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A kind of self-activated vanadate fluorescent powder and its preparation method and application

A type of vanadate and phosphor technology, which is applied in the field of self-activating vanadate phosphor and its preparation, can solve the problems of low photoelectric conversion efficiency and the like, and achieve the effects of high repeatability and simple synthesis method.

Inactive Publication Date: 2017-03-29
NORTHWEST UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

At present, light-converting LEDs are a research hotspot, and phosphor materials in light-converting LEDs are essential; and the problem faced by solar cells is that the photoelectric conversion efficiency is low, and the solar energy can be effectively improved by adding a light conversion layer on its surface. Photoelectric conversion efficiency of the battery

Method used

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  • A kind of self-activated vanadate fluorescent powder and its preparation method and application
  • A kind of self-activated vanadate fluorescent powder and its preparation method and application
  • A kind of self-activated vanadate fluorescent powder and its preparation method and application

Examples

Experimental program
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Effect test

Embodiment 1

[0032] This embodiment prepares self-activated vanadate Na by sol-gel method 2 YMg 2 V 3 o 12 The sample preparation process is as follows:

[0033] 1) According to the reactant cation molar ratio Na + :Y 3+ :Mg 2+ = 2:1:2 Weigh the raw material Na respectively 2 CO3 (AR)0.2120g, Y(NO 3 ) 3 ·6H 2 O0.7660g, Mg(NO 3 ) 2 ·6H 2 O(AR) 1.0256g, add distilled water and stir to obtain solution A;

[0034] Weigh citric acid 4.2028g and NH 4 VO 3 (AR) 0.7019g, slowly add solution A, stir while adding, until complete reaction, obtain uniform solution A;

[0035] 2) Put the solution into an oven and keep it warm at 60°C for 72 hours to form a uniform transparent colloid, then raise the temperature to 120°C and keep it warm for 12 hours to obtain a brown precursor;

[0036] 3) Fully grind the precursor, pre-calcine at 500°C for 4 hours to obtain a fluffy gray starting material, fully grind the starting material and calcinate at 700°C for 5 hours, cool and grind to obtain a ...

Embodiment 2

[0039] This embodiment prepares self-activated vanadate Na by sol-gel method 2 Y 0.95 Eu 0.05 Mg 2 V 3 o 12 The sample preparation process is as follows:

[0040] 1) According to the reactant cation molar ratio Na + :Y 3+ :Mg 2+ =2:0.95:2 Weigh the raw material Na respectively 2 CO 3 (AR)0.2120g, Y(NO 3 ) 3 ·6H 2 O0.7277g, Mg(NO 3 ) 2 ·6H 2 O(AR) 1.0256g, measure 0.02mol / L of Eu(NO 3 ) 3 Solution 5mL was mixed and stirred to obtain solution A;

[0041] Weigh citric acid 4.2028g and NH 4 VO 3 (AR) 0.7019g, slowly add solution A, stir while adding, until complete reaction, obtain uniform solution B;

[0042] 2) Put solution B in an oven and keep it warm at 70°C for 48 hours to form a uniform transparent colloid, then raise the temperature to 110°C and keep it warm for 36 hours to obtain a brown precursor;

[0043] 3) Fully grind the precursor, pre-calcine at 500°C for 5 hours to obtain a fluffy gray starting material, fully grind the starting material, calci...

Embodiment 3

[0046] This embodiment prepares self-activated vanadate Na by sol-gel method 2 Y 0.9 Eu 0.1 Mg 2 V 3 o 12 The sample preparation process is as follows:

[0047] 1) According to the reactant cation molar ratio Na + :Y 3+ :Mg 2+ =2:0.9:2 Weigh the raw material Na respectively 2 CO 3 (AR)0.2120g, Y(NO 3 ) 3 ·6H 2 O0.6894g, Mg(NO 3 ) 2 ·6H 2 O(AR) 1.0256g, measure 0.02mol / L of Eu(NO 3 ) 3 Solution 10mL was mixed and stirred to obtain solution A;

[0048] Weigh citric acid 4.2028g and NH 4 VO 3 (AR) 0.7019g, slowly add solution A, stir while adding, until complete reaction, obtain uniform solution B;

[0049] 2) Put solution B in an oven and keep it warm at 70°C for 48 hours to form a uniform transparent colloid, then raise the temperature to 110°C and keep it warm for 36 hours to obtain a brown precursor;

[0050] 3) Fully grind the precursor, pre-calcine at 500°C for 5 hours to obtain a fluffy gray starting material, fully grind the starting material, calcina...

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Abstract

The invention provides a self-activated vanadate fluorescent powder, a preparation method and application thereof. The general chemical formula of the self-activating vanadate phosphor is A2BMg2V3O12, wherein A is one of Li, Na, and K elements; B is one of Y, Gd, Bi, La, and Lu elements. The self-activated vanadate phosphor is synthesized by a sol-gel method, and the obtained sample can be excited by ultraviolet light of 200-400nm, and has broad-spectrum emission in the range of 350-700nm, with a main peak at 500nm. The self-activated vanadate phosphor can adjust its luminescence by doping Eu3+, Sm3+, Yb3+, Pr3+, Nd3+ and other rare earth ions, so as to realize its application in LED and solar cells.

Description

technical field [0001] The invention belongs to the technical field of solid-state luminescence in physics, and specifically relates to a self-activated vanadate phosphor and a preparation method thereof, and also relates to the application of the phosphor in white light LEDs and improving the photoelectric conversion efficiency of silicon-based solar cells . Background technique [0002] With the increasingly severe energy crisis and environmental pollution, more and more attention has been paid to the development of new green energy production devices and environmentally friendly new lighting sources. As a new generation of energy-saving and efficient lighting sources, LEDs and solar cells with green production capacity are one of the important ways to solve this problem. At present, light-converting LEDs are a research hotspot, and phosphor materials in light-converting LEDs are essential; and the problem faced by solar cells is that the photoelectric conversion efficien...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C09K11/82C09K11/74H01L33/50H01L31/055
CPCY02E10/52
Inventor 郭崇峰宋丹
Owner NORTHWEST UNIV