Electrical storage device based on one-dimensional organic-inorganic hybrid polymer chain and preparation method thereof
A polymer chain and electric storage technology, which is applied in the fields of electric solid-state devices, semiconductor/solid-state device manufacturing, electrical components, etc., can solve the problems of low ternary yield of devices, poor high temperature stability, high turn-on voltage, etc. High yield, high temperature stability, and low turn-on voltage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0044] A preparation method of an organic-inorganic hybrid polymer, the specific synthesis steps are as follows:
[0045]2,5-diamino-1,4-benzenedithiol dihydrochloride (245.2 mg, 1 mmol) was dissolved in DMF (50 mL), and dry nitrogen was passed through for 5 hours to remove dissolved oxygen in the solvent, and then Zinc dichloride (136.3 mg, 1 mmol) was dissolved in deionized water (50 mL) and added dropwise to the above solution at 0 °C. Then the reaction system was adjusted to neutrality (pH = 7) by adding ammonia water dropwise. Finally, it was stirred at room temperature for 6 h. After the reaction, a black solid was formed. The reaction solution was evaporated under reduced pressure to remove the solvent, and then the solid was washed with water and acetone respectively. After repeating the above steps three times, it was dried in a vacuum oven at 70°C for 12 hours, and finally a brown powder product was obtained. Organic-inorganic hybrid polymer, denoted as Zn-DABDT. ...
Embodiment 2
[0047] A preparation method of an organic-inorganic hybrid polymer, the specific synthesis steps are as follows:
[0048] 2,5-diamino-1,4-benzenedithiol dihydrochloride (245.2 mg, 1 mmol) was dissolved in DMF (50 mL), and dry nitrogen was passed through for 5 hours to remove dissolved oxygen in the solvent, and then Copper sulfate pentahydrate (249.7 mg, 1 mmol) was dissolved in deionized water (50 mL) and added dropwise to the above solution at 0 °C. Then the reaction system was adjusted to neutrality (pH = 7) by adding ammonia water dropwise. Finally, it was stirred at room temperature for 6 h. After the reaction, a black solid was formed. The reaction solution was evaporated under reduced pressure to remove the solvent, and then the solid was washed with water and acetone respectively. After repeating the above steps three times, it was dried in a vacuum oven at 70°C for 12 hours, and finally a black powder product was obtained. Recorded as Cu-DABDT.
Embodiment 3
[0050] A preparation method of an organic-inorganic hybrid polymer, the specific synthesis steps are as follows:
[0051] 2,5-diamino-1,4-benzenedithiol dihydrochloride (245.2 mg, 1 mmol) was dissolved in DMF (50 mL), and dry nitrogen was passed through for 5 hours to remove dissolved oxygen in the solvent, and then Nickel dichloride hexahydrate (237.7 mg, 1 mmol) was dissolved in deionized water (50 mL) and added dropwise to the above solution at 0 °C. Then the reaction system was adjusted to neutrality (pH = 7) by adding ammonia water dropwise. Finally, it was stirred at room temperature for 6 h. After the reaction, a black solid was formed. The reaction solution was evaporated under reduced pressure to remove the solvent, and then the solid was washed with water and acetone respectively. After repeating the above steps three times, it was dried in a vacuum oven at 70°C for 12 hours, and finally a black powder product was obtained. Denoted as Ni-DABDT.
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com