GREEN LUMINESCENT MATERIAL OF TERBIUM DOPED GADOLINIUM BORATE AND PREPARing METHOD THEREOF

Abstract

A green luminescent material of terbium doped gadolinium borate is provided. The luminescent material has a formula of M3Gd1-xTbx(BO3)3, wherein, M is alkaline earth metal element and x is 0.005-0.5. The method for preparing the luminescent material comprises the following steps: selecting the source compounds of alkaline earth metal ion, boric acid radical ion (BO33−), Gd3+ and Tb3+ by the stoichiometric ratio, wherein, the stoichiometric ratio is the molar ratio of the corresponding element in the formula of M3Gd1-xTbx(BO3)3, and the source compound of BO33 is over 10%-30% by the molar ratio; mixing; pre-treatment by sintering; cooling; grinding; calcination; and cooling to obtain the luminescent material.

Description

FIELD OF THE INVENTION

The present disclosure relates to luminescent materials, especially to a green luminescent material of terbium doped gadolinium borate which excited by vacuum ultraviolet light and a preparing method thereof.

BACKGROUND OF THE INVENTION

Compared to the CRT display and the LCD display, the plasma panel display (PDP) has a lot of outstanding features, such as, broad angular field of view, large areas, high speed of response, and colors non-distortion. The PDP can be used to produce large size displays, which is optimal to wall type TVs. Without mercury that is poisonous to human, mercury-free fluorescence lamps have significant meanings to environment protection in comparison with the common high-voltage mercury lamps and low-voltage mercury lamps. In a PDP display, the circuit and luminescent material therein may be key techniques for displaying. Selecting luminescent material is the most important techniques in displays. Accordingly, study of tricolor fluorescence powders used as luminescent materials in the PDP is essential. Recently, the most widely used tricolor fluorescence powders include red powders such as Y₂O₃:Eu³⁺ and (Y,Gd)BO₃:Eu³⁺, green powders such as Zn₂SiO₄:Mn²⁺ and BaAl₁₂O₁₉:Mn²⁺, and blue powders such as BaMgAl₁₀O₁₇:Eu²⁺. For the commercial green powder Zn₂SiO₄:Mn²⁺, a spin forbidden (⁴T₁→⁶A₁) emission of the Mn²⁺ therein resulting in prolonging the afterglow time of the material, which is not beneficial to the display of rapidly moving images of TVs and is not suitable for TV displays. An increasing of doping concentration of the Mn²⁺ can shorten the afterglow time, however, the luminescence intensity of the material is reduced. So, it is necessary to develop a new, efficient green luminescent material with short afterglow time Now the studies of luminescent material of gadolinium borate M₃Gd(BO₃)₃ (M=Ca, Sr, Ba) mainly focus on its laser characteristics when being doped in rare earth elements as a mono-crystal. In contrast, the researches of that in excitation under vacuum ultraviolet light are less. Compared to the long afterglow of the Mn²⁺, the Tb³⁺ has a characteristic emission of green light (540-545 nm), and the spin coupling of the Tb³⁺ has a shielding affect to the spin forbidden of the Tb³⁺, which endows it with shorter afterglow time and overcomes hysteresis effect.

Accordingly, to overcome the disadvantage of long afterglow time, and to meet the requirement of color displaying and green illumination, a new green luminescent material which has a short afterglow time should be developed and be applied in plasma panel display (PDP) or mercury-free fluorescence lamps.

SUMMARY OF THE INVENTION

The technical problem of the present invention to be solved is to provide a green luminescent material of terbium doped gadolinium borate which has high luminescence intensity, and a preparing method for preparing the green luminescent material of terbium doped gadolinium borate.

The technical solution to solve the technical problem in the present invention is: providing a green luminescent material of terbium doped gadolinium borate, the green luminescent material of terbium doped gadolinium borate has a chemical formula of M₃Gd_1-xTb_x(BO₃)₃, wherein, M is alkaline earth metal element, and x is 0.005-0.5. The said alkaline earth metal element M is at least one of calcium (Ca), strontium (Sr), and barium (Ba).

