PUKYONG

편편하고 강직한 구조를 기본으로 한 새로운 공액고분자의 합성 및 광전변환특성에 대한 연구

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Alternative Title
Synthesis of flat and rigid structured polymers organic solar cells and their photovoltaic properties
Abstract
Regioregular poly(3-hexylthiophene) (P3HT) has been proven to be one of the successful electron donors for polymer bulk heterojunction (BHJ) solar cells. The regioregularity of P3HT plays an important role in the performance of solar cells because the regularity strongly associate with the morphology of thin film. The spectral overlap of the polymer with solar spectrum is also important factor for solar cell performance. To better match the solar spectrum, low-band gap polymers have been synthesized for polymer solar cells; however very few of them give a power conversion efficiency (PCE) of more than 5%. The low efficiency is probably due to the nonplanar structure of the polymer, which is detrimental for the close packing of polymer chains in the solid state. Here, we demonstrate a strategy for designing planar polymers with better chain packing in film to facilitate charge carrier transport for photovoltaic application.
The π-conjugated polymers with low-band gap based on 2,7-dibromofluorenone and 2-(2,7-dibromo-fluoren-9-ylidene)-malononitrile were synthesized by the Heck coupling and Suzuki coupling reactions. Also, we synthesized a series of low band gap polymers with very planar geometry based dialkoxyphenanthrene, 2,1,3-benzothiadiazole and thiophene by the Suziki coupling and Stille coupling reaction. All polymers were soluble in common organic solvents such as chloroform, chlorobenzene, dichlorobenzene and toluene. The band gap of polymers were estimated UV-Vis spectroscopy and cyclic voltammogram between 1.7 ~ 2.6 eV. The BHJ type photovoltaic cells were fabricated with polymer and PCBM ([6,6]-phenyl-C61-butyric
acid methyl ester). The efficieny of solar cells based on the low band gap polymers are ca. 0.1 ~ 0.2%. In this thesis, we report the synthesis and characterization of new polymer.
Author(s)
박정배
Issued Date
2011
Awarded Date
2011. 2
Type
Dissertation
Keyword
organic solar cell 전자주개 donor
Publisher
부경대학교
URI
https://repository.pknu.ac.kr:8443/handle/2021.oak/9867
http://pknu.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000001964128
Alternative Author(s)
Park, Jeong Bae
Affiliation
부경대학교 일반대학원
Department
대학원 고분자공학과
Advisor
김주현
Table Of Contents
Chapter Ⅰ. 서론 1
Ⅰ-1. 태양전지의 이해 1
Ⅰ-2. 유기태양전지의 구조 4
Ⅰ-3. 유기 태양전지의 기본 이론 7
Ⅰ-3-1. 전자주개(Electron donor)물질 7
Ⅰ-3-2. 전자받개(Electron acceptor)물질 7
Ⅰ-3-3. AM(Air mass) 1.5 8
Ⅰ-3-4. 빛 흡수(Light Absorption) & 엑시톤 생성(Exciton Generation) 7
Ⅰ-3-5. 엑시톤 확산(Exciton Diffusion) & 분리(Dissociation) 12
Ⅰ-3-6. Bilayer 형 15
Ⅰ-3-7. Bulk heterojunction 형 15
Ⅰ-3-8. 개방전압(Voc) 17
