PUKYONG

고분자 태양전지를 위한 새로운 공액 고분자의 합성 및 태양전지 특성 평가

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Abstract
Polymer solar cells have great potential for flexible polymeric electronic device because of their cost effective and light weight. The bulk heterojunction (BHJ) layers exhibit nanoscale mixing of the two components ensuring quantitative charge generation at the extended donor?acceptor interface whereas the bicontinuous nature allows effective charge collection. Low band gap energy is crucial factor for making efficient solar cell. To get low bad gap polymer, we introduced electron deficient anthraquinone derivative and electron rich dialkoxy benzene derivatives. The polymers are synthesized by the well-known Heck coupling reaction. The polymers based on anthraquinone and dialkoxy benzene have low band gap. ca. 2.10 eV. However, the efficiency of solar cell based the polymers are extremely low because the carbonyl group in the back-bone seem to be act as an exciton quenching site. In addition, we synthesized a series of low band gap polymers based dihexylfluorene, 2,1,3-benzothiadiazole, and dialkoxythiophene by the Suzuki coupling reaction. The efficiency of solar cells based on the low band gap polymers are ca. 0.3%. In this thesis, we report the synthesis and characterization of new polymer. The electrochemical, optical, photovoltaic properties of new polymers as well.
Author(s)
박상준
Issued Date
2011
Awarded Date
2011. 2
Type
Dissertation
Publisher
부경대학교
URI
https://repository.pknu.ac.kr:8443/handle/2021.oak/9629
http://pknu.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000001963885
Department
대학원 고분자공학과
Advisor
김주현
Table Of Contents
Chapter Ⅰ. Introduction 1
Ⅰ-1. 유기태양전지의 연구배경 및 소개 1
Ⅰ-2. 유기태양전지의 기본 구조 4
Ⅰ-3. 유기태양전지의 개발과정 8
Ⅰ-4. 유기태양전지와 관련된 이론 및 설명 9
Ⅰ-4-1. 전도성 고분자의 정의 및 특성 9
Ⅰ-4-2. AM 1.5 (Air Mass 1.5) 10
Ⅰ-4-3. 밴드 갭 12
Ⅰ-4-4. 개방 전압 (Open circuit voltage, Voc) 14
Ⅰ-4-5. 단락 전류(Short circuit current, Jsc) 14
Ⅰ-4-6. Fill factor (FF) 15
Ⅰ-4-7. 변환 효율 (power conversion efficiency, PCE,η) 15
Ⅰ-4-8. 형광(photoluminascence)과 quenching 효과 18
Ⅰ-5. 유기태양전지의 구동 원리 20
Ⅰ-5-1. 빛의 흡수 (Light absorption) 20
Ⅰ-5-2. 전자-정공의 분리 (charge separation) 21
Ⅰ-5-3. 전하의 수집 (Collection of photo-charge carriers) 22
Chapter Ⅱ. Anthraquinone를 기본으로 하는 공액 이중결합 고분자들의 합성 및 전기 광학 특성 평가 24
Ⅱ-1. 서 론 24
Ⅱ-2. 실 험 25
Ⅱ-2-1. 단량체의 합성 25
Ⅱ-2-1-1. 2,6-Diiodo-anthraquinone의 합성(1) 25
Ⅱ-2-1-2. 2-(10-Dicyanomethylene-2,6-diiodo-10H-anthracen- -9-ylidene)-malononitrile의 합성(2) 26
Ⅱ-2-1-3. 1,4-Bis(dodecyloxy)-2,5-divinylbenzene의 합성(3) 26
Ⅱ-2-2. 중합 27
Ⅱ-2-2-1. PAQ (poly-2-[2-(2,5-bis-dodecyloxy-4-vinyl-phenyl)-vinyl]-anthraquinone)의 합성(4) 27
Ⅱ-2-2-2. PAN4CN(poly-2-{2-[2-(2,5-bis-dodecyloxy-4-vinyl-phenyl)-vinyl]-10dicyanomethylene-10H-anthracen -9-ylidene}-malononitrile)의 합성(5) 28
Ⅱ-2-3. 측정 29
Ⅱ-3. 결과 및 고찰 29
Ⅱ-4. 결 론 36
Chapter Ⅲ. 유기태양전지에 적용 가능한 3,4-dialkoxythiophene, 2,1,3-benzothiadiazole, and 9,9,-dialkylfluorene를 기본으로 하는 저 밴드 갭을 가지는 고분자들의 합성 및 전기 광학적 특성 평가 37
Ⅲ-1. 서 론 37
Ⅲ-2. 실 험 38
Ⅲ-2-1. 단량체의 합성 38
Ⅲ-2-1-1. Ethoxycarbonylmethylsulfanyl-acetic acid ethyl ester의 합성 (1) 39
Ⅲ-2-1-2. 3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid di-ethyl ester의 합성(2) 39
Ⅲ-2-1-3. 3, 4-Ethylenedioxythiophene(EDOT)의 합성(3) 40
Ⅲ-2-1-4. 2-Tributylstannyl-3,4-ethylenedioxythiophene의 합성(4) 41
Ⅲ-2-1-5. 4,7-Dibromo-benzo[2,1,3]thiadiazole의 합성(5) 41
Ⅲ-2-1-6. 4-Bromo-7-(7-bromo-2,3-dihydro-thieno[3,4-b] [1,4]-dioxin-5-yl)-benzo[2,1,3]thiadiazole의 합성(6) 42
Ⅲ-2-1-7. 4,7-Bis-(7-bromo-2,3-dihydro-thieno[3,4-b][1,-4] dioxin-5-yl)-benzo[2,1,3]thiadiazole의 합성(7) 42
Ⅲ-2-1-8. 2,7-bis(4,4,5,5-tetramethyl-[1,3,2]dioxaborolane)-9,9-dihexyl-9H-fluoren-2-yl(8)의 합성 43
Ⅲ-2-2. 중합 44
Ⅲ-2-2-1. poly[4-[7-(9,9-Dihexyl-9H-fluoren-2-yl)-2,3-di--hydro-thieno[3,4-b][1,4]dioxin-5-yl]-7-(2,3-dihydro thieno[3,4-b][1,4]dioxin-5-yl)-benzo[2,1,3]thiadiazole] (PDHFTBT)의 중합 44
Ⅲ-2-2-2. poly[4-(9,9-Dihexyl-9H-fluoren-2-yl)-7-(2,3-di--hydro-thieno[3,4-b][1,4]dioxin-5-yl)-benzo[2,1,3] thiadiazole](PDHFBT)의 중합 44
Ⅲ-2-3. 측정 47
Ⅲ-2-4. 유기태양전지의 제작 48
Ⅲ-3. 결과 및 고찰 48
Ⅲ-4. 결 론 59
References 60
Degree
Master
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