And, a preparing method for preparing the green luminescent material of terbium doped gadolinium borate comprises the following steps:

Step one, selecting the source compounds of alkaline earth metal ion, the source compounds of boric acid radical ion (BO₃²⁻), the source compounds of Gd³⁺, and the source compounds of Tb³⁺ by the stoichiometric ratio, wherein, the stoichiometric ratio is the molar ratio of the corresponding element in the formula of M₃Gd_1-xTb_x(BO₃)₃, and the source compound of BO₃²⁻ is over 10%-30% by the molar ratio; M is alkaline earth metal element, and x is 0.005-0.5;

Step two, mixing each compound;

Step three, pre-treating the mixture by sintering and then cooling the mixture;

Step four, grinding the sintered matter, calcining the grinded matter in reducing atmosphere and then cooling to get the green luminescent material of terbium doped gadolinium borate.

In the preparing method of the present invention, the source compound of the alkaline earth metal element is at least one of alkaline earth oxide, alkaline earth hydroxide, alkaline earth nitrate, and alkaline earth carbonate. The source compound of the boric acid radical ion is at least one of boric acid and boric oxide. The source compound of Gd³⁺ is Gd³⁺ contained rare earth oxide or Gd³⁺ contained nitrate. The source compound of Tb³⁺ is Tb³⁺ contained rare earth oxide or Tb³⁺ contained nitrate.

In the preparing method of the present invention, the compounds are mixed with fluxing agents.

In the preparing method of the present invention, the fluxing agent is at least one of the boric acid and barium fluoride.

In the preparing method of the present invention, pre-treatment by sintering is carried out at the temperature in a range of 200-700° C. for 2 hours to 7 hours.

In the preparing method of the present invention, calcining the grinded matter is carried out at the temperature in a range of 900-1100 ° C. for 3 hours to 24 hours.

In the preparing method of the present invention, the source compound of boric acid radical ion is over 10%-20% by the molar ratio.

In the preparing method of the present invention, the reducing atmosphere is gas mixture of N₂ and H₂, H₂, or carbon monoxide.

The luminescent material of the present invention has a matrix of M₃Gd_1-xTb_x(BO₃)₃. The M₃Gd_1-xTb_x(BO₃)₃ has a strong absorption of the 150 nm-175 nm vacuum ultraviolet light (VUV), and transits the energy to the Gd ions. There is an energy transition between the Gd³⁺⁶P_J energy levels and the Tb³⁺, after the energy absorption of Tb³⁺, it emits green photons by f-f transition radiation. The energy transition process between the Gd³⁺⁶P_J energy levels and the Tb³⁺ enhances the green light emission intensity of the Tb³⁺. Compared to the existing technology, the luminescent materials of the present invention have the following advantages: 1. Gd³⁺ contained in the gadolinium borate M₃Gd(BO₃)₃ (M=Ca, Sr, Ba) is a framework structure of the M₃Gd(BO₃)₃, there is energy transition between the Gd³⁺ and the Tb³⁺, which can improve the green light emission intensity of the Tb³⁺; 2. compared to the long afterglow time of Mn²⁺, the Tb³⁺ has characteristic green light emission (540-545 nm), and the spin coupling of the Tb³⁺ has a shielding affect to the spin forbidden of the Tb³⁺, which endows it with shorter afterglow time and overcomes hysteresis effect.

In the preparing method for preparing the green luminescent material of terbium doped gadolinium borate, by sintering treatment and calcining treatment, the luminescent materials can be obtained, which makes the process simple, low cost, and have broad producing and applying prospect.

BRIEF DESCRIPTION OF THE DRAWINGS

Further description of the present invention will be illustrated, which combined with drawings and embodiments in the drawings.

