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Preparation method for transparent organic and inorganic hybridization heterojunction material

A heterojunction and hybrid technology, which is applied in the field of transparent organic-inorganic hybrid heterojunction materials and their preparation, can solve the problems of adverse effects on photophysical properties, solubility, harsh reaction conditions, and easy aggregation of inorganic nanocrystals. Effects of improving dispersion stability and interface compatibility, increasing carrier life, and improving absorption efficiency

Inactive Publication Date: 2012-10-03
HEFEI UNIV OF TECH
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AI Technical Summary

Problems solved by technology

The energy conversion efficiency of hybrid heterojunction cells prepared by thiophene derivatives and inorganic acceptor materials has reached more than 7%. Most of the hybrid heterojunctions prepared by thiophene derivatives and inorganic semiconductors in current literature reports are physically blended ( U.S. Patent 7777303, Chinese Patent 101029142A, J.Phys.Chem.C, 2012, 116, 3153, etc.), this method cannot solve the problem of organic-inorganic two-phase compatibility, and inorganic nanocrystals are easy to agglomerate, which hinders the transmission of electrons. The phase separation between phases also affects the separation and transmission of excitons at the interface, making it difficult to fully exert its photoelectric properties
In order to solve the dispersion problem of inorganic nanocrystalline materials in conjugated polymer solutions, the introduction of polar functional groups into the conjugated polymer molecular chain can improve the dispersion stability of inorganic nanocrystals in conjugated polymer solutions, which is beneficial to the interface charge. Separation and transfer (as reported in the document J.Am.Chem.Soc.2004,126,6550), the reaction conditions of this type are usually harsh, and the introduction of polar functional groups has a negative impact on the photophysical properties of organic conjugated polymers and in organic solvents. There are adverse effects on the solubility and other aspects of
It is also possible to improve the dispersion and stability of nanocrystals by organically modifying the surface of nanocrystals, but it also becomes an insulating layer in optoelectronic devices that hinders the transfer of charges between donors and acceptors. The chelation exchange of such organic modifiers is a relatively effective method (as reported in the literature J.Phys.Chem.C, 2010, 114, 12784), but it has not played a role in improving the interface properties with polythiophene derivatives. to significant effect

Method used

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  • Preparation method for transparent organic and inorganic hybridization heterojunction material
  • Preparation method for transparent organic and inorganic hybridization heterojunction material
  • Preparation method for transparent organic and inorganic hybridization heterojunction material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] Example 1: Preparation of 3-hexylthiophene-pyridine copolymer and cadmium selenide (CdSe) hybrid heterojunction material

[0026] The preparation of step 1,3-hexylthiophene-pyridine copolymer:

[0027] Under the protection of nitrogen, add 2mmol magnesium wire, 1mmol 2,5-dibromo-3-hexylthiophene and 40ml anhydrous tetrahydrofuran into a dry three-necked flask, and react under reflux for 3h to prepare 3-hexylthiophene dimagnesium bromide. In the above reaction, 1 mmol of magnesium and 1 mmol of 2,5-dibromo-3-hexylthiophene can be fed to prepare 3-hexylthiophene magnesium bromide. Its reaction formula is as follows respectively:

[0028]

[0029] Mix 1 mmol 3-hexylthiophene magnesium bromide, 1 mmol 2,5-dibromopyridine and 1 mmol 3-hexylthiophene magnesium bromide, and add 0.035 mmol 1,3-bisdiphenylphosphinopropane nickel dichloride (Ni (dppp)Cl 2 ) catalyst for coupling reaction, the coupling reaction formula is as follows:

[0030]

[0031] Stir at room temper...

Embodiment 2

[0039] Example 2: Preparation of 3-hexylthiophene-pyridine copolymer and cadmium sulfide (CdS) hybrid heterojunction

[0040] The preparation of step 1,3-hexylthiophene-pyridine copolymer:

[0041] See Example 1 for the preparation of 3-hexylthiophene magnesium bromide, mix 1mmol 3-hexylthiophene magnesium bromide and 1mmol 2,5-dibromopyridine, and add 0.02mmol Ni(dppp)Cl at the same time 2 Catalyst carries out coupling reaction, and its reaction formula is as follows:

[0042] Stir at room temperature for 6 hours, then pour the above reaction solution into 40ml of methanol at room temperature to settle, centrifuge, and vacuum-dry the obtained solid at 40-50°C, extract with methanol, n-hexane, and chloroform in sequence, and then rotary evaporate to obtain reddish-brown 3 -hexylthiophene-pyridine copolymer, yield 60%.

[0043] Step 2, preparation of cadmium sulfide (CdS) nanocrystals:

[0044] Weigh 0.5mmol of CdO and 5mmol of sulfur powder into a three-necked bottle, add...

Embodiment 3

[0047] Example 3: Preparation of 3-hexylthiophene-pyridine copolymer and zinc oxide (ZnO) hybrid heterojunction

[0048] The preparation of step 1,3-hexylthiophene-pyridine copolymer:

[0049] Under the protection of nitrogen, add 2.5mmol of 2,5-dibromo-3-hexylthiophene, 5.0mmol of isopropylmagnesium chloride Grignard reagent and 50ml of anhydrous tetrahydrofuran into a dry three-necked flask, and react at 0°C for 1h to obtain 3- Hexylthiophene Magnesium Chloride and 3-Hexylthiophene Magnesium Chloride. Its reaction formula is as follows:

[0050]

[0051] Add 1.0mmol of 2,5-dibromopyridine to the above reaction system, then add 0.035mmol of Ni(dppp)Cl 2 Catalyst carries out coupling reaction, and its reaction formula is as follows:

[0052]

[0053] Stir at room temperature for 12 h to obtain a reaction solution. Pour the reaction solution into 50ml of methanol at room temperature to settle and centrifuge. The resulting solid is vacuum-dried at 40-50°C, extracted wi...

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Abstract

The invention discloses a transparent organic and inorganic hybridization heterojunction material and a preparation method thereof. According to the heterojunction material, alkylthrophene-pyridine copolymer which is used as a p-type semiconductor material and II-VI group inorganic nanocrystalline which is used as an n-type semiconductor material are assembled in a solution, and then a film is formed by a spin coating, casting or printing method; and room-temperature large-area forming can be realized. The prepared hybridization heterojunction is ordered in structure and high in light absorption efficiency, dispersion stability and interfacial compatibility. Films formed by the hybridization heterojunction materials are high in light transmission and can widely used as materials of various active coatings in semiconductor photoelectric devices.

Description

technical field [0001] The invention belongs to the field of photoelectric device materials, and in particular relates to a transparent organic-inorganic hybrid heterojunction material and a preparation method thereof. Background technique [0002] Semiconductor optoelectronic devices can realize the exchange of light and electricity and are widely used in information, lighting, energy and other fields. The commonly used materials are semiconductor silicon, germanium, inorganic compounds, etc., which can be manufactured by interfacial alloys, epitaxial growth, vacuum deposition and other technologies. Heterojunction has the disadvantages of high cost, complex process, toxicity in the manufacturing process, and difficult flexible processing. Conjugated polymers have the advantages of light weight, flexibility, low cost, and can be chemically modified to control their properties. They can be formed into large-area films by solution spin coating, casting, etc., and show great p...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08J5/18C08L65/00C08K3/22C08K3/30C08G61/12
Inventor 汪瑾罗小霞康达莲
Owner HEFEI UNIV OF TECH
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