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Direct synthesis method for preparing size-tunable lead chalcogenide quantum dots and its application

A synthesis method and quantum dot technology, applied in chemical instruments and methods, lead sulfide, semiconductor/solid-state device manufacturing, etc., can solve problems that hinder the progress of quantum dot devices

Active Publication Date: 2022-04-15
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The limitation of size adjustment also seriously hinders the progress of the industrialization of quantum dot devices.

Method used

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  • Direct synthesis method for preparing size-tunable lead chalcogenide quantum dots and its application
  • Direct synthesis method for preparing size-tunable lead chalcogenide quantum dots and its application
  • Direct synthesis method for preparing size-tunable lead chalcogenide quantum dots and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Preparation of PbS quantum dot ink

[0031] 1) Preparation of precursor solution: 2.766 g (6 mmol) of lead iodide, 228 mg (1 mmol) of N,N-diphenylthiourea, 4.5 mL of N,N-dimethylformamide and 4.5 mL of Add methyl sulfoxide into a 20mL single-necked flask, stir at room temperature until the precursor is completely dissolved, and obtain a precursor solution for use; wherein the volume ratio of N,N-dimethylformamide and dimethyl sulfoxide is 1 :1;

[0032] 2) Inject 1mL of butylamine into the one-necked flask, and continue stirring for 10 minutes. Transfer the reaction solution to a centrifuge tube, add toluene until the reaction solution becomes turbid, centrifuge at a speed of 8000 rpm, and discard the supernatant after centrifugation for 5 minutes; drain the obtained product under vacuum to synthesize PbS quantum dots Ink was stored in the glove box.

[0033] According to the technical solution of this embodiment, the mixed solvent of N,N-dimethylformamide and dimeth...

Embodiment 2

[0037] Preparation of PbS quantum dot ink

[0038]1) Preparation of precursor solution: 0.2766 g (0.6 mmol) of lead iodide, 22.8 mg (0.1 mmol) of N,N-diphenylthiourea, 4.5 mL of N,N-dimethylformamide and 4.5 mL of γ- Butyrolactone was added to a 20 mL single-necked flask, and stirred at room temperature until the precursor was completely dissolved to obtain a precursor solution for use; wherein the volume ratio of N,N-dimethylformamide and γ-butyrolactone was 1 :1;

[0039] 2) Inject 1mL of butylamine into the one-necked flask, and continue stirring for 10 minutes. Transfer the reaction solution to a centrifuge tube, add toluene until the reaction solution becomes turbid, centrifuge at a speed of 8000 rpm, and discard the supernatant after centrifugation for 5 minutes; drain the obtained product under vacuum to synthesize PbS quantum dots Ink was stored in the glove box.

[0040] According to the technical solution of this embodiment, the mixed solvent of N,N-dimethylformam...

Embodiment 3

[0044] Preparation of PbS quantum dot ink

[0045] 1) Preparation of precursor solution: 55 g (0.12 mmol) of lead iodide, 4.56 mg (0.02 mmol) of N,N-diphenylthiourea and 9 mL of N,N-dimethylformamide were added to a 20 mL single port Stir in the flask at room temperature until the precursor is completely dissolved to obtain a precursor solution for use; the molar ratio of lead iodide to N,N-diphenylthiourea is 6:1, and the amount of the substance is 0.012M;

[0046] 2) Inject 1mL of butylamine into the one-necked flask, and continue stirring for 10 minutes. Transfer the reaction solution to a centrifuge tube, add toluene until the reaction solution becomes turbid, centrifuge at a speed of 8000 rpm, and discard the supernatant after centrifugation for 5 minutes; drain the obtained product under vacuum to prepare the obtained PbS quantum Store some ink in the glove box.

[0047] According to the technical scheme of this embodiment, the molar ratio of lead iodide to N,N-dipheny...

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Abstract

The invention relates to a direct synthesis method for preparing size-adjustable lead chalcogen quantum dots and its application. Mix the lead halide, the chalcogen precursor and the solvent, and dissolve it completely to obtain the precursor solution; add butylamine, continue the reaction at a temperature of 0°C to 100°C, add a non-polar solvent to precipitate, and then centrifuge The supernatant liquid was discarded and vacuum-dried to obtain lead chalcogen quantum dots, which were applied to solar cells. The present invention directly synthesizes lead-chalcogen quantum dots with adjustable size in one step by adjusting the concentration of lead and chalcogen precursors and different solvents under the action of butylamine, which solves the limitation that the size of the direct synthesis of quantum dot ink cannot be adjusted. Quantum dots with a larger size control range can be obtained, and the synthesis of large-size quantum dots has achieved preliminary applications in solar cells.

Description

technical field [0001] The invention relates to the technical field of functional materials, in particular to a direct synthesis of size-adjustable PbS quantum dots and the application of large-size quantum dots in solar cells. Background technique [0002] The PbX (X=S, Se, Te) of the IV-VI group has a large Bohr radius, which makes their quantum confinement effect particularly significant. Through size adjustment, the band gap of the quantum dot material can be greatly adjusted, and Its absorption spectrum is well matched with the solar spectrum reaching the earth's surface, and it also has properties such as large absorption coefficient, high electron mobility, and adjustable energy level, making IV-VI quantum dots the most popular photovoltaic nanometer in current research. material, which is expected to become a low-cost and high-efficiency solar cell for a new generation of solution process. [0003] At present, lead chalcogenide quantum dots need to use long-chain or...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C09K11/66C09K11/88C01G21/21B82Y40/00B82Y20/00H01L51/42
CPCC09K11/661C09K11/881B82Y20/00B82Y40/00C01G21/21H10K30/10Y02E10/549
Inventor 马万里刘洋刘泽柯
Owner SUZHOU UNIV