 8 :Eu 2+ Wherein Q is at least one of Sr, Ca, Ba and Mg.
According to the present invention, preferably, the packaging process includes: and (3) defoaming and degassing a mixture of the red light-near infrared light fluorescent powder, the transparent silica gel and the optional red light fluorescent powder, titrating the mixture on a blue light LED chip, and baking and curing to obtain the red light-near infrared light LED device.
According to the invention, the emission wavelength peak of the blue LED chip is preferably 400-500 nm.
According to the invention, preferably, the emission wavelength range of the red-near infrared light LED device is 700-950nm, and the emission wavelength peak value is 813-835 nm.
The invention provides application of the red light-near infrared light LED device as a light source for treating gastrointestinal diseases, neurological diseases and juvenile myopia. In the invention, the red light-near infrared light LED device is used as a light source manufactured by using the device and medical instruments and equipment manufactured by using the device and a light-emitting device. The application of the invention, including but not limited to medical instruments and equipment, can also be other applications developed by using the near-infrared LED device manufactured by the invention.
The technical scheme of the invention has the following beneficial effects:
(1) the red light-near infrared light fluorescent material used by the invention has a perovskite-like crystal structure, the high-symmetry substrate is beneficial to improving the luminous efficiency, the emission wavelength range is 700-950nm, the emission wavelength peak value is adjustable within 813-835nm, the whole spectrum red shift of the encapsulated LED device is 50-150nm, and the encapsulated LED device has the potential of photobiotherapy application; two excitation bands are arranged at 400-800nm, and can be effectively excited by blue light; the absorptivity and internal and external quantum efficiency of the red light-near infrared light fluorescent material are respectively 40.9%, 34.5% and 14.1%.
(2) Compared with a laser light source, the light source generated by the red light-near infrared light LED device has the remarkable advantages of low cost, portability and the like, particularly, the emission spectrum of the light source is a wide band spectrum and is consistent with the wide band absorption of a light receptor in an organism, and compared with the linear light of the laser light source, the light source is more suitable for PBM.
(3) The red light-near infrared light LED device has the photoelectric conversion efficiency of 7.92% under the drive current of 20 mA.
(4) The red light-near infrared light LED device can be used for medical light sources and equipment, treating gastrointestinal diseases, nervous diseases (stimulating secretion and growth of dopamine and neurons, having important significance for prevention, control and treatment of the nervous diseases and complications such as Parkinson's disease and Alzheimer's disease) and other probiotic supplementation related diseases, and can also be used for other purposes.
(5) The research of using the red light-near infrared light LED device to carry out light irradiation on the lactobacillus to adjust the activity shows positive influence, and further proves the important reference value of the device for adjusting the brain-intestine axis of the nervous diseases.
(6) The light source emitted by the red light-near infrared light fluorescent material can promote the growth of intestinal lactobacillus of the organism, promote the expression of anti-inflammatory factors and promote the balance of intestinal flora in the organism by regulating the activity of cells in the organism, and has prevention, control and treatment effects on preventing and treating nervous diseases such as Parkinson's disease and Alzheimer's disease.
Additional features and advantages of the invention will be set forth in the detailed description which follows.
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The above and other objects, features and advantages of the present invention will become more apparent by describing in detail exemplary embodiments thereof with reference to the attached drawings, wherein like reference numerals generally represent like parts in the exemplary embodiments of the present invention.
FIG. 1 shows the emission spectra of red-near infrared phosphors provided in examples 1-5 of the present invention.
FIG. 2 shows the excitation spectra of red-NIR phosphors provided in examples 1-5 of the present invention.
FIG. 3 shows the emission spectra of red-NIR phosphors provided in examples 6-9 of the present invention.
FIG. 4 shows the excitation spectra of red-NIR phosphors provided in examples 6-9 of the present invention.
FIG. 5 shows the emission spectra of red-NIR phosphors provided in examples 10-13 of the present invention.
FIG. 6 shows the excitation spectra of red-NIR phosphors provided in examples 10-13 of the present invention.
FIG. 7 shows emission spectra of red-near infrared phosphors provided in examples 14-16 of the present invention.
FIG. 8 shows the excitation spectra of red-NIR phosphors provided in examples 14-16 of the present invention.
FIG. 9 shows the emission spectra of red-near infrared phosphors provided in examples 17-20 of the present invention.
FIG. 10 shows the excitation spectra of red-NIR phosphors provided in examples 17-20 of the present invention.
