A perovskite solar cell using a perovskite composite material as a hole transport layer and its preparation method
A hole transport layer, perovskite-type technology, applied in circuits, electrical components, photovoltaic power generation, etc., can solve the problems of complex synthesis process, unfavorable commercial development of perovskite solar cells, and performance-price ratio gap. The effect of improving electrical conductivity, improving photoelectric conversion efficiency, and good electrical conductivity
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2018-11-27
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
technical field
[0001] The invention relates to a perovskite solar cell using a perovskite type material and a polypyrrole conductive polymer material as a hole transport layer and a preparation method thereof, belonging to the field of new energy and new materials. technical background
[0002] Perovskite solar cells are usually composed of five parts: transparent conductive glass, dense layer, perovskite light absorbing layer, hole transport layer, and metal back electrode. The thickness of the hole transport layer is generally 0-150nm. The photoelectric conversion efficiency of perovskite solar cells without a hole transport layer is usually relatively low. The functions of the hole transport layer include: (1) collecting light from the perovskite absorbing layer The injected holes separate the electron-hole pairs of the perovskite light-absorbing layer; (2) The insertion of the hole transport layer between the perovskite light-absorbing layer and the metal back electrode...
Examples
Embodiment 1
[0024] Add 220g (3.0mol) of dimethylformamide, 36g (0.3mol) of acetic acid and 6.7g (0.05mol) of pyrrole to a glass reactor to form an acidic solution of pyrrole, cool it to -5-5°C, and stir Slowly add 88.6g (0.10mol) of an acetic acid solution of lead tetraacetate with a concentration of 50% by mass, and carry out an oxidation reaction at 0-5°C for 8 hours to oxidize and polymerize pyrrole to form polypyrrole, and reduce lead tetraacetate to It is low-valence lead acetate. Then add 77.4 g (0.3 mol) of hydriodic acid solution with a concentration of 50% by mass and continue stirring for 1 hour to reduce excess lead tetraacetate to form a hydriodic acid-doped polypyrrole and lead iodide solution. Further add 10.3 g (0.1 mol) of a methanol solution of methylamine with a mass percent concentration of 30%, and react at 10-30°C for 8 hours to coordinate lead iodide with methylamine and polypyrrole in the presence of hydroiodic acid reaction to form a hole transport layer coating s...
Embodiment 2
[0028] Add 220g (3mol) of dimethylformamide, 36g (0.3mol) of acetic acid and 6.7g (0.05mol) of pyrrole to a glass reactor to form an acidic solution of pyrrole, cool it to -5-5°C, and stir Slowly add 28.7g (0.15mol) of an acetic acid solution of iron acetate with a concentration of 50% by mass, and carry out an oxidation reaction at 0-5°C for 12 hours to oxidize and polymerize pyrrole to form polypyrrole, and reduce iron acetate to low-priced state of iron acetate. Add 103.2 g (0.4 mol) of hydriodic acid solution with a mass percent concentration of 50% and continue stirring for 1 hour to reduce excess iron acetate to form a hydriodic acid-doped polypyrrole and ferrous iodide solution. Further add 15.5 g (0.15 mol) of methanol solution of methylamine with a concentration of 30% by mass, and react at 10-30°C for 12 hours to make ferrous iodide, methylamine and polypyrrole complex in the presence of hydroiodic acid bit reaction to form a hole transport layer coating solution. ...