FIG. 1 shows an excitation spectrum of the luminescent material of Sr₃Gd_0.85Tb_0.15(BO₃)₃ of example 1, the excitation spectrum is tested under a monitoring wavelength of 543 nm;

FIG. 2 shows emission spectrums of the luminescent material of Sr₃Gd_0.85Tb_0.15(BO₃)₃ of example 1 and a commercial BaAl₁₂O₁₉:Mn²⁺, the emission spectrums are tested under an excitation wavelength of 172 nm;

FIG. 3 shows emission spectrums of the luminescent material of Sr₃Gd_0.85Tb_0.15(BO₃)₃ of example 1 and the luminescent material of Sr₃Y_0.85Tb_0.15(BO₃)₃ of comparison example 1, the emission spectrums are tested under an excitation wavelength of 172 nm;

FIG. 4 shows a flow chat for preparing the green luminescent material of terbium doped gadolinium borate.

DETAILED DESCRIPTION OF ILLUSTRATED EMBODIMENTS

The examples hereinafter described merely being preferred or exemplary embodiment of the disclosure. It will be apparent that various changes may be made thereto without departing from the spirit and scope of the disclosure.

According to an embodiment of a green luminescent material of terbium doped gadolinium borate, the green luminescent material of terbium doped gadolinium borate has a chemical formula of M₃Gd_1-xTb_x(BO₃)₃, wherein, M is alkaline earth metal element, and x is 0.005-0.5.

The green luminescent material of terbium doped gadolinium borate taking M₃Gd(BO₃)₃ as the matrix and doped luminescent ion Tb²⁺, where the mechanism is: Through the strong absorption of the 150 nm-175 nm vacuum ultraviolet light (VUV), energy is transmitted to the Gd ions. There is an energy transition between the Gd³⁺⁶P_J energy levels and the Tb³⁺, after the energy absorption of Tb³⁺, it emits green photons by f-f transition radiation. The energy transition process between the Gd³⁺⁶P_J energy levels and the Tb³⁺ enhances the green light emission intensity of the Tb³⁺.

Referring to FIG. 1, the strong absorption peak at the vacuum ultraviolet wave band of 150-200 nm is an absorption peak of the matrix. The luminescent material of example 1 has a strong absorption at the vacuum ultraviolet wave band, which can effectively transit the energy to the Gd³⁺, achieve an energy transition between Gd—Tb, and enhance the characteristic emission intensity of the Tb³⁺ at 543 nm.

Referring to FIG. 2, the curve 1 shows an emission spectrum of Sr₃Gd_0.85Tb_0.15(BO₃)₃ under an excitation wavelength of 172 nm, the curve 2 shows an emission spectrum of commercial green powder BaAl₁₂O₁₉:Mn²⁺ under an excitation wavelength of 172 nm. Obviously, the intensity of the emission peak of the Sr₃Gd_0.85Tb_0.15(BO₃)₃ at 543 nm is greater than the intensity of the emission peak of the commercial green powder BaAl₁₂O₁₉:Mn²⁺ at 525 nm. The intensity of the emission peak of the Sr₃Gd_0.85Tb_0.15(BO₃)₃ of example 1 at 543 nm is 1.8 times to that of the commercial powder BaAl₁₂O₁₉:Mn²⁺. The luminescent material of example 1 has a high effect, and a short afterglow time, which overcomes hysteresis effect. The Tb³⁺ doped in the green luminescent material of gadolinium borate at least has the following advantages : (1) Gd³⁺ contained in the gadolinium borate M₃Gd(BO₃)₃ (M=Ca, Sr, Ba) is a framework structure of the M₃Gd(BO₃)₃, there is energy transition between the Gd³⁺—Tb³⁺, which can improve the green light emission intensity of the Tb³⁺; (2) compared to the long afterglow time of Mn²⁺, the Tb³⁺ has characteristic green light emission (540-545 nm), and the spin coupling of the Tb³⁺ has a shielding affect to the spin forbidden of the Tb³⁺, which endows it with shorter afterglow time and overcomes hysteresis effect.