FIG. 11 shows emission spectra of red-near infrared phosphors provided in examples 21-25 of the present invention.
FIG. 12 shows the excitation spectra of red-NIR phosphors provided in examples 21-25 of the present invention.
FIG. 13 shows the emission spectra of red-NIR phosphors provided in examples 26-30 of the present invention.
FIG. 14 shows the excitation spectra of red-NIR phosphors provided in examples 26-30 of the present invention.
FIG. 15 shows XRD patterns of red-near infrared phosphors provided in examples 26-30 of the present invention.
FIG. 16 shows an emission spectrum of a red-near infrared phosphor provided in example 31 of the present invention.
Fig. 17 shows an excitation spectrum of the red-near infrared phosphor provided in example 31 of the present invention.
Fig. 18 shows emission spectra of a red-near infrared LED device provided in embodiment 32 of the present invention under different direct current driving conditions.
Fig. 19 shows a photoelectric conversion efficiency and a light output power curve of a red-near infrared LED device according to embodiment 32 of the present invention as a function of current.
FIG. 20 is a graph showing the comparison of the red-near infrared LED device of example 32 of the present invention with the DNA synthesis rate, the absorption spectrum of cytochrome C oxidase.
FIGS. 21(a) - (b) show the growth of lactic acid bacteria after 24h culture (no light (a) and 720nm light (b)) in the test examples of the present invention.
Detailed Description
Preferred embodiments of the present invention will be described in more detail below. While the following describes preferred embodiments of the present invention, it should be understood that the present invention may be embodied in various forms and should not be limited by the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.
In the following examples, the raw materials used to prepare the red-near infrared phosphor include:
MgO(98.5%)、Sc 2 O 3 (99.99%)、Ga 2 O 3 (99.99%)、Cr 2 O 3 (99.99%)。Li 2 CO 3 (99.99%) and Al 2 O 3 (99.99%)。
Examples 1 to 5
Examples 1-5 provide red-near infrared phosphors having the formula: li (M) 1-x Cr x )O 2 Wherein M is Sc (x ═ 0.06), Al (x ═ 0.06), Ga (x ═ 0.06), In (x ═ 0.06), Lu (x ═ 0.06), respectively.
The preparation method of the red light-near infrared light fluorescent powder comprises the following steps:
the first step is as follows: will contain Cr 3+ Grinding and mixing the raw material containing the element M and the fluxing agent uniformly, and carrying out primary calcination, dehydration, degassing and removal of surface adsorbed substances to obtain a first-step product;
the second step: and grinding the product obtained in the first step, then carrying out secondary calcination, crushing, grinding, washing, filtering and drying to obtain the red light-near infrared light fluorescent powder.
The operating conditions of the first calcination include: heating to 176 ℃ at a speed of 5 ℃/min in the air, preserving heat for 2 hours, heating to 900 ℃ at a speed of 5 ℃/min, preserving heat for 2 hours, cooling to 300 ℃ at a speed of 5 ℃/min, powering off, and cooling to 25 ℃ along with the furnace;
the operating conditions of the second calcination include: heating to 900 deg.C at 5 deg.C/min in air, holding for 1 hr, heating to 1100 deg.C at 5 deg.C/min, holding for 6 hr, cooling to 900 deg.C at 5 deg.C/min, holding for 0.5-2 hr, cooling to 300 deg.C at 5 deg.C/min, cutting off power, and cooling to 25 deg.C with the furnace.
The fluxing agent is boric acid, and the addition amount of the boric acid is 2.5% of the total mass of the raw materials used for preparing the red light-near infrared light fluorescent powder.
The emission spectrum and excitation spectrum of the red-near infrared phosphors of examples 1 to 5 are shown in FIGS. 1 and 2. As is clear from FIGS. 1 and 2, Li (Al) in example 2 0.94 Cr 0.06 )O 2 And Li (Ga) of example 3 0.94 Cr 0.06 )O 2 Due to [ MO ] 4 ]The tetrahedral structure and the excessive difference of the ionic radii can not realize Cr 3+ Thus, the red-near infrared phosphor that gives the best emission is the Li (Sc) of example 1 0.94 Cr 0.06 )O 2
Examples 6 to 9
Examples 6 to 9 provide a red-near infrared phosphor Li (Sc) 0.94 Cr 0.06 )O 2 Examples 6-9 differ from example 1 only in that: the second temperature rise in the second calcination operation is different, and is 1200 ℃, 1250 ℃, 1300 ℃ and 1350 ℃.
