유기태양전지의 효율 향상을 위한 새로운 고분자의 합성 및 광전변환특성에 대한 연구
- Alternative Title
- Synthesis and photovoltaic properties of new π-conjugated polymers for improvement of efficiency in organic photovoltaic cells.
- Abstract
- π-conjugated polymer based bulk hetero-junction (BHJ) solar cells have been attracting considerable attention recently due to their unique advantage of low cost, light weight and potential application in flexible large-area devices. The BHJ of π-conjugated polymers (electron donor) blended with fullerene (C60) derivatives (electron
acceptor) should boost the efficiency of polymer solar cells. Power conversion efficiency (PCE) up to 5% has been obtained from both the BHJ solar cells of poly(3-hexylthiophene) (P3HT) blended with (6)-1-(3-(methoxycarbonyl)propyl)-{5}-1-1-phenyl-[5,6]-fullerene (PCBM) and one of poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4b]-dithiophene)-alt-4,7-benzo(2,1,3)thiadiazole)](PCPDTBT) blended with PCBM. The BHJ solar cells made from P3HT and PCPDTBT had high fill factor (FF) and short circuit current density (Jsc), while PCE was still limited by 0.60 ~ 0.65 V of lower open circuit voltage (Voc). The mean of increasing Voc is a facile method to improve PCE. Recently, the BHJ polymer solar cell using 4,7-dithiophen-2-yl-benzo(1,2,5)thiadiazole based alternating copolymers such as PFDTBT have demonstrated larger Voc (0.95 ~ 1.04 V), however, their PCE is still low owing to the lower Jsc than that of both P3HT and PCPDTBT based cells. If the Jsc of this type of copolymer based solar cells can be further enhanced while
maintaining their large Voc, higher PCE can be expected. Poly[4,7-dithiophen-2-ylbenzo(1,2,5)thiadiazole-alt-1,4-bis(dodecyloxy)-2,5-divinylbenzene] (PPVTBT) and poly[4,7-dithiophene-2-yl-benzo(1,2,5)thiadiazole-alt-dihexyl-9H-fluorene] (PFTBT) based on 4,7-dithiophene-2-yl-benzo(1,2,5)thiadiazole were synthesized using Heck and Suzuki coupling reactions. Poly[2,3-dimethyl-5,8-dithiophene-2-yl-quinoxaline-alt-9,9-dihexyl-9H-fluorene] (PFTQT) and poly[2,3-dimethyl-5,8-dithiophen-2-yl-quinoxaline-alt-10-hexyl-10H-phenothiazine] (PPTTQT) based on 2,3-dimethyl-5,8-dithiophen-2-yl-quinoxaline were synthesized using Suzuki coupling reaction. All polymers were soluble in common organic solvents such as chloroform, chlorobenzene, dichlorobenzene, THF and
toluene. The band gap of polymers were estimated UV-Vis spectroscopy and cyclic voltammogram between 1.7 ~ 2.3 eV. The BHJ type photovoltaic cells were fabricated with polymer and PCBM [ITO/PEDOT:PSS/polymer:PCBM/Al]. New polymers were showed broad absorption regions and had proper energy levels. The BHJ type photovoltaic cells were expected to high Jsc and PCE due to the good overlap of solar energy.
- Author(s)
- 신웅
- Issued Date
- 2010
- Awarded Date
- 2010. 2
- Type
- Dissertation
- Keyword
- organic photovoltaic cell solar cell electron donor low band gap
- Publisher
- 부경대학교
- URI
- https://repository.pknu.ac.kr:8443/handle/2021.oak/11754
http://pknu.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000001955928
- Alternative Author(s)
- Woong Shin
- Affiliation
- 부경대학교 일반대학원
- Department
- 대학원 청정화학공학부고분자공학전공
- Advisor
- 김주현
- Table Of Contents
- Contents
List of Figures
List of Tables
List of Schemes
Abstract
Chapter Ⅰ. Introduction
Ⅰ-1. Solar energy for future clean energy
Ⅰ-2. Experimental histories of organic photovoltaic cells
Ⅰ-3. Basic concept of organic photovoltaic cells
