CN101114696A - Process for producing polymer solar battery - Google Patents
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- CN101114696A CN101114696A CN 200710055979 CN200710055979A CN101114696A CN 101114696 A CN101114696 A CN 101114696A CN 200710055979 CN200710055979 CN 200710055979 CN 200710055979 A CN200710055979 A CN 200710055979A CN 101114696 A CN101114696 A CN 101114696A
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Abstract
The invention belongs to a method producing solar cell by polymer, greatly improving crystallinity of P3HT in a blending film of a P3HT and C60 fullerene or a derivative PCBM of P3HT and ensuring whisker of P3HT in the blending film which is in a micro length to be uniformly dispersed on the whole film and having a nano-sized separation distance. By using the method, the transferring efficiency of solar cell arrives at 3.9 percent while the transferring efficiency of solar cell processed by thermal annealing can only reach 3.7 percent, which shows that through the method the high performed and non-annealed polymer solar cell can be produced by one step.
Description
Technical field
The present invention relates to a kind of preparation method of polymer solar battery, be specifically related to a kind of by exempting from the method for annealing way preparation based on the polymer solar battery of polythiophene/fullerene and derivative blended film thereof.
Background technology
Polymer solar battery is because advantages such as its cheapness, flexibility, large tracts of land become a focus of cleaning, regenerative resource research field in recent years.In polymer solar battery based on soluble poly thiophene (P3HT)/fullerene and derivative blended film thereof, the polythiophene that makes up high crystalline (the Advanced FunctionalMaterials 2003 that often efficient of battery is greatly improved, 13,85; Nature Materials 2005,4,864).Traditionally, the method that often adopts after annealing to handle improves the degree of crystallinity of polythiophene in the device.But this method causes producing being separated of large scale (more than the micron order) in the film between the blend components easily, is unfavorable for the raising of device performance.In addition, during (＞100 ℃) thermal annealing, there is the risk of polythiophene oxidation, degraded under the higher temperature, may makes battery failure.In polymer solar battery, utilize the pattern of the method regulation and control blend film of mixed solvent can significantly improve the efficient (Nature Materials 2007,6,497) of battery based on amorphous conjugated polymer/fullerene.Because the crystallizability of P3HT, regulate and control its crystal property more complicated and difficulty in blend film by mixed solvent, so the example that utilizes the method for mixed solvent to improve P3HT/ fullerene and derivative polymer solar cell device efficient thereof does not appear in the newspapers as yet.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of polymer solar battery.By in solution, make up ordered aggregation improve poly-(3-hexyl) thiophene (P3HT) with C
60And derivative [6,6]-C
61Degree of crystallinity in-phenylbutyric acid methyl esters (PCBM) blend film.
Polymer solar battery P3HT/PCBM and P3HT/C that this method is prepared
60Blend film need not promptly to have realized high P3HT degree of crystallinity by back thermal anneal process or solvent annealing in process, formed P3HT whisker be dispersed in the film and with PCBM or C
60Form inierpeneirating network structure, composite material is separated yardstick at nanoscale, and the conversion efficiency of obtained device is suitable under its photoelectric conversion efficiency and the thermal annealing condition under white light.Thereby this method " a step " realized the solar cell device that high-performance " is exempted from annealing ", simplified the manufacturing procedure of polymer solar battery greatly, and eliminated the risk of other component oxidation, degraded in the device.
A kind of preparation method's of polymer solar battery step and condition are as follows:
Under the room temperature, P3HT is dissolved under stirring condition in good solvent o-dichlorohenzene (ODCB), chloroform (CF) or the chlorobenzene (CB), preferred o-dichlorohenzene (ODCB) solvent is made into the solution of 5～10 mg/ml; In the solution of above-mentioned gained, divide slowly dropping poor solvent 5-15 time then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, poor solvent is a n-hexane, cyclohexane, alcohol or acetone, the interpolation total amount of poor solvent is 0.2～1 milliliter of poor solvent/milliliter good solvent, drip at every turn poor solvent with relief solution under 100～500rpm mixing speed, stirred 10-60 minute, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 100～500rpm, carry out 6-24 hour, add in the solution again and be equivalent to the C that quality is measured by molten P3HT in 0.5～2 times of solution in the dark place
60Or derivatives thereof PCBM, and under the mixing speed of 200～1000rpm, stirred 2-16 hour, be made into P3HT: PCBM or P3HT: C
60Mass ratio is 1: 2～2: 1 a mixed solution, at last gained solution is got rid of the film machine with rotation and carries out spin coating system film, obtains a kind of polymer solar battery behind the electrode evaporation.