The emission spectrum and excitation spectrum of the red-near infrared phosphors of examples 6 to 9 are shown in FIGS. 3 and 4. As can be seen from fig. 3 and 4, the optimum temperature for the second temperature increase in the second calcination operation is 1250 ℃.
Examples 10 to 13
Examples 10-13 provide Red-near Infrared phosphor Li (Sc) 0.94 Cr 0.06 )O 2 Examples 10-13 differ from example 7 only in that: the fluxing agent is aluminum fluoride, barium fluoride, ammonium fluoride and boric acid, and the addition amounts of the aluminum fluoride, the barium fluoride, the ammonium fluoride and the boric acid are respectively and independently 2.0 percent of the total mass of the raw materials for preparing the red light-near infrared light fluorescent powder.
The emission spectra and excitation spectra of the red-near infrared phosphors of examples 10-13 are shown in FIGS. 5 and 6. As is clear from FIGS. 5 and 6, the most preferable flux is boric acid of example 13.
Examples 14 to 16
Examples 14 to 16 provide Red-near Infrared phosphor Li (Sc) 0.94 Cr 0.06 )O 2 Examples 14-16 differ from example 13 only in that: adding 2.0% boric acid as fluxing agent, the second timeThe heat preservation time when the temperature is raised to 1250 ℃ for the second time in the calcination operation is different and is respectively 4h, 8h and 10 h.
The emission spectra and excitation spectra of the red-near infrared phosphors of examples 14-16 are shown in FIGS. 7 and 8. As is clear from fig. 7 and 8, the optimum temperature retention time for the second temperature rise in the second firing operation was 8 hours in example 15.
Examples 17 to 20
Examples 17 to 20 provide a red-near infrared phosphor Li (Sc) 0.94 Cr 0.06 )O 2 Examples 17-20 differ from example 15 only in that: the boric acid accounts for 1.5 percent, 2.5 percent, 3 percent and 3.5 percent of the total mass of the raw materials used for preparing the red light-near infrared light fluorescent powder respectively.
The emission spectra and excitation spectra of the red-near infrared phosphors of examples 17-20 are shown in FIGS. 9 and 10. As is clear from fig. 9 and 10, the optimum amount of boric acid added was 2.5% of example 18.
Examples 21 to 25
Examples 21-25 provide red-near infrared phosphors having the formula: li (M) 1-x Cr x )O 2 Wherein M is Sc, x is 0.01, 0.02, 0.03, 0.04 and 0.05 respectively.
The red-near infrared phosphors of examples 21-25 were prepared in the same manner as in example 18.
The emission spectra and excitation spectra of the red-near infrared phosphors of examples 21-25 are shown in FIGS. 11 and 12. As can be seen from FIGS. 11 and 12, the red-near infrared phosphor which gives the best emission was Li (Sc) of example 22 0.98 Cr 0.02 )O 2
Examples 26 to 30
Examples 26-30 provide red-near infrared phosphors having the formula: li (Sc) 1-x-y Ga y )Cr x O 2 Wherein: x is 0.02, and y is 0, 0.2, 0.4, 0.6, 0.8, respectively.
The red-near infrared phosphors of examples 26 to 30 were prepared in the same manner as in example 22.
Emission spectra of the red-near infrared phosphors of examples 26 to 30,The excitation spectrum and XRD patterns are shown in FIGS. 13-15, respectively, due to the incorporation of Ga 3+ Cannot substitute Sc 3+ Occupying it in Li (Sc) 0.98 Cr 0.02 )O 2 Sites in the lattice, which are more prone to Li during temperature rise 2 CO 3 Formation of LiGaO 2 Thus doping Ga 3+ To Li (Sc) 0.98 Cr 0.02 )O 2 The lattice will cause a reduction in luminescence.
From examples 1 to 30, it is clear that Li (Sc) varies depending on the temperature rise, the holding time, the kind of flux and the amount of addition 1-x Cr x )O 2 The peak value of the emission wavelength of the fluorescent powder generates micro-movement, the movement range is 830nm-834nm, because the crystal field slightly changes due to different sintering environments, but the crystal field changes with Cr 3+ Increase in doping concentration x, Li (Sc) 1-x Cr x )O 2 The peak value of the emission wavelength of the fluorescent powder is obviously moved, and the peak value of the emission wavelength generates large movement within the range of 813-833nm when the Cr is 3+ When the concentration is reduced to x-0.02, the emission peak emits light most intensely at 820 nm. Emission wavelength and spectrum configuration with Cr 3+ The significant variation in concentration is due to the different concentrations of Cr 3+ Entering the crystal lattice changes the crystal field strength.
