SELF DOPING MATERIALS AND METHODS
    2.
    发明申请
    SELF DOPING MATERIALS AND METHODS 审中-公开
    自制材料与方法

    公开(公告)号:US20150243869A1

    公开(公告)日:2015-08-27

    申请号:US14626695

    申请日:2015-02-19

    CPC classification number: H01L35/24 C07D471/06

    Abstract: A an organic material is shown including a conjugated core, one or more electron donating moieties, and a non-conjugated spacer coupled between the conjugated core and the electron donating moiety. Methods of forming the organic material include solution based processing. One example of an organic material includes a self-doping n-type organic material.

    Abstract translation: 显示了一种有机材料,其包括共轭核心,一个或多个给电子部分和偶联在共轭核心和给电子部分之间的非共轭间隔基。 形成有机材料的方法包括基于溶液的处理。 有机材料的一个实例包括自掺杂n型有机材料。

    N-TYPE DOPANTS FOR EFFICIENT SOLAR CELLS

    公开(公告)号:US20220293866A1

    公开(公告)日:2022-09-15

    申请号:US17826455

    申请日:2022-05-27

    Abstract: Triazabicylodecene can effectively n-dope a variety of organic semiconductors, including PCBM, thus increasing in-plane conductivities. We synthesized a series of TBD-based n-dopants via an N-alkylation reaction and studied the effect of various alkyl chains on the physical and device properties of the dopants. Combining two TBD moieties on a long alky chain gave a solid dopant, 2TBD-C10, with high thermal stability above 250° C. PCBM films doped by 2TBD-C10 were the most tolerant to thermal annealing and reached in-plane conductivities of 6.5×10−2 S/cm. Furthermore, incorporating 2TBD-C10 doped PCBM as the electron transport layer (ETL) in methylammonium lead triiodide (MAPbI3) based photovoltaics led to a 23% increase in performance, from 11.8% to 14.5% PCE.

    MODULAR STRATEGY FOR INTRODUCING END-GROUP FUNCTIONALITY INTO CONJUGATED COPOLYMERS
    9.
    发明申请
    MODULAR STRATEGY FOR INTRODUCING END-GROUP FUNCTIONALITY INTO CONJUGATED COPOLYMERS 审中-公开
    将端基功能引入共轭共聚物的模块化策略

    公开(公告)号:US20130248833A1

    公开(公告)日:2013-09-26

    申请号:US13850040

    申请日:2013-03-25

    Abstract: The invention provides methods for making and using end-functionalized conjugated polymers. Embodiments of the invention comprise performing a coupling polymerization in the presence of AA monomers, BB monomers and an end capping compound that can react with a monomer and which is selected to include a functional group. The functional end groups can, for example, comprise polymers or small molecules selected for their ability to produce conjugated polymers that self-assemble into thermodynamically ordered structures. In certain embodiments of the invention, nano-scale morphology of such conjugated polymer compositions can be driven by the phase separation of two covalently bound polymer blocks. These features make the use of conjugated polymers an appealing strategy for exerting control over active layer morphology in semiconducting polymer materials systems.

    Abstract translation: 本发明提供了制备和使用端官能化共轭聚合物的方法。 本发明的实施方案包括在AA单体,BB单体和可与单体反应并且被选择为包括官能团的封端化合物的存在下进行偶联聚合。 功能性端基可以例如包含聚合物或小分子,这些聚合物或小分子被选择用于产生自组装成热力学有序结构的共轭聚合物的能力。 在本发明的某些实施方案中,这种共轭聚合物组合物的纳米级形态可以通过两个共价结合的聚合物嵌段的相分离来驱动。 这些特征使共轭聚合物成为在半导体聚合物材料体系中对活性层形态进行控制的有吸引力的策略。

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