Shown in Fig. 1 b, the P3HT whisker that reaches several microns in the preparation-obtained P3HT/PCBM blend film of the present invention is evenly distributed in the whole film, and the corynebacterium crystal of the P3HT that obtains from ODCB solution with Fig. 1 a makes a sharp contrast.Secondly, be inserted in the outer shroud electronic diffraction intensity that belongs to P3HT (020) crystal face in the picture by contrast, can reach a conclusion: the degree of crystallinity by P3HT in the P3HT/PCBM blend film of the method preparation that the present invention introduced is than with simple ODCB much higher as in the prepared blend film of solvent.Once more, the yardstick that is separated among Fig. 1 b is in nanometer scale, the whisker and the PCBM matrix of the formed micron order length of P3HT are built into interpenetrating networks, this separation for exciton provides huge interface, and provide continuous path for the transmission of charge carrier, reduce the loss of charge carrier in the transmission course, helped improving the efficient of solar cell.
Use the prepared polymer solar battery of method of the present invention, under condition without any reprocessing, its conversion efficiency has reached 3.9%, ratio is by taller with 3.7% efficient that obtains in the device of ODCB as the process thermal anneal process of solvent preparation merely, see Fig. 4, in detail relatively see Table 1.In addition, family device studies show that: utilizing the average efficiency without any reprocessing device of the method for the invention preparation is 3.3%, this is than the 3.1% average efficiency height that obtains in the thermal anneal process by the back, has realized " one-step method " preparation high-performance polymer solar battery of " exempting from annealing ".
Relatively (wave-length coverage is 400-900nm to the performance that table 1. utilizes the polymer solar battery that distinct methods prepares after Schott KG1 and GG385 filter filter, and maximum transmission power is at the 40mW/cm of 650nm
2In air, measure under the tungsten halogen lamp illuminate condition).
| Device parameters | Short-circuit current density J sc (mA/cm 2) | Open circuit voltage V oc (V) | Fill factor, curve factor FF | Conversion efficiency PCE (%) | Cell area (mm 2) |
| Original device | 1.47 | 0.64 | 0.46 | 1.08 | 7.5 |
| The annealing device | 4.80 | 0.59 | 0.52 | 3.68 | 7.5 |
| The device of the present invention's preparation | 6.00 | 0.50 | 0.52 | 3.90 | 6.0 |
Description of drawings
Fig. 1 is that the P3HT/PCBM mass ratio is the transmission electron micrograph of 1: 1 blend film.Use the preparation-obtained blend film of the inventive method (Fig. 1 b) P3HT whisker and reach the micron number magnitude, and be evenly distributed, do not have the appearance that is separated of large scale.Simultaneously, by comparing both original position electronic diffraction intensity, the external diffraction ring that can find to belong among Fig. 1 b (020) crystal face of P3HT obviously is better than merely the diffraction ring of P3HT in the blend film for preparing as solvent with ODCB, and this has shown that the method by make up ordered aggregation in solution can improve the degree of crystallinity of P3HT in the P3HT/PCBM blend film effectively.
Fig. 2 is the X-ray diffractogram of 1: 1 blend film for the P3HT/PCBM mass ratio, (1: the simple P3HT/PCBM blend film that makes as solvent with ODCB; 2: 30 minutes the P3HT/PCBM blend film of annealing under 120 ℃ of conditions that from pure ODCB solvent, makes; 3: the new system P3HT/PCBM blend film without any reprocessing that utilizes the present invention to prepare) it can make the degree of crystallinity of P3HT in blend film with similar through the degree of crystallinity of P3HT in the blend film for preparing as solvent with ODCB merely of thermal anneal process from showing utilization makes up ordered aggregation solution method on a large scale.