Example 31
Example 31 provides a red-near infrared phosphor having the formula:
Li[Sc 0.97 (Mg 0.005 Si 0.005 )]Cr 0.02 O 2
the emission spectrum and excitation spectrum of the red-near infrared phosphor of example 31 are shown in FIGS. 16 and 17.
Example 32
The present embodiment provides a red-near infrared LED device that uses Li (Sc) 0.98 Cr 0.02 )O 2 、(Ca,Sr)AlSiN 3 :Eu 2+ The mixture mixed with the transparent silica gel is defoamed, degassed, titrated on a blue light LED chip with the emission wavelength peak value of 450nm, and baked and cured to obtain the transparent silica gel;
the Li (Sc) 0.98 Cr 0.02 )O 2 Amount of (A) to be used、(Ca,Sr)AlSiN 3 :Eu 2+ The ratio of the dosage of (a) to the dosage of the transparent silica gel is 1.83: 0.05: 1.
the emission spectrum of the LED device and related parameters of the device in this embodiment are shown in fig. 18 and 19, and the device reaches the strongest emission at 843nm at 120mA driving current, at this time, the output power of the device is the maximum and can reach 18.25mW, and when the driving current is 20mA, the photoelectric conversion efficiency can reach 7.92% at the maximum.
Test example 1
This test example compares the red-near infrared LED device of this example 32 with the DNA synthesis rate and the absorption spectrum of cytochrome C oxidase, as shown in fig. 20:
the absorbance peaks of cytochrome C oxidase at 620, 820, 760 and 680nm were Cu A Reduced, oxidized, Cu B Reduced state, oxidized state. The infrared fluorescent powder can cover both (Cu) A Reduced, oxidized, Cu B Reduced state, oxidized state) at 820nm, theoretically, can accelerate electron transfer in the mitochondrial respiratory chain and can alleviate mitochondrial dysfunction in parkinson and alzheimer patients by increasing mitochondrial activity.
Because the genetic material of human cells is DNA, the infrared fluorescent powder and the emitted light can theoretically regulate the growth of various cells of the human body including neuron cells, microglia and the like by regulating and controlling the synthesis rate of the DNA.
Therefore, the red light-near infrared light fluorescent powder and the red light-near infrared light LED device have the potential of photobiotics for treating the neurological diseases. Since PBM has important applications in the treatment of neurodegenerative diseases represented by parkinson's disease and alzheimer's disease, more and more studies are actively advancing the work. Table 1 summarizes experimental models and wavelengths, light doses and efficacy of photobiotherapy for neurological disorders. The data in Table 1 show that near-red light with a peak wavelength of 800-.
TABLE 1
Figure BDA0003686691580000131
Test example 2
This test example utilized a red-near infrared LED device Li (Sc) 0.98 Cr 0.02 )O 2 Performing light-induced lactobacillus experiment, culturing lactobacillus in 37 deg.C constant temperature incubator in dark place for 24 hr by solid culture method, wherein the concentration of lactobacillus in the solid culture medium is controlled within a range of 30-300cfu/ml, and the lactobacillus in the culture medium receives 20mW/cm per day 2 The light dose and the irradiation density are 1.5J/cm 2 Irradiating in a pulse mode for 3 times a day, wherein each irradiation is 0.5J/cm 2 Colonies in each medium were counted or aligned 2h after the end of the last light exposure. FIGS. 21(a) - (b) are the culture medium after 24h incubation, (a) no light dark incubation, and (b) use of a red-near infrared LED device Li (Sc) 0.98 Cr 0.02 )O 2 In the culture medium subjected to PBM, the lactobacillus irradiated by 820nm can be obviously seen to grow in a sheet connection manner, and cannot be counted because the lactobacillus grows too fast and densely, but the growth promotion effect of the light source is macroscopically verified. The action mechanism of lactic acid bacteria in PD and AD is combined, and the red light-near infrared light LED device Li (Sc) provided by the invention 0.98 Cr 0.02 )O 2 And the emitted light can promote the growth of probiotics represented by lactic acid bacteria, so that the treatment of the neurological diseases is realized.
