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Preparation method of fluorene block thiophene cathode interface layer containing silane terminal group

A cathode interface layer and terminal group technology, which is applied in semiconductor/solid-state device manufacturing, photovoltaic power generation, electrical components, etc., can solve the problem of poor morphology of the upper active layer, large interface barrier between the active layer and the electrode, and poor mechanical properties of the interface layer and other problems, to achieve the effect of improving the morphology, improving the mechanical properties, and improving the film-forming property

Pending Publication Date: 2018-08-24
NANCHANG HANGKONG UNIVERSITY
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Problems solved by technology

[0004] In order to overcome the deficiencies of the above prior art, the present invention provides a method for preparing a fluorene block thiophene cathode interface layer containing silane end groups; the existing cathode interface layer is a random or alternating conjugated polymer electrolyte, rich in These cathode interfacial layers cannot simultaneously solve the problems of large interfacial barrier between the active layer and the electrode, poor morphology of the upper active layer and poor mechanical properties of the interfacial layer.

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  • Preparation method of fluorene block thiophene cathode interface layer containing silane terminal group
  • Preparation method of fluorene block thiophene cathode interface layer containing silane terminal group
  • Preparation method of fluorene block thiophene cathode interface layer containing silane terminal group

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Embodiment Construction

[0017] The present invention will be further described below in conjunction with the accompanying drawings.

[0018] The reaction equation of the present invention is attached figure 2 , the specific reaction steps are as follows:

[0019] Fluorene block thiophene PF with silane terminal groups EO - b -Synthetic steps of PTSi:

[0020] (1) Synthesis of compound 1: Add 2.5 g, 22.0 mmol 3-thiophene methanol and 60 mL anhydrous tetrahydrofuran solution in a dry 250 mL round-bottom flask, then add 7.9 g, 44.0 mmol NBS in batches, and react overnight in the dark . Remove the NBS remaining in the reaction by filtration, remove the tetrahydrofuran solvent by a rotary evaporator, extract the product with 200 mL of ether and water, and wash with 1M sodium hydroxide solution, combine the organic layer products, and spin dry the obtained crude product with n-hexane: acetic acid The volume ratio of ethyl ester was 3:1, purified by column, and dried with anhydrous magnesium sulfate t...

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Abstract

The invention discloses a preparation method of a fluorene block thiophene cathode interface layer containing a silane terminal group. The preparation method comprises the steps: firstly, carrying outtransfer coupling polymerization on 9,9-bis(2'-(2'-(2'-methoxyl)ethyoxyl)ethyl)-2,7-dibromofluorene and 3-(6-((2,5- dibromothiophene)-3-methoxyhexyl)-1,1,1,3,5,5,5-hexamethylsilane by using a Kumadacatalyst to obtain a target block polymer PFEO-b-PTSi; and settling the polymer by using n-hexane, extracting the polymer by using a Soxhlet extractor, passing a column by using neutral alumina, and drying the polymer to obtain a faint yellow fluffy solid. A side chain contains a polar oxyalkyl chain and a siloxyl chain, so that the block polymer is not only capable of realizing the processing ofa polar solvent such as water and alcohols and reducing the work functions, good in mechanical performance and environment-friendly, but also capable of improving the shape of an active layer on an upper layer. The fluorene block thiophene cathode interface layer containing silane terminal group can be used as an excellent cathode interface layer of a device such as an organic photovoltaic cell, alight emitting diode and an FET.

Description

technical field [0001] The invention relates to the technical field of cathode interface of organic solar cells, in particular to a preparation method of a fluorene block thiophene cathode interface layer containing silane end groups. Background technique [0002] With the increasingly severe global environmental pollution and scarcity of resources, it is imminent to develop renewable and clean energy. Among all renewable energy sources, solar energy stands out for its advantages of abundant resources, cleanliness, and limited geographical location. At present, the commercialized solar cells are mainly inorganic silicon solar cells, but due to the complex production process, expensive production equipment, limited silicon materials, and the conversion efficiency has basically reached the limit, its further large-scale commercialization is subject to greater challenges. limit. However, organic thin-film solar cells are favored by scholars at home and abroad because they can...

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Application Information

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IPC IPC(8): C08G61/12H01L51/46
CPCC08G61/02C08G61/126C08G2261/91C08G2261/51C08G2261/64C08G2261/62C08G2261/3142C08G2261/3223C08G2261/126C08G2261/1424C08G2261/144H10K85/113H10K85/1135Y02E10/549
Inventor 周丹徐镇田秦元成郑夏
Owner NANCHANG HANGKONG UNIVERSITY
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