用户名: 密码: 验证码:
Dithienocarbazole- and benzothiadiazole-based donor-acceptor conjugated polymers for bulk heterojunction polymer solar cells
详细信息    查看全文
  • 作者:Ziqing Rong ; Yunfeng Deng ; Zhiyuan Xie ; Yanhou Geng ; Fosong Wang
  • 关键词:conjugated polymer ; dithienocarbazole ; benzothiadiazole ; polymer solar cells ; power conversion efficiency
  • 刊名:SCIENCE CHINA Chemistry
  • 出版年:2015
  • 出版时间:February 2015
  • 年:2015
  • 卷:58
  • 期:2
  • 页码:294-300
  • 全文大小:1,063 KB
  • 参考文献:1. Cao WR, Xue JG. Recent progress in organic photovoltaics: device architecture and optical design. / Energy Environ Sci, 2014, 7: 2123-144 CrossRef
    2. Brabec CJ, Gowrisanker S, Halls JJM, Laird D, Jia SJ, Williams SP. Polymer-fullerene bulk-heterojunction solar cells. / Adv Mater, 2010, 22: 3839-856 CrossRef
    3. Li YF. Molecular design of photovoltaic materials for polymer solar cells: toward suitable electronic energy levels and broad absorption. / Acc Chem Res, 2012, 45: 723-33 CrossRef
    4. Li G, Zhu R, Yang Y. Polymer solar cells. / Nat Photonics, 2012, 6: 153-61 CrossRef
    5. Zhou HX, Yang LQ, You W. Rational design of high performance conjugated polymers for organic solar cells. / Macromolecules, 2012, 45: 607-32 CrossRef
    6. Zhang ZG, Wang JZ. Structures and properties of conjugated donor-acceptor copolymers for solar cell applications. / J Mater Chem, 2012, 22: 4178-187 CrossRef
    7. Cheng YJ, Yang SH, Hsu CS. Synthesis of conjugated polymers for organic solar cell applications. / Chem Rev, 2009, 109: 5868-923 CrossRef
    8. Günes S, Neugebauer H, Sariciftci NS. Conjugated polymer-based organic solar cells. / Chem Rev, 2007, 107: 1324-338 CrossRef
    9. Chao YH, Jheng JF, Wu JS, Wu KY, Peng HH, Tsai MC, Wang CL, Hsiao YN, Wang CL, Lin CY, Hsu CS. Porphyrin-incorporated 2D D-A polymers with over 8.5% polymer solar cell efficiency. / Adv Mater, 2014, 26: 5205-210 CrossRef
    10. Zhang MJ, Guo X, Ma W, Zhang SQ, Huo LJ, Ade H, Hou JH. An easy and effective method to modulate molecular energy level of the polymer based on benzodithiophene for the application in polymer solar cells. / Adv Mater, 2014, 26: 2089-095 CrossRef
    11. Yusoff ARM, Lee SJ, Kim HP, Shneider FK, Silva WJ, Jang J. 8.91% power conversion efficiency for polymer tandem solar cells. / Adv Funct Mater, 2014, 24: 2240-247 CrossRef
    12. Jiang JM, Lin HK, Lin YC, Chen HC, Lan SC, Chang CK, Wei KH. Side chain structure affects the photovoltaic performance of two-dimensional conjugated polymers. / Macromolecules, 2014, 47: 70-8 CrossRef
    13. Li K, Li ZJ, Feng K, Xu XP, Wang LY, Peng Q. Development of large band-gap conjugated copolymers for efficient regular single and tandem organic solar cells. / J Am Chem Soc, 2013, 135: 13549-3557 CrossRef
    14. Zhang MJ, Gu Y, Guo X, Liu F, Zhang SQ, Huo LJ, Russell TP, Hou JH. Efficient polymer solar cells based on benzothiadiazole and alkylphenyl substituted benzodithiophene with a power conversion efficiency over 8%. / Adv Mater, 2013, 25: 4944-949 CrossRef
    15. Wang N, Chen Z, Wei W, Jiang ZH. Fluorinated benzothiadiazole-based conjugated polymers for high-performance polymer solar cells without any processing additives or post-treatments. / J Am Chem Soc, 2013, 135: 17060-7068 CrossRef
    16. Guo XG, Zhou NJ, Lou SJ, Smith J, Tice DB, Hennek JW, Ortiz RP, Navarrete JTL, Li SY, Strzalka J, Chen LX, Chang RPH, Facchetti A, Marks TJ. Polymer solar cells with enhanced fill factors. / Nat Photonics, 2013, 7: 825-33 CrossRef
    17. Son HJ, Lu LY, Chen W, Xu T, Zheng TY, Carsten B, Strzalka J, Darling SB, Chen
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Chinese Library of Science
    Chemistry
  • 出版者:Science China Press, co-published with Springer
  • ISSN:1869-1870
文摘
Donor-acceptor (D-A)-conjugated polymers P(BT-C1) and P(BT-C2), with dithieno[2,3-b;7,6-b]carbazole (C1) or dithieno[ 3,2-b;6,7-b]carbazole (C2) as D-unit and benzothiadiazole (BT) as A-unit, were synthesized. The optical bandgaps of the polymers are similar (1.84 and 1.88 eV, respectively). The structures of donor units noticeably influence the energy levels and backbone curvature of the polymers. P(BT-C1) shows a large backbone curvature; its highest occupied molecular orbital (HOMO) energy level is ?.18 eV, whereas P(BT-C2) displays a pseudo-straight backbone and has a HOMO energy level of ?.37 eV. The hole mobilities of the polymers without thermal annealing are 1.9×10? and 2.7×10? cm2V?s? for P(BT-C1) and P(BT-C2), respectively, as measured by organic thin-film transistors (OTFTs). Polymer solar cells using P(BT-C1) and P(BT-C2) as the donor and phenyl-C71-butyric acid methyl ester (PC71BM) as the acceptor were fabricated. Power conversion efficiencies (PCEs) of 4.9% and 5.0% were achieved for P(BT-C1) and P(BT-C2), respectively. The devices based on P(BT-C2) exhibited a higher V oc due to the deeper HOMO level of the polymer, which led to a slightly higher PCE.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700