Having described embodiments of the present invention, the foregoing description is intended to be exemplary, not exhaustive, and not limited to the embodiments disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the described embodiments.

Claims (10)

1. A red light-near infrared light LED device is characterized in that the LED device is prepared by mixing red light-near infrared light fluorescent powder, transparent silica gel and optional red light fluorescent powder and packaging the mixture by a packaging process;
the chemical formula of the red light-near infrared light fluorescent powder is as follows: li (M) 1-x Cr x )O 2 Wherein M is at least one of Sc, Al, Ga, In, Lu, Be, Mg, Si and Ge, 0<x<0.10。
2. The red-near infrared LED device of claim 1, wherein the red-near infrared phosphor has a chemical formula of: li [ A ] 1-x-2z (B z C z )]Cr x O 2 Wherein A is at least one of Sc, Al, Ga, In and Lu, B is Be and/or Mg, C is Si and/or Ge, 0<x<0.10,0<z<0.01。
3. The red-near infrared LED device of claim 2,
the raw material containing the element M is at least one of oxide, nitrate, oxalate and carbonate containing the element M;
the raw material containing the element A is at least one of oxide, nitrate, oxalate and carbonate containing the element A;
the raw material containing the element B is at least one of oxide, nitrate, oxalate and carbonate containing the element B;
the raw material containing the element C is at least one of oxide, nitrate, oxalate and carbonate containing the element C.
4. The red-near infrared LED device of claim 1, wherein the red-near infrared phosphor has a chemical formula of: li (Sc) 1-x-y Ga y )Cr x O 2 Wherein 0 is<y<1。
5. The red-near infrared LED device of claim 1, wherein the red-near infrared phosphor has a chemical formula of: li (Sc) 1-x-m Al m )Cr x O 2 Wherein 0 is<m<1。
6. The red-near infrared LED device according to claim 1, wherein the method for preparing the red-near infrared phosphor comprises:
the first step is as follows: will contain Cr 3+ Grinding and mixing the raw material containing the element M and the fluxing agent uniformly, and carrying out primary calcination to obtain a product in the first step;
the second step is that: and grinding the product obtained in the first step, then carrying out secondary calcination, crushing, grinding, washing, filtering and drying to obtain the red light-near infrared light fluorescent powder.
7. The red-near infrared LED device of claim 6,
the operating conditions of the first calcination include: heating to 300 ℃ at a speed of 3-10 ℃/min in air, preserving heat for 0.3-2 hours, heating to 1000 ℃ at a speed of 3-10 ℃/min, preserving heat for 1-3 hours, cooling to 350 ℃ at a speed of 250 ℃ at a speed of 5-10 ℃/min, powering off, and cooling to 25-30 ℃ along with the furnace;
the operating conditions of the second calcination include: heating to 900 ℃ at a speed of 3-10 ℃/min in the air, preserving heat for 0.5-1.5 hours, heating to 1100-;
the addition amount of the fluxing agent is 1.5-3.5% of the total mass of the raw materials used for preparing the red light-near infrared light fluorescent powder;
the fluxing agent is at least one of aluminum fluoride, barium fluoride, ammonium chloride, ammonium fluoride, ammonium bifluoride and boric acid, and preferably the fluxing agent is boric acid.
8. The red-near infrared LED device of claim 1,
the ratio of the dosage of the red light-near infrared light fluorescent powder to the dosage of the red light fluorescent powder to the dosage of the transparent silica gel is (1-3) to (0-0.1) to 1;
the chemical formula of the red phosphor is (Ca, Sr) AlSiN 3 :Eu 2+ Or is orIs Q 2 Si 5 N 8 :Eu 2+ Wherein Q is at least one of Sr, Ca, Ba and Mg;
the packaging process comprises the following steps: defoaming and degassing a mixture of red light-near infrared light fluorescent powder, transparent silica gel and optional red light fluorescent powder, then titrating the mixture on a blue light LED chip, and baking and curing the mixture to obtain the red light-near infrared light LED device;
preferably, the peak value of the emission wavelength of the blue LED chip is 400-500 nm.
9. The red-near infrared LED device according to any of claims 1 to 8, wherein the emission wavelength range of the red-near infrared LED device is 700-950nm, and the emission wavelength peak is 813-835 nm.
10. Use of a red-near infrared LED device according to any one of claims 1-9 as a light source for the treatment of gastrointestinal, neurological and juvenile myopia.
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