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A kind of preparation method of rare earth doped zinc oxide

A technology of rare earth doping and zinc oxide, which is applied in the direction of zinc oxide/zinc hydroxide, nanotechnology, etc., to achieve the effects of good dispersion of rare earth elements, controllable morphology of rare earth/ZnO nanomaterials, and mild reaction conditions

Active Publication Date: 2020-09-29
SHAOXING UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The deep eutectic solvent has the advantages of simple preparation, strong solubility, good biocompatibility, and easy recycling. As a new type of green solvent, it has been used in the field of ZnO and other micro-nano materials. There are relatively few reports on solvents used as reaction substrates or starting materials to prepare micro-nanomaterials

Method used

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  • A kind of preparation method of rare earth doped zinc oxide
  • A kind of preparation method of rare earth doped zinc oxide
  • A kind of preparation method of rare earth doped zinc oxide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] (1) ZnCl 2 Stir and react with ChCl in a constant temperature oil bath at 100°C for 1 hour at a molar ratio of 2:1, and obtain uniform, colorless and transparent ZnCl after cooling 2 / ChCl deep eutectic solvent;

[0034] (2) adding in the deep eutectic solvent that step (1) makes is 0.5% Ce(NO 3 ) 3 ·6H 2 O was stirred until it was completely dissolved to obtain a light yellow mixed solution. Add distilled water with a volume ratio of 1:1 to the deep eutectic solvent, and then adjust the pH value of the solution to 8 with 25% ammonia water, and obtain a light yellow solution after ultrasonic mixing for 30 minutes. emulsion;

[0035] (3) Transfer the light yellow emulsion prepared in step (2) to a polytetrafluoro-lined hydrothermal synthesis reactor, then place the reactor in an oven at 120°C for 12 hours of hydrothermal reaction, after the reaction The reaction solution was cooled and centrifuged to obtain a light yellow solid, and the light yellow solid was washed...

Embodiment 2

[0039] (1) ZnBr 2 Stir and react with ChCl in a constant temperature oil bath at 100°C for 1 hour at a molar ratio of 2:1, and obtain uniform, colorless and transparent ZnCl after cooling 2 / ChCl deep eutectic solvent;

[0040] (2) adding in the deep eutectic solvent that step (1) makes is 1% Ce(CH 3 COO) 3 ·5H 2 O was stirred until it was completely dissolved to obtain a light yellow mixed solution. Add distilled water with a volume ratio of 2:1 to the deep eutectic solvent, and then adjust the pH value of the solution to 9 with 25% ammonia water, and obtain a light yellow solution after ultrasonic mixing for 30 minutes. emulsion;

[0041] (3) Transfer the light yellow emulsion prepared in step (2) to a PTFE-lined hydrothermal synthesis reactor, then place the reactor in an oven at 140°C for 11 hours of hydrothermal reaction, after the reaction The reaction solution was cooled and centrifuged to obtain a light yellow solid, which was alternately washed with ethanol and d...

Embodiment 3

[0045] (1) ZnCl 2 Stir and react with ChCl in a constant temperature oil bath at 100°C for 1 hour at a molar ratio of 2:1, and obtain uniform, colorless and transparent ZnCl after cooling 2 / ChCl deep eutectic solvent;

[0046] (2) adding in the deep eutectic solvent that step (1) makes is 2% Ce(NO 3 ) 3 ·6H 2 O was stirred until it was completely dissolved to obtain a light yellow mixed solution. Add distilled water with a volume ratio of 2:1 to the deep eutectic solvent, and then adjust the pH value of the solution to 10 with 25% ammonia water, and obtain a light yellow solution after ultrasonic mixing for 30 minutes. emulsion;

[0047] (3) Transfer the light yellow emulsion prepared in step (2) to a PTFE-lined hydrothermal synthesis reactor, then place the reactor in an oven at 160°C for 10 hours of hydrothermal reaction, after the reaction The reaction solution was cooled and centrifuged to obtain a light yellow solid, and the light yellow solid was washed alternately...

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Abstract

The invention discloses a preparation method of rare earth doped zinc oxide, which comprises the following steps: (1) adding ZnCl 2 or ZnBr 2 Prepare ZnCl with ChCl at a molar ratio of 2:1 2 / ChCl or ZnBr 2 / ChCl deep eutectic solvent; (2) adding in the deep eutectic solvent is 0.5~2% Ce(CH 3 COO) 3 ·5H 2 O or Ce(NO 3 ) 3 ·6H 2 O, adjust the pH value to 8-10 with ammonia water to obtain a light yellow emulsion; (3) transfer the light yellow emulsion to a reaction kettle, put it in an oven for hydrothermal reaction at 120-160°C, and obtain a light yellow powder solid; (4) the pale yellow powdery solid is calcined in an air atmosphere of 450-550° C. in a tube furnace to obtain Ce / ZnO nanomaterials. The invention has the advantages of mild reaction conditions, good dispersion of rare earth elements, controllable morphology of rare earth / ZnO nanometer materials, and the like.

Description

technical field [0001] The invention relates to the technical field of preparation of functional materials, in particular to a kind of ZnCl 2 / ChCl or ZnBr 2 The / ChCl deep eutectic solvent is simultaneously a zinc source and a solvent to prepare a method for rare earth cerium-doped zinc oxide. Background technique [0002] Zinc oxide (ZnO) is a II-VI group direct bandgap n-type semiconductor material. Under the irradiation of ultraviolet light with a wavelength below 387nm, it can be excited to generate photogenerated electron-hole pairs to generate hydroxyl radicals ( OH) and Superoxide radical (·O 2 – ) and other active free radicals with strong oxidizing ability are used for photocatalytic degradation of pollutants such as organic dyes. However, due to the limitation of the forbidden band width, ZnO can only absorb a very small amount of ultraviolet light in sunlight, resulting in a low utilization rate of solar energy; at the same time, the photogenerated electron-h...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G9/02B82Y40/00
CPCB82Y40/00C01G9/02C01P2002/54C01P2002/72C01P2004/03C01P2004/04C01P2004/32C01P2004/64
Inventor 许映杰
Owner SHAOXING UNIVERSITY