Fig. 3 is that the P3HT/PCBM mass ratio is ultraviolet (UV)-visible light (Vis) absorption figure (1: the simple P3HT/PCBM blend film that makes as solvent with ODCB of 1: 1 blend film; 2: 30 minutes the P3HT/PCBM blend film of annealing under 120 ℃ of conditions that from pure ODCB solvent, makes; 3: the new system P3HT/PCBM blend film without any reprocessing that utilizes the present invention to prepare), that uses blend film that the present invention the prepares blend film that its light absorption is crossed as solvent and through annealing in process with ODCB under the suitable situation of thickness as seen from the figure wants high.In addition, its absorption curve is at 607 nanometers (π-π between the P3HT strand
*Change, its appearance show have the P3HT crystallization) absworption peak more obvious, reflected the degree of crystallinity of using P3HT in the blend film that the present invention obtains later on and all obtained enhancing in the absorption of long-wave band (＞600 nanometer).
Fig. 4 is that 1: 1 polymer solar battery is at 40mW/cm for the P3HT/PCBM mass ratio
2The J-V characteristic curve of measuring in the air under the tungsten halogen lamp illuminate condition (1: the simple original device that makes as solvent with ODCB; 2: from pure ODCB solvent make through 30 minutes devices of 120 ℃ of annealing; 3: the device that utilizes the present invention to prepare).As seen from the figure, under the suitable situation of fill factor, curve factor (FF), to be higher than the short-circuit current density that obtains by in the thermal anneal process device by the short-circuit current density without the polymer solar battery of any reprocessing of the method for the invention preparation.
Embodiment
Embodiment 1: under the room temperature, P3HT is dissolved in good solvent o-dichlorohenzene (ODCB) under stirring condition, is made into the solution of 8.0 mg/ml; Divide slowly dropping poor solvent n-hexane 10 times then in the solution of above-mentioned gained, the addition of each poor solvent and the volume ratio of good solvent are 0.03: 1-0.1: 1, and it adds total amount is 0.5 ml n-hexane/milliliter ODCB solution.Drip at every turn poor solvent with relief solution under the 200rpm mixing speed, stirred 30 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 12 hours in the dark place, add in the solution again and be equivalent to the PCBM that quality is measured by molten P3HT in 1 times of solution, and under the mixing speed of 500rpm, stirred 6 hours, be made into P3HT: the PCBM mass ratio is 1: 1 a mixed solution, at last gained solution is got rid of the film machine with rotation and carry out spin coating system film, obtain a kind of polymer solar battery behind the electrode evaporation.The original device efficiency of gained is 3.9%.
Embodiment 2: under the room temperature, P3HT is dissolved in good solvent o-dichlorohenzene (ODCB) under stirring condition, is made into the solution of 10.0 mg/ml; Divide slowly dropping poor solvent cyclohexane 15 times then in the solution of above-mentioned gained, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 1 milliliter of cyclohexane/milliliter ODCB solution.Drip at every turn poor solvent with relief solution under the 100rpm mixing speed, stirred 10 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 100rpm, carry out 6 hours in the dark place, add in the solution again and be equivalent to the PCBM that quality is measured by molten P3HT in 0.5 times of solution, and under the mixing speed of 1000rpm, stirred 2 hours, be made into P3HT: the PCBM mass ratio is 2: 1 a mixed solution, at last gained solution is got rid of the film machine with rotation and carry out spin coating system film, obtain a kind of polymer solar battery behind the electrode evaporation.The original device average efficiency of gained is 2.9%.
Embodiment 3: under the room temperature, P3HT is dissolved in good solvent o-dichlorohenzene (ODCB) under stirring condition, is made into the solution of 5.0 mg/ml; Divide slowly dropping poor solvent alcohol 5 times then in the solution of above-mentioned gained, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.2 ml ethanol/milliliter ODCB solution.Drip at every turn poor solvent with relief solution under the 500rpm mixing speed, stirred 60 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 500rpm, carry out 24 hours in the dark place, add in the solution again and be equivalent to the PCBM that quality is measured by molten P3HT in 2 times of solution, and under the mixing speed of 200rpm, stirred 16 hours, be made into P3HT: the PCBM mass ratio is 1: 2 a mixed solution, at last gained solution is got rid of the film machine with rotation and carry out spin coating system film, obtain a kind of polymer solar battery behind the electrode evaporation.The original device average efficiency of gained is 2.8%.