Referring to FIG. 4, a flow chart of a preparing method for preparing the green luminescent material of terbium doped gadolinium borate includes the following steps:

S01, selecting the source compounds of alkaline earth metal ion, the source compounds of boric acid radical ion (BO₃²⁻), the source compounds of Gd³⁺, and the source compounds of Tb³⁺ by the stoichiometric ratio, wherein, the stoichiometric ratio is the molar ratio of the corresponding element in the formula of M₃Gd_1-xTb_x(BO₃)₃, and the source compound of BO₃²⁻ is over 10%-30% by the molar ratio, preferably, the source compound of BO₃²⁻ is over 10%-20% by the molar ratio, M is alkaline earth metal element, the alkaline earth metal element M is at least one of the Ca, Sr, and Ba, and x is 0.005-0.5;

S02, mixing each compound;

S03, pre-treating the mixture by sintering and then cooling the mixture;

S04, grinding the sintered matter, calcining the grinded matter in reducing atmosphere and then cooling to get the green luminescent material of terbium doped gadolinium borate.

In the step of S01, the source compound of the alkaline earth metal element is at least one of alkaline earth oxide, alkaline earth hydroxide, alkaline earth nitrate, and alkaline earth carbonate. The source compound of the boric acid radical ion is at least one of boric acid and boric oxide. The source compound of Gd³⁺ is Gd³⁺ contained rare earth oxide or Gd³⁺ contained nitrate. The source compound of Tb³⁺ is Tb³⁺ contained rare earth oxide or Tb³⁺ contained nitrate.

In the step of S02, the compounds are even mixed with a little fluxing agent, the fluxing agent is one or two elements selected from the group consisting of boric acid and barium fluoride.

In the step of S03, pre-treatment by sintering is carried out at the temperature in a range of 200- 700° C. for 2 hours to 7 hours, and then cooled to room temperature.

In the step of S04, calcining the grinded matter is carried out at the temperature in a range of 900-1100° C. for 3 hours to 24 hours in a box type high temperature furnace, and then cooled to room temperature. The reducing atmosphere is gas mixture of N₂ and H₂, H₂, or carbon monoxide.

Special examples are disclosed as follows to demonstrate the green luminescent material of terbium doped gadolinium borate and preparing method thereof.

EXAMPLE 1

2.2145 gram (g) strontium carbonate (SrCO₃), 0.7703 g gadolinium oxide (Gd₂O₃), 1.0666 g boric acid (H₃BO₃) (calculated by over 15% of the molar equivalence of the boron element contained in the products. The follows have the same calculation), 0.1402 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (weigh by 5% of the molar ratio to the products, the follows are the same) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 500° C. for 2 hours (h), and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1000° C. for 5 h in gas mixture of N₂ and H₂ (H₂ takes 5%), cooling, removing to be grinded to obtain green fluorescent luminescent material of Sr₃Gd_0.85Tb_0.15(BO₃)₃. In the present preparing method, barium fluoride acts as a fluxing agent, which cannot enter the crystal lattice, and do not affect the structure and compositions of the final product Sr₃Gd_0.85Tb_0.15(BO₃)₃ green fluorescent luminescent materials.

EXAMPLE 2

3.9201 g barium nitrate (Ba(NO₃)), 0.9017 g gadolinium oxide (Gd₂O₃), 1.2057 g boric acid (H₃BO₃) (over 15%), 0.0047 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 200° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 900° C. for 5 h in gas mixture of N₂ and H₂ (H₂ takes 5%), cooling, removing to be grinded to obtain green fluorescent luminescent material of Ba₃Gd_0.995Tb_0.005(BO₃)₃.

EXAMPLE 3

2.9600 g barium carbonate (BaCO₃), 2.1434 g gadolinium nitrate Gd(NO₃)₃·6H₂O, 1.0202 g boric acid (H₃BO₃) (over 10%), 0.0467 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 700° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1100° C. for 10 h in reducing gas of CO, cooling, removing to be grinded to obtain green fluorescent luminescent material of Ba₃Gd_0.95Tb_0.05(BO₃)₃.

EXAMPLE 4

1.1114 g calcium hydroxide (Ca(OH)₂), 0.6344 g gadolinium oxide (Gd₂O₃), 1.0202 g boric acid (H₃BO₃) (over 10%), and 0.2804 g terbium oxide (Tb₄O₇) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 600° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1000° C. for 24 h in reducing gas of CO, cooling, removing to be grinded to obtain green fluorescent luminescent material of Ca₃Gd_0.7Tb_0.3(BO₃)₃.

