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Room-temperature phosphorescent material as well as preparation method and application thereof

A room temperature phosphorescence and hydrothermal reaction technology, applied in the field of room temperature phosphorescence materials and their preparation, can solve the problems of poor water dispersibility, biological toxicity and high cost

Active Publication Date: 2021-08-10
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, organometallic complexes usually contain noble metals, which are costly and potentially biotoxic (J.Am.Chem.Soc.2015,137,5304; J.Am.Chem.Soc.2013,135,14125.); another On the one hand, pure organic compounds usually need to introduce specific matrix and crystal structure, resulting in poor water dispersibility (Nat.Mater.2015,14,685; Sci.Adv.2018,4:eaas9732.)

Method used

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  • Room-temperature phosphorescent material as well as preparation method and application thereof
  • Room-temperature phosphorescent material as well as preparation method and application thereof
  • Room-temperature phosphorescent material as well as preparation method and application thereof

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preparation example Construction

[0043] A method for preparing a room temperature phosphorescent material, comprising the steps of:

[0044] S1. Dispersing the organosilane and the reducing agent in water to obtain a dispersion;

[0045] S2. Dispersing the zinc source in the dispersion liquid to obtain a reaction precursor solution;

[0046] S3, subjecting the reaction precursor solution to a hydrothermal reaction;

[0047] S4. Separating the solid product of the hydrothermal reaction to obtain a room temperature phosphorescent material.

[0048] Among them, the organosilane is the precursor of the silicon oxide framework, and the purpose of the zinc source is to provide zinc ions. Preferably, the organosilane is selected from (3-aminopropyl) trimethoxysilane or (3-aminopropyl) triethoxysilane; the reducing agent is selected from trisodium citrate or citric acid; the The zinc source is selected from one or more of zinc nitrate, zinc chloride, or zinc sulfate.

[0049] In step S1, preferably, the step of d...

Embodiment 1

[0067] Mix and disperse 4g (3-aminopropyl)trimethoxysilane and 0.3g trisodium citrate in 30mL deionized water, keep stirring for more than 15min, and pass through nitrogen protection to obtain a dispersion. 0.00025 mol of zinc nitrate was added to the dispersion and stirred overnight to obtain a reaction precursor solution. The reaction precursor solution was transferred to a reaction kettle, and put into an oven for hydrothermal reaction; the reaction conditions were heating time of 10 hours and heating temperature of 220°C. After the reaction is completed, cool to room temperature and perform centrifugation washing at 8000 rpm for 5 minutes each time, repeating 4 times, and the obtained lower layer precipitate is the room temperature phosphorescent material.

Embodiment 2

[0069] Mix and disperse 4g (3-aminopropyl)trimethoxysilane and 0.3g trisodium citrate in 30mL deionized water, keep stirring for more than 15min, and pass through nitrogen protection to obtain a dispersion. 0.0005 mol of zinc nitrate was added to the dispersion and stirred overnight to obtain a reaction precursor solution. The reaction precursor solution was transferred to a reaction kettle, and put into an oven for hydrothermal reaction; the reaction conditions were heating time of 10 hours and heating temperature of 220°C. After the reaction is completed, cool to room temperature and perform centrifugation washing at 8000 rpm for 5 minutes each time, repeating 4 times, and the obtained lower layer precipitate is the room temperature phosphorescent material.

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Abstract

The invention discloses a room-temperature phosphorescent material, the room-temperature phosphorescent material is nano spherical powder, and the nano spherical powder comprises a silicon oxide skeleton and zinc ions doped in the silicon oxide skeleton. The room-temperature phosphorescent material does not contain noble metal, so that potential biotoxicity introduced by the noble metal is avoided. According to the room-temperature phosphorescent material, the phosphorescent lifetime is about 236 milliseconds, and the fluorescent lifetime is about 13 nanoseconds; blue fluorescence can be emitted under the excitation of ultraviolet light, and a green room-temperature phosphorescence signal of about 8 seconds can be observed by naked eyes after an ultraviolet lamp is turned off. The room-temperature phosphorescent material has good water dispersibility and excellent pH and light stability (stable fluorescence and phosphorescent emission can be maintained under ultraviolet irradiation for 200 minutes). The room-temperature phosphorescent material can also be used as a phosphorescent probe with a high signal-to-noise ratio by utilizing unique optical characteristics, and is used for background-free biological imaging. The invention also provides a preparation method and application of the room-temperature phosphorescent material.

Description

technical field [0001] The invention belongs to the technical field of phosphorescent materials, and relates to a room temperature phosphorescent material and its preparation method and application. Background technique [0002] Due to its long emission lifetime (milliseconds to seconds), large Stokes shift and rich excited state energy level structure, room temperature phosphorescent materials have high application value in the fields of optoelectronic device preparation, chemical sensing and biological imaging. [0003] Currently, room-temperature phosphorescent materials based on organometallic complexes and pure organic compounds have been extensively studied. However, organometallic complexes usually contain noble metals, which are costly and potentially biotoxic (J.Am.Chem.Soc.2015,137,5304; J.Am.Chem.Soc.2013,135,14125.); another On the other hand, pure organic compounds usually need to introduce specific matrix and crystal structure, resulting in poor water dispersi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C09K11/59B82Y20/00B82Y40/00G01N21/64
CPCC09K11/595B82Y20/00B82Y40/00G01N21/64G01N21/6408
Inventor 何耀宋斌崔明月
Owner SUZHOU UNIV