Embodiment 4: under the room temperature, P3HT is dissolved under stirring condition in o-dichlorohenzene (ODCB) solvent, be made into the solution of 7.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent acetone (acetone) 8 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.4 milliliter of/milliliter ODCB solution.Drip at every turn poor solvent with relief solution under the 300rpm mixing speed, stirred 40 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 12 hours in the dark place, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.Last prepared original device average efficiency is 3.2%.
Embodiment 5: under the room temperature, P3HT is dissolved under stirring condition in chloroform (CF) solvent, be made into the solution of 8.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent n-hexane 9 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.5 ml n-hexane/milliliter CF solution.Drip at every turn poor solvent with relief solution under the 300rpm mixing speed, stirred 30 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 16 hours in the dark place, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.Last prepared original device average efficiency is 3.0%.
Embodiment 6: under the room temperature, P3HT is dissolved under stirring condition in chloroform (CF) solvent, be made into the solution of 10.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent cyclohexane 12 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.04: 1-0.1: 1, and it adds total amount is 1.0 milliliters of cyclohexanes/milliliter CF solution.Drip at every turn poor solvent with relief solution under the 400rpm mixing speed, stirred 40 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 300rpm, carry out 24 hours in the dark place, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.The average efficiency of last prepared original polymer solar cell is 3.1%.
Embodiment 7: under the room temperature, P3HT is dissolved under stirring condition in chloroform (CF) solvent, be made into the solution of 5.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent alcohol (alcohol) 5 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.2 ml ethanol/milliliter CF solution.Drip at every turn poor solvent with relief solution under the 500rpm mixing speed, stirred 30 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 100rpm, carry out 10 hours in the dark place.Remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.Last prepared original device average efficiency is 3.0%.
Embodiment 8: under the room temperature, P3HT is dissolved under stirring condition in chloroform (CF) solvent, be made into the solution of 8.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent acetone (acetone) 6 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.3 milliliter of acetone/milliliter CF solution.Drip at every turn poor solvent with relief solution under the 500rpm mixing speed, stirred 40 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 16 hours in the dark place, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.The average efficiency of last prepared original polymer solar cell is 2.9%.
Embodiment 9: under the room temperature, P3HT is dissolved under stirring condition in chlorobenzene (CB) solvent, be made into the solution of 8.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent n-hexane (hexane) 10 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.5 ml n-hexane/milliliter CB solution.Drip at every turn poor solvent with relief solution under the 300rpm mixing speed, stirred 50 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 100rpm, carry out 6 hours in the dark place.Remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.The average efficiency of last prepared original polymer solar cell is 3.2%.
Embodiment 10: under the room temperature, P3HT is dissolved under stirring condition in chlorobenzene (CB) solvent, be made into the solution of 6.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent cyclohexane (cyclohexane) 10 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.04: 1-0.1: 1, and it adds total amount is 0.8 milliliter of cyclohexane/milliliter CB solution.Drip at every turn poor solvent with relief solution under the 400rpm mixing speed, stirred 30 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 12 hours in the dark place, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 3.The average efficiency of last prepared original polymer solar cell is 2.9%.
Embodiment 11: under the room temperature, P3HT is dissolved under stirring condition in chlorobenzene (CB) solvent, be made into the solution of 10.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent alcohol (alcohol) 5 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.3 ml ethanol/milliliter CB solution.Drip at every turn poor solvent with relief solution under the 500rpm mixing speed, stirred 30 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 18 hours in the dark place, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 2.The average efficiency of last prepared original polymer solar cell is 3.0%.
Embodiment 12: under the room temperature, P3HT is dissolved under stirring condition in chlorobenzene (CB) solvent, be made into the solution of 8.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent acetone (acetone) 10 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.04: 1, and it adds total amount is 0.3 milliliter of acetone/milliliter CB solution.Remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 1.The average efficiency of last prepared original polymer solar cell is 3.0%.
