Manufacturing method of Mn-doped water-soluble group IIB-VIA nano particles
A nanoparticle, water-soluble technology, applied in the field of preparation of water-soluble IIB-VIA group nanoparticles, can solve problems such as restricted use
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Embodiment 1
[0017] Embodiment 1 ZnS: the preparation of Mn
[0018] 863.9mg of Zn(ClO 4 ) 2 ·6H 2 O, 62.8mg of Mn(CH 3 COO) 2 ·6H 2 O and 678.8 mg of mercaptopropylene glycol were dissolved in 200 ml of water, and the pH value of the above-mentioned mixed solution was adjusted to 8.2 with 0.5 M NaOH solution; then deoxygenated with nitrogen bubbles; after 30 minutes, 293.3 mg of NaOH 2 S·9H 2 5ml of deoxygenated aqueous solution of O was added to the solution, under the protection of nitrogen, reflux reaction for 20 hours, and then cooled to room temperature; the pH value of the solution was adjusted to 7-8 with 0.2M hydrochloric acid, then evaporated and concentrated to 30ml-50ml, and then The solution is adjusted to pH=4.5 with hydrochloric acid, and acetone is added to produce a white precipitate; after centrifugal separation and vacuum drying, a white product nanoparticle ZnS:Mn is obtained, and the luminous efficiency can reach 40%.
Embodiment 2
[0019] Embodiment 2 ZnS: the preparation of Mn
[0020] 766mg of Zn(ClO 4 ) 2 ·6H 2 O, 126mg of Mn(CH 3 COO) 2 ·6H 2 O and 669 mg of mercaptopropylene glycol were dissolved in 200 ml of water, and the pH of the above-mentioned mixed solution was adjusted to be 7.5 with 0.5 M NaOH solution, and then deoxygenated with nitrogen bubbles; after 30 minutes, 291 mg of NaOH 2 S·9H 2 Add 5ml of deoxygenated aqueous solution of O into the solution, under the protection of nitrogen, reflux for 18 hours, then cool to room temperature; use 0.2M hydrochloric acid to adjust the pH value of the solution to between 7-8, and then evaporate and concentrate to 30ml-50ml , and then adjust the solution to pH=4.0 with hydrochloric acid, and add ethanol to make it produce white precipitate; after centrifugation and vacuum drying, a white product nanoparticle ZnS:Mn is given, and the luminous efficiency can reach 20%.
Embodiment 3
[0021] Example 3 Preparation of ZnS:Mn
[0022] 950mg of Zn(ClO 4 ) 2 ·6H 2 O, 32.9 mg of Mn(CH 3 COO) 2 ·6H 2 O and 670 mg of mercaptopropylene glycol were dissolved in 200 ml of water, and the pH of the above-mentioned mixed solution was adjusted to 8.2 with 0.5 M NaOH solution; then deoxygenated with nitrogen bubbles; after 30 minutes, 290 mg of NaOH 2 S·9H 2Add 5ml of deoxygenated aqueous solution of O into the solution, under the protection of nitrogen, reflux for 18 hours; then cool to room temperature, adjust the pH value of the solution to 7-8 with 0.2M hydrochloric acid, and then evaporate and concentrate to 30ml-50ml , and then use hydrochloric acid to adjust the solution to about pH=4.5, add acetone to make it produce white precipitate; after centrifugal separation and vacuum drying, a white product nanoparticle ZnS:Mn is given, and the luminous efficiency can reach 31%.
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