Ⅰ-3-9. 단락전류(JSC) 17
Ⅰ-3-10. 충진인자(FF) 17
Ⅰ-3-11. 변환효율(PCE, η) 18
Chapter Ⅱ. Synthesis and electro-optical properties of π-conjugated polymers based on 2-fluoren-9-ylidene-malononitrile 20
Ⅱ-1. 서론 20
Ⅱ-2. 실험 21
Ⅱ-2-1. 측정 22
Ⅱ-2-2. 단량체 및 고분자 합성 22
Ⅱ-2-3. 2-(2,7-Dibromo-fluoren-9-ylidene)-malononitrile의 합성 22
Ⅱ-2-4. 1,4-Bis(dodecyloxy)-2,5-divinylbenzene의 합성 23
Ⅱ-2-5. 2,7-Bis-(3-hexyl-thiophen-2-yl)-fluoren-9-one의 합성 23
Ⅱ-2-6. 2,7-Bis-(5-bromo-3-hexyl-thiophen-2-yl)-fluoren-9-one 의 합성 24
Ⅱ-2-7. 2-[2,7-Bis-(5-bromo-3-hexyl-thiophen-2-yl)-fluoren-9-ylid ene]-malononitrile의 합성 24
Ⅱ-2-8. 2,7-Bis(4,4,5,5-tetramethyl-[1,3,2]dioxaborolane)-9,9-dihexyl-9H-fluoren-2-yl의 합성 25
Ⅱ-2-9. Poly{2-[2-(2,5-bis-dodecyloxy-4-propenyl-phenyl)-vinyl]-7-methyl-fluoren-9-one} (PFone)의 중합 28
Ⅱ-2-10. Poly{2-[2-(2,5-bis-dodecyloxy-4-propenyl-phenyl)-vinyl]-7-methyl-fluoren-9-ylidene}-malononitrile (PF2CN)의 중합 28
Ⅱ-2-11. Poly{2-[5-(9,9-dihexyl-9H-fluoren-2-yl)-3-hexyl-thiophen-2-yl]-7-(3-hexyl-thiophen-2-yl)}-fluoren-9-one (PF-TFT)의 중합 29
Ⅱ-2-12. Poly{2-[2-[5-(9,9-dihexyl-9H-fluoren-2-yl)-3-hexyl-thiophen-2-yl]-7-(3-hexyl-thiophen-2-yl)-fluoren-9-ylidene]-malononitrile(PF-TCNT)의 중합 29
Ⅱ-3. 결과 및 고찰 31
Ⅱ-4. 결론 41
Chapter Ⅲ. Synthesis and Photovoltaic properties of copolymers based on 4,7-Di-thiophen-2-yl-benzo[2,1,3]thiadiazole and 9,10-dialkoxyph enanthrene 42
Ⅲ-1. 서론 42
Ⅲ-2. 실험 43
Ⅲ-2-1. 단량체 및 고분자 합성 43
Ⅲ-2-2-1. 4,7-Dibromo-benzo(2,1,3)thiadiazole의 합성 43
Ⅲ-2-2-2. 4,4,5,5-Tetramethyl-2-thiophen-2-yl-[1,3,2]dioxaborolane 44
Ⅲ-2-2-3. 4,7-Dithiophen-2-yl-benzo(2,1,3)thiadiazole의 합성 44
Ⅲ-2-2-4. 4,7-Bis(5-bromo-thiophen-2-yl)-benzo(2,1,3)thiadiazole의 합성 45
Ⅲ-2-2-5. Phenanthrene-9,10-dione의 합성 45
Ⅲ-2-2-6. 2,7-Dibromo-phenanthrene-9,10-dione의 합성 46
Ⅲ-2-2-7. 2,7-Dibromo-9,10-bis-decyloxy-phenanthrene의 합성 46
Ⅲ-2-2-8. 2,7-Dibromo-9,10-bis-dodecyloxy- phenanthrene의 합성 47
Ⅲ-2-2-9. 2,7-(9,10-Bis-decyloxy-phenanthren-2-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane의 합성 48
Ⅲ-2-2-10. 2,7-(9,10-Bis-dodecyloxy-phenanthren-2-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane의 합성 49
Ⅲ-2-2-11. Poly[4,7-dithiophen-2yl-benzo(1,2,5)thiadiazole]-alt-9,10-bis-decyloxy-phenanthrene]의 중합(PN10TBT-co) 49
Ⅲ-2-2-12. Poly[4,7-dithiophen-2yl-benzo(1,2,5)thiadiazole]-co-9,10-bis-decyloxy-phenanthrene]의 중합(PN10TBT-ter) 41
Ⅲ-2-2-13. Poly[4,7-dithiophen-2yl-benzo(1,2,5)thiadiazole]-alt-9,10-bis-dodecyloxy-phenanthrene]의 중합(PN12TBT-co) 50
Ⅲ-2-2-14. Poly[4,7-dithiophen-2yl-benzo(1,2,5)thiadiazole]-co-9,10-bis-dodecyloxy-phenanthrene]의 중합(PN12TBT-ter) 51
Ⅲ-2-2-15. Poly 4-{5-[7-(9,10-bis-dodecyloxy-phenanthren-2-yl)-9,9-bis-decyl-9H-fluoren-2-yl]-co-thiophen-2-yl}-7-thiophen-2-yl-benzo[1,2,5]thiadiazole의 중합(PFTBTPN5) 51
Ⅲ-3. 결과 및 고찰 54
Ⅲ-3. 결론 69
References 70
Degree
Master
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