Embodiment 13: under the room temperature, P3HT is dissolved under stirring condition in o-dichlorohenzene (ODCB) solvent, be made into the solution of 8.0 mg/ml, in the solution of above-mentioned gained, divide slowly dropping poor solvent n-hexane (hexane) 10 times then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.5 ml n-hexane/milliliter ODCB solution.Drip at every turn n-hexane with relief solution under the 200rpm mixing speed, stirred 40 minutes P3HT reaches dissolution equilibrium in the solution so that make.After adding last poor solvent, allow solution under the mixing speed of 200rpm, place 24 hours, add in the solution again and be equivalent to the C of quality by the amount of molten P3HT in 1 times of solution
60, and under the 1000rpm mixing speed, stir and be made into P3HT: C in 16 hours
60Mass ratio be 1: 1 mixed solution.With gained solution spin coating system film, obtain a kind of polymer solar battery behind the electrode evaporation at last.Prepared is 2.2% without the original device average efficiency of any reprocessing.
Embodiment 14: under the room temperature, P3HT is dissolved under stirring condition in chlorobenzene (CB) solvent, is made into the solution of 6.0 mg/ml, remaining concrete steps obtains a kind of polymer solar battery as described in the embodiment 13.Last prepared original device average efficiency is 2.0%.
Embodiment 15: under the room temperature, P3HT is dissolved in good solvent o-dichlorohenzene (ODCB) under stirring condition, is made into the solution of 10.0 mg/ml; Divide slowly dropping poor solvent cyclohexane 12 times then in the solution of above-mentioned gained, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 1 milliliter of cyclohexane/milliliter ODCB solution.Drip at every turn poor solvent with relief solution under the 300rpm mixing speed, stirred 30 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 100rpm, carry out 8 hours, add in the solution again and be equivalent to the C that quality is measured by molten P3HT in 0.5 times of solution in the dark place
60, and under the mixing speed of 800rpm, stirred 8 hours, be made into P3HT: C
60Mass ratio is 2: 1 a mixed solution, at last gained solution is got rid of the film machine with rotation and carries out spin coating system film, obtains a kind of polymer solar battery behind the electrode evaporation.The original device average efficiency of gained is 2.0%.
Embodiment 16: under the room temperature, P3HT is dissolved in good solvent o-dichlorohenzene (ODCB) under stirring condition, is made into the solution of 5.0 mg/ml; Divide slowly dropping poor solvent n-hexane 10 times then in the solution of above-mentioned gained, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, and it adds total amount is 0.5 ml n-hexane/milliliter ODCB solution.Drip at every turn poor solvent with relief solution under the 300rpm mixing speed, stirred 40 minutes, so that make the P3HT in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 200rpm, carry out 12 hours, add in the solution again and be equivalent to the C that quality is measured by molten P3HT in 0.5 times of solution in the dark place
60, and under the mixing speed of 500rpm, stirred 10 hours, be made into P3HT: C
60Mass ratio is 1: 2 a mixed solution, at last gained solution is got rid of the film machine with rotation and carries out spin coating system film, obtains a kind of polymer solar battery behind the electrode evaporation.The original device average efficiency of gained is 1.8%.
