Large-area perovskite solar cell composite photoelectric conversion layer and preparation method therefor
A photoelectric conversion layer and photoelectric conversion technology, applied in the direction of circuits, photovoltaic power generation, electrical components, etc., can solve the problems of not meeting the requirements of engineering coating, poor film-forming performance of perovskite photoelectric conversion materials, etc., and achieve extended absorption Effect of wavelength range
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Embodiment 1
[0031] Coating nano-TiO with a thickness of 20-50nm on a 100mm×100mm FTO conductive glass substrate 2 Dense layer, then coated with TiO with a particle size of 40-60nm and a thickness of 100-600nm 2 The thin film is finally sintered at 450-550° C. to form the skeleton layer of the photoelectric conversion layer. Weigh CH 3 NH 3 PB 3 Dissolve 5 g of perovskite photoelectric conversion materials in 30 g of dehydrated dimethylformamide solvent, stir for 12 hours until completely dissolved, and filter through a biscuit ceramic funnel to form a photoelectric conversion material with a concentration of 14.3% by mass Solution, use a stainless steel wire bar coater to coat the photoelectric conversion material solution on the photoelectric conversion layer skeleton, and form a methylamine iodide lead CH with a thickness of 300nm after the solvent evaporates. 3 NH 3 PB 3 Photoelectric conversion material crystalline thin film.
[0032] Add 300g of dimethylformamide, 63.7g (0.21m...
Embodiment 2
[0036] Add 300g of hexamethylphosphoric triamide, 63.7g (0.21mol) of hydroiodic acid with a mass percent concentration of 50% and 37.3g (0.1mol) of stannous iodide in a glass reactor, at 40-60°C Stir until completely dissolved, then add 13.6g (0.105mol) of cyanuric acid, continue to stir and react for 16 h, and obtain iodide stannous cyanurate C 3 N 3 h 2 o 3 SnI 4 solution; concentrated in vacuum to the solution in which crystallization is precipitated, adding absolute ethanol to make the iodide stannous cyanurate C dissolved in the polar solvent 3 N 3 h 2 o 3 SnI 4 Precipitate out, vacuum filter, absolute ethanol washing, vacuum drying to obtain refined iodide stannous cyanurate C 3 N 3 h 2 o 3 SnI 4 72.5 g of crystals were obtained, and the yield was 96%. The iodide stannous cyanurate C prepared above 3 N 3 h 2 o 3 SnI 4 Crystallization 5g, be dissolved in the hexamethylphosphoric triamide solvent of 30g through the dehydration process, finely filter with ...
Embodiment 3
[0040] Add 300g of dimethyl sulfoxide, 63.7g (0.21mol) of hydroiodic acid with a mass percent concentration of 50% and 46.1g (0.1mol) of lead iodide into a glass reactor, and stir at 40-60°C until completely Dissolve, then add 17.7g (0.10mol) of tripolythiocyanate, continue to stir and react for 24 h to obtain iodide lead tripolythiocyanate C 3 h 5 N 3 S 3 PB 4 solution; concentrated in vacuum to the solution with crystallization, adding absolute ethanol to make the iodide lead tripolythiocyanate C dissolved in the polar solvent 3 h 5 N 3 S 3 PB 4 Precipitated, vacuum filtered, washed with absolute ethanol, vacuum dried to obtain refined iodide lead tripolythiocyanate C 3 h 5 N 3 S 3 PB 4 88.5 g of crystals were obtained, and the yield was 99%. The above-prepared iodide lead thiocyanate C 3 h 5 N 3 S 3 PB 4 Crystallization 5g, be dissolved in 30g through the dimethyl sulfoxide solvent of dehydration treatment, finely filter with bisque ceramic funnel, will be...
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