EXAMPLE 5

2.1407 g strontium carbonate (SrCO₃), 0.0370 g calcium hydroxide (Ca(OH)₂), 0.7703 g gadolinium oxide (Gd₂O₃), 1.0202 g boric acid (H₃BO₃) (over 10%), 0.1402 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 700° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1000° C. for 12 h in gas mixture of N₂ and H₂ (H₂ takes 5%), cooling, removing to be grinded to obtain green fluorescent luminescent material of Sr₃Ca_0.1Gd_0.85Tb_0.15(BO₃)₃.

EXAMPLE 6

2.0669 g strontium carbonate (SrCO₃), 0.0370 g calcium hydroxide (Ca(OH)₂), 0.0987 g barium carbonate (BaCO₃), 0.4531 g gadolinium oxide (Gd₂O₃), 1.0666 g boric acid (H₃BO₃) (over 15%), 0.4673 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 700° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1000° C. for 24 h in reducing gas of H₂, cooling, removing to be grinded to obtain green fluorescent luminescent material of Sr_2.8Ca_0.1Ba_0.1Gd_0.5Tb_0.5(BO₃)₃.

COMPARISON EXAMPLE 1

2.2145 g strontium carbonate (SrCO₃), 0.4795 g yttrium oxide (Y₂O₃), 1.0666 g boric acid (H₃BO₃) (over 15%), 0.1402 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 500° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1000° C. for 5 h in reducing gas mixture of N₂ and H₂ (H₂ takes 5%), cooling, removing to be grinded to obtain green fluorescent luminescent material of Sr₃Y_0.85Tb_0.15(BO₃)₃.

COMPARISON EXAMPLE 2

1.5013 g barium carbonate (BaCO₃), 0.7738 g lanthanum oxide (La₂O₃), 1.0202 g boric acid (H₃BO₃) (over 10%), 0.0467 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 500° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1100° C. for 5 h in reducing gas of CO, cooling, removing to be grinded to obtain green fluorescent luminescent material of Ba₃La_0.95Tb_0.05(BO₃)₃.

COMPARISON EXAMPLE 3

1.5013 g calcium carbonate (CaCO₃), 0.7250 g gadolinium oxide (Gd₂O₃), 0.0815 g lanthanum oxide (La₂O₃), 1.0202 g boric acid (H₃BO₃) (over 10%), 0.0934 g terbium oxide (Tb₄O₇), and 0.0438 g barium fluoride (BaF₂) (5%) are provided and completely grinded in an agate mortar. The grinded matter is pre-treated by sintering in a corundum crucible at 600° C. for 2 h, and then cooled to room temperature. The cooled sintered matter is completely grinded once more. Finally, calcining at 1000° C. for 10 h in reducing gas of CO, cooling, removing to be grinded to obtain green fluorescent luminescent material of Ca₃Gd_0.8La_0.1Tb_0.1(BO₃)₃.

Gd³⁺ contained in the gadolinium borate M₃Gd(BO₃)₃ (M=Ca, Sr, Ba) of examples 1-6 is a framework structure of the M₃Gd(BO₃)₃, there is energy transition between the Gd³⁺—Tb³⁺, which can improve the green light emission intensity of the Tb³⁺. While in the comparison examples 1-3, there is no energy transition between the Ln³⁺—Tb³⁺ of borate MLn(BO₃)₃ (M=Ca, Sr, Ba; Ln=La, Y etc.). Compared to the M₃Gd(BO₃)₃ (M=Ca, Sr, Ba), under the excitation of vacuum ultraviolet light, the MLn(BO₃)₃ (M=Ca, Sr, Ba; Ln=La, Y etc.) doped with Tb³⁺ has a lower luminescence intensity, shown in FIG. 3. The curve 3 shows an emission spectrum of the luminescent material of Sr₃Y_0.85Tb_0.15(BO₃)₃ under an excitation wavelength of 172 nm, the curve 4 shows an emission spectrum of the luminescent material of Sr₃Gd_0.85Tb_0.15(BO₃)₃ under an excitation wavelength of 172 nm.