Claims (2)
1. the preparation method of a polymer solar battery is characterized in that, step and condition are as follows: under the room temperature, will gather (3-hexyl) thiophene and be dissolved in good solvent o-dichlorohenzene, chloroform or the chlorobenzene under stirring condition, and be made into the solution of 5～10 mg/ml; In the solution of above-mentioned gained, divide slowly dropping poor solvent 5-15 time then, the addition of each poor solvent and the volume ratio of good solvent are 0.02: 1-0.1: 1, poor solvent is n-hexane, cyclohexane, alcohol or acetone, and the interpolation total amount of poor solvent is 0.2～1 milliliter of poor solvent/milliliter good solvent.Drip at every turn poor solvent with relief solution under 100～500rpm mixing speed, stirred 10-60 minute, so that make poly-(3-hexyl) thiophene in the solution reach dissolution equilibrium, after adding last poor solvent, allow solution under the mixing speed of 100～500rpm, carry out 6-24 hour, add in the solution again and be equivalent to the C that quality is (3-hexyl) the thiophene amount that contains intermingle with in 0.5～2 times of solution in the dark place
60Or derivatives thereof [6,6]-C
61-phenylbutyric acid methyl esters, and under the mixing speed of 200～1000rpm, stirred 2-16 hour, be made into poly-(3-hexyl) thiophene: [6,6]-C
61-phenylbutyric acid methyl esters or poly-(3-hexyl) thiophene: C
60Mass ratio is 1: 2～2: 1 a mixed solution, at last gained solution is got rid of the film machine with rotation and carries out spin coating system film, obtains a kind of polymer solar battery behind the electrode evaporation.
2. the preparation method of a kind of polymer solar battery as claimed in claim 1 is characterized in that, described good solvent is the o-dichlorohenzene solvent.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101494255B (en) * | 2009-03-05 | 2010-06-02 | 中国科学院长春应用化学研究所 | Preparation method for thin-film solar cell based on narrowband gap conjugated polymer |
| CN102347448A (en) * | 2011-06-28 | 2012-02-08 | 苏州大学 | Application of high-fullerene liquid crystal molecule as heterojunction solar battery receptor material |
| CN102623642A (en) * | 2012-03-22 | 2012-08-01 | 中国科学院长春应用化学研究所 | Preparation method of polymer solar cell |
| CN103811663A (en) * | 2014-02-27 | 2014-05-21 | 西南大学 | Annealed free organic solar cell and production method thereof |
| CN110993791A (en) * | 2019-12-09 | 2020-04-10 | 东华大学 | Method for regulating and controlling growth of conductive polymer film crystal |
| CN111247655A (en) * | 2017-10-23 | 2020-06-05 | 住友化学株式会社 | Photoelectric conversion element |
| CN112701225A (en) * | 2020-12-29 | 2021-04-23 | 深圳大学 | Stretchable photoelectric detector and preparation method thereof |
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| CN1129353A (en) * | 1995-02-16 | 1996-08-21 | 南京大学 | High-intensive conducting polythiophene thin film, thin-film diode and making method thereof |
| JP2001196664A (en) * | 2000-01-12 | 2001-07-19 | Japan Science & Technology Corp | Thin film material for generation and transfer of optical carrier of photoelectric conversion element comprising stereoregularity polythiophene derivative |
| US7262264B2 (en) * | 2005-01-12 | 2007-08-28 | Honeywell International Inc. | Halogenated thiophene monomer for the preparation of regioregular polythiophenes |
| CN100489020C (en) * | 2006-11-16 | 2009-05-20 | 中国科学院长春应用化学研究所 | High order polythiophene film and preparation process thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101494255B (en) * | 2009-03-05 | 2010-06-02 | 中国科学院长春应用化学研究所 | Preparation method for thin-film solar cell based on narrowband gap conjugated polymer |
| CN102347448A (en) * | 2011-06-28 | 2012-02-08 | 苏州大学 | Application of high-fullerene liquid crystal molecule as heterojunction solar battery receptor material |
| CN102623642A (en) * | 2012-03-22 | 2012-08-01 | 中国科学院长春应用化学研究所 | Preparation method of polymer solar cell |
| CN102623642B (en) * | 2012-03-22 | 2014-04-16 | 中国科学院长春应用化学研究所 | Preparation method of polymer solar cell |
| CN103811663A (en) * | 2014-02-27 | 2014-05-21 | 西南大学 | Annealed free organic solar cell and production method thereof |
| CN111247655A (en) * | 2017-10-23 | 2020-06-05 | 住友化学株式会社 | Photoelectric conversion element |
| CN110993791A (en) * | 2019-12-09 | 2020-04-10 | 东华大学 | Method for regulating and controlling growth of conductive polymer film crystal |
| CN112701225A (en) * | 2020-12-29 | 2021-04-23 | 深圳大学 | Stretchable photoelectric detector and preparation method thereof |
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