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Solution-Processable Low-Molecular Weight Extended Arylacetylenes: Versatile p-Type Semiconductors for Field-Effect Transistors and Bulk Heterojunction Solar Cells

机译:溶液可加工的低分子量扩展芳基乙炔:场效应晶体管和大容量异质结太阳能电池的多功能p型半导体

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摘要

We report the synthesis and characterization of a series of five extended arylacetylenes, 9,10-bis-{[m,p-bis(hexyloxy)phenyl]ethynyl}-anthracene (A-P6t, 1), 9,10-bis-[(p-{[m,p-bis(hexyloxy) phenyl]ethynyl} phenyl)ethynyl]-anthracene (PA-P6t, 2), 4,7-bis-{[m,p-bis(hexyloxy)phenyl]ethynyl}-2,1,3-benzothiadiazole (BTZ-P6t, 5), 4,7-bis(5-{[m,p-bis(hexyloxy)phenyl]ethynyl}thien-2-yl)-2,1,3-benzothiadiazole (TBTZ-P6t, 6), and 7,7'-({[m,p-bis(hexyloxy)phenyl]ethynyl}-2,1,3-benzothiadiazol-4,4'-ethynyl)-2,5-thiophene (BTZT-P6t, 7), and two arylvinylenes, 9,10-bis-{(E)-[m,p-bis(hexyloxy)phenyl]vinyl}-anthracene (A-P6d, 3), 9,10-bis-[(E)-(p-{(E)-[m,p-bis(hexyloxy)phenyl]vinyl}phenyl)vinyl]-anthracene (PA-P6d, 4). Trends in optical absorption spectra and electrochemical redox processes are first described. Next, the thin-film microstructures and morphologies of films deposited from solution under various conditions are investigated, and organic field-effect transistors (OFETs) and bulk heterojunction photovoltaic (OPV) cells fabricated. We find that substituting acetylenic for olefinic linkers on the molecular cores significantly enhances device performance. OFET measurements reveal that all seven of the semiconductors are FET-active and, depending on the backbone architecture, the arylacetylenes exhibit good p-type mobilities (μ up to ~0.1 cm~2 V~(-1) s~(-1)) when optimum film microstructural order is achieved. OPV cells using [6,6]-phenyl C_(61)-butyric acid methyl ester (PCBM) as the electron acceptor exhibit power conversion efficiencies (PCEs) up to 1.3% under a simulated AM 1.5 solar irradiation of 100 mW/cm~2. These results demonstrate that arylacetylenes are promising hole-transport materials for p-channel OFETs and promising donors for organic solar cells applications. A direct correlation between OFET arylacetylene hole mobility and OPV performance is identified and analyzed.
机译:我们报告了一系列五个扩展的芳基乙炔,9,10-双-{[m,对-双(己氧基氧基)苯基]乙炔基}-蒽(A-P6t,1),9,10-双- [(对-{[m,对-双(己氧基氧基)苯基]乙炔基}苯基)乙炔基]-蒽(PA-P6t,2),4,7-双-{[m,对-双(己氧基氧基)苯基]乙炔基} -2,1,3-苯并噻二唑(BTZ-P6t,5),4,7-双(5-{[m,p-双(己氧基氧基)苯基]乙炔基} thien-2-yl)-2,1 ,3-苯并噻二唑(TBTZ-P6t,6)和7,7'-({[m,p-双(己氧基氧基)苯基]乙炔基} -2,1,3-苯并噻二唑-4,4'-乙炔基)- 2,5-噻吩(BTZT-P6t,7)和两个芳基乙烯基,9,10-双-{(E)-[m,对-双(己氧基)苯基]乙烯基}-蒽(A-P6d,3) ,9,10-双-[(E)-(对-{(E)-[m,对-双(己氧基氧基)苯基]乙烯基}苯基)乙烯基]蒽(PA-P6d,4)。首先描述了光吸收光谱和电化学氧化还原过程的趋势。接下来,研究了在各种条件下从溶液中沉积的薄膜的薄膜微结构和形态,并制造了有机场效应晶体管(OFET)和体异质结光伏(OPV)电池。我们发现,在分子核上用炔烃取代烯烃连接基可显着提高器件性能。 OFET测量表明,所有七个半导体均具有FET活性,并且取决于主链结构,芳基乙炔具有良好的p型迁移率(μ高达〜0.1 cm〜2 V〜(-1)s〜(-1) )当达到最佳的薄膜微结构顺序时。使用[6,6]-苯基C_(61)-丁酸甲酯(PCBM)作为电子受体的OPV电池在100 mW / cm〜的模拟AM 1.5太阳辐射下显示出高达1.3%的功率转换效率(PCE)。 2。这些结果证明,芳基乙炔是用于p沟道OFET的有希望的空穴传输材料,并且是有机太阳能电池应用的有希望的供体。确定并分析了OFET芳基乙炔空穴迁移率与OPV性能之间的直接关系。

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  • 来源
    《Journal of the American Chemical Society》 |2010年第17期|P.6108-6123|共16页
  • 作者单位

    Department of Chemistry, the Argonne-Northwestern Solar Energy Research Center, and the Materials Research Center, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113 ETH Zuerich, Laboratory of Organic Chemistry, Department of Chemistry and Applied Biosciences, HCI G 304 Wolfgang-Pauli-Strasse 10, CH-8093 Zuerich, Switzerland;

    rnDepartment of Chemistry, University of Perugia, Via Elce di Sotto 8, 1-06123 Perugia, Italy;

    rnDepartment of Chemistry, University of Perugia, Via Elce di Sotto 8, 1-06123 Perugia, Italy;

    rnDepartment of Chemistry, the Argonne-Northwestern Solar Energy Research Center, and the Materials Research Center, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113;

    rnDepartment of Chemistry, the Argonne-Northwestern Solar Energy Research Center, and the Materials Research Center, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113;

    rnDepartment of Chemistry, the Argonne-Northwestern Solar Energy Research Center, and the Materials Research Center, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113;

    rnDepartment of Chemistry, University of Perugia, Via Elce di Sotto 8, 1-06123 Perugia, Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:15:34

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