Ⅰ-3-1. Operating process of bulk hetero-junction photovoltaic cells
Ⅰ-3-2. Photon to current conversion steps of organic photovoltaic cells
1. Absorption of photons
2. Exciton diffusion
3. Charge separation
4. Charge transport
5. Charge collection
Ⅰ-3-3. General structures of organic photovoltaic cells
Ⅰ-3-4. Kinds of electron donor and acceptor materials
Ⅰ-4. The theory of organic photovoltaics
Ⅰ-4-1. Conducting polymers
1. Band theory
2. Free electron theory
3. Properties
4. Applications
Ⅰ-4-2. Fluorescence and phosphorescence
Ⅰ-4-3. Open circuit voltage (Voc)
Ⅰ-4-4. Short circuit current (Jsc, Isc)
Ⅰ-4-5. Fill factor (FF)
Ⅰ-4-6. Power conversion efficiency (PCE, η)
Ⅰ-4-7. Photo-induced charge transfer (PICT)
Ⅰ-4-8. Air mass (AM)
Ⅰ-4-9. Luminescence and quenching effect
Ⅰ-5. Variety of solar cells
Ⅰ-5-1. Silicon based inorganic solar cells
1. Crystalline silicon cells
2. Amorphous silicon cells
Ⅰ-5-2. CdTe solar cells
Ⅰ-5-3. CIGS (CuInGaSe2) solar cells
Ⅰ-5-4. Bulk hetero-junction solar cells
Ⅰ-5-5. Dye-sensitized solar cells (DSSC)
Ⅰ-6. The comparison of inorganic and organic solar cells
Chapter Ⅱ. Synthesis and photovoltaic properties of low band gap polymers based on 4,7-dithiophen-2-yl-benzo(1,2,5)thiadiazole
Ⅱ-1. Introduction
Ⅱ-2. Measuring equipments and fabrication of device
Ⅱ-2-1. Measurement
1. Structural analysis
2. Physical analysis
3. Optical and electrochemical analysis
4. Photovoltaic analysis
Ⅱ-2-2. Fabrication of organic photovoltaic device
Ⅱ-3. Reagents and Synthesis
Ⅱ-3-1. Reagents and solvents
Ⅱ-3-2. Synthesis of monomers and polymers
Ⅱ-3-2-1. Synthesis of 4,7-dibromo-benzo(1,2,5)thiadiazole(1)
Ⅱ-3-2-2. Synthesis of 4,4,5,5-tetramethyl-2-thiophen-2-yl-[1,3,2]dioxaborolane(2)
Ⅱ-3-2-3. Synthesis of 4,7-dithiophen-2-yl-benzo(1,2,5)thiadiazole(3)
Ⅱ-3-2-4. Synthesis of 4,7-bis(5-bromo-thiophen-2-yl)-benzo(1,2,5)thiadiazole(4)
Ⅱ-3-2-5. Synthesis of 1,4-bis(dodecyloxy)-2,5-divinylbenzene(5)
Ⅱ-3-2-6. Synthesis of 2,7-bis(4,4,5,5-tetramethyl-[1,3,2]dioxaborolane)-9,9-dihexyl-9H-fluoren-2-yl(6)
Ⅱ-3-2-7. Polymerization of poly[4,7-dithiophen-2-yl-benzo(1,2,5)thiadiazole-alt-1,4-bis(dodecyloxy)-2,5-divinylbenzene] (PPVTBT)
Ⅱ-3-2-8. Polymerization of poly[4,7-dithiophen-2-yl-benzo(1,2,5)thiadiazole]-alt-9,9-dihexyl-9H-fluorene] (PFTBT)
Ⅱ-4. Results and discussion
Ⅱ-5. Conclusion
Chapter Ⅲ. Synthesis and photovoltaic properties of polymers based on 2,3-dimethyl-5,8-dithiophen-2-yl-quinoxaline
Ⅲ-1. Introduction
Ⅲ-2. Reagents and Synthesis
Ⅲ-3-1. Reagents and solvents
Ⅲ-3-2. Synthesis of monomers and polymers
Ⅲ-2-2-1. Synthesis of 3,6-dibromo-1,2-phenylenediamine(1)
Ⅲ-2-2-2. Synthesis of 5,8-dibromo-2,3-dimethyl-quinoxaline(2)
Ⅲ-2-2-3. Synthesis of 4,4,5,5-tetramethyl-2-thiophen-2-yl-[1,3,2]dioxaborolane(3)
Ⅲ-2-2-4. Synthesis of 2,3-dimethyl-5,8-dithiophen-2-yl-quinoxaline(4)
Ⅲ-2-2-5. Synthesis of 5,8-bis(5-bromo-thiophen-2-yl)-2,3-dimethyl-quinoxaline(5)
Ⅲ-2-2-6. Synthesis of 10-hexyl-3,7-bis(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-10H-phenothiazine(6)
Ⅲ-2-2-7. Synthesis of 2,7-bis(4,4,5,5-tetramethyl-[1,3,2]dioxaborolane)-9,9-dihexyl-9H-fluoren-2-yl(7)
Ⅲ-2-2-8. Polymerization of poly[2,3-dimethyl-5,8-dithiophen-2-ylquinoxaline-alt-9,9-dihexyl-9,9-dihexyl-9H-fluorene] (PFTQT)
Ⅲ-2-2-9. Polymerization of poly[2,3-dimethyl-5,8-
dithiophen-2-ylquinoxaline-alt-10-hexyl-10H-phenothiazine] (PPTTQT)
Ⅲ-3. Results and discussion
Ⅲ-4. Conclusion
References
- Degree
- Master
-
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