In the green luminescent material of terbium doped gadolinium borate mentioned above, Through the strong absorption of the 150 nm-175 nm vacuum ultraviolet light (VUV) by matrix M₃Gd_1-xTb_x(BO₃)₃, energy is transmitted to the Gd ions. There is an energy transition between the Gd³⁺⁶P_J energy levels and the Tb³⁺, after the energy absorption of Tb³⁺, it emits green photons by f-f transition radiation. The energy transition process between the Gd³⁺⁶P_J energy levels and the Tb³⁺ enhances the green light emission intensity of the Tb³⁺.

Compared to the existing technology, the luminescent material of the present invention has the following advantages: 1. Gd³⁺ contained in the gadolinium borate M₃Gd(BO₃)₃ (M=Ca, Sr, Ba) is a framework structure of the M₃Gd(BO₃)₃, there is energy transition between the Gd³⁺—Tb³⁺, which can improve the green light emission intensity of the Tb³⁺; 2. compared to the long afterglow time OF Mn²⁺, the Tb³⁺ has characteristic green light emission (540-545 nm), and the spin coupling of the Tb³⁺ has a shielding affect to the spin forbidden of the Tb³⁺, which endows it with shorter afterglow time and overcomes hysteresis effect.

In the preparing method for preparing the green luminescent material of terbium doped gadolinium borate mentioned above, by pre-treatment by sintering and calcining treatment, the luminescent material can be obtained, which makes the preparation process simple, low cost, and have broad applying prospect.

It is believed that the exemplary embodiment and its advantages will be understood from the foregoing description, and it will be apparent that various changes may be made thereto without departing from the spirit and scope of the disclosure or sacrificing all of its advantages, the examples hereinbefore described merely being preferred or exemplary embodiment of the disclosure.

Claims

1. A green luminescent material of terbium doped gadolinium borate, which has a chemical formula of M3Gd1-xTbx(BO3)3, wherein, M is alkaline earth metal, and x is 0.005-0.5.

2. The green luminescent material of terbium doped gadolinium borate according to claim 1, wherein said alkaline earth metal M is selected from one or more ingredients of the group consisting of calcium, strontium, and barium.

3. A preparing method for making a green luminescent material of terbium doped gadolinium borate, comprising the following steps: step one, selecting the source compounds of alkaline earth metal ion, boric acid radical ion (BO32−), Gd3+, and Tb3+ by the stoichiometric ratio, wherein, the stoichiometric ratio is the molar ratio of the corresponding element in the formula of M3Gd1-xTbx(BO3)3, and the source compound of BO32− is over 10%-30% by the molar ratio, M is alkaline earth metal element, and x is 0.005-0.5;step two, mixing each compound;step three, pre-treating the mixture by sintering and then cooling the mixture;step four, grinding the sintered matter, calcining the grinded matter in reducing atmosphere and then cooling to get the green luminescent material of terbium doped gadolinium borate.

4. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 3, wherein the source compound of the alkaline earth metal element is at least one of alkaline earth oxide, alkaline earth hydroxide, alkaline earth nitrate, and alkaline earth carbonate; the source compound of the boric acid radical ion is at least one of boric acid and boric oxide; the source compound of Gd3+ is Gd3+ contained rare earth oxide or Gd3+ contained nitrate; the source compound of Tb3+ is Tb3+ contained rare earth oxide or Tb3+ contained nitrate.

5. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 3, wherein the compounds are even mixed with fluxing agents.

6. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 5, wherein the fluxing agent is selected from one or more elements of the group consisting of boric acid and barium fluoride.

7. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 3, wherein pre-treatment by sintering is carried out at the temperature in a range of 200-700° C. for 2 hours to 7 hours.

8. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 3, wherein calcining the grinded matter is carried out at the temperature in a range of 900-1100° C. for 3 hours to 24 hours.

9. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 3, wherein the source compound of BO32− is over 10%-20% by the molar ratio.

10. The preparing method for making a green luminescent material of terbium doped gadolinium borate according to claim 3, wherein the reducing atmosphere is gas mixture of N2 and H2, H2, or carbon monoxide.