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首页> 外文期刊>Advanced Materials >Self-Assembled Monolayers of Cyclohexyl-Terminated Phosphonic Acids as a General Dielectric Surface for High-Performance Organic Thin-Film Transistors
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Self-Assembled Monolayers of Cyclohexyl-Terminated Phosphonic Acids as a General Dielectric Surface for High-Performance Organic Thin-Film Transistors

机译:环己基末端膦酸的自组装单分子层,作为高性能有机薄膜晶体管的通用介电表面

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摘要

Self-assembled monolayers (SAMs) provide a versatile molecular platform that can dramatically change the surface properties by varying the terminal groups. The cyclohexyl group is an unprecedented terminal group for all kinds of SAMs, to the best of our knowledge. Interestingly, cyclohexyl terminal groups are present in the phospholipid bilayers of acid- and heat-resistant bacteria (Bacillus acidocaldarius), and make a major contribution to the acid- and heat-tolerance of the cell membrane. Here, we report a novel cyclohexyl-terminated SAM from 12-cyclohexyldodecylphosphonic acid (CDPA in Figure 1a). The most important finding from this study is that molecules of CDPA self-assemble into a highly ordered molecular monolayer on AlO_y/TiO_x, a solution-processed high-k metal oxide, providing a general dielectric surface for high-performance organic thin-film transistors (OTFTs). The CDPA-modified AlO_y/TiO_x functions as an excellent dielectric enabling OTFTs with high field effect mobility of up to 5.7 cm~2 V~(-1) s~(-1) for holes and 5.5 cm~2 V~(-1) s~(-1) for electrons, good air stability with low operating voltage, and general applicability to solution-processed and vacuum-deposited p-type and n-type organic semiconductors.
机译:自组装单分子膜(SAMs)提供了一种通用的分子平台,该分子平台可以通过改变端基来显着改变表面性质。据我们所知,环己基是各种SAM的空前末端基团。有趣的是,环己基末端基团存在于耐酸和耐热细菌(酸性芽孢杆菌)的磷脂双层中,并且对细胞膜的耐酸和耐热性做出了重要贡献。在这里,我们从12-环己基十二烷基膦酸(图1a中的CDPA)报告了一种新型的以环己基封端的SAM。这项研究最重要的发现是CDPA分子在溶液处理的高k金属氧化物AlO_y / TiO_x上自组装成高度有序的分子单层,为高性能有机薄膜晶体管提供了通用的介电表面(OTFT)。 CDPA改性的AlO_y / TiO_x具有出色的介电性能,使OTFT的高场效应迁移率高达5.7 cm〜2 V〜(-1)s〜(-1),孔洞可达5.5 cm〜2 V〜(-1) )s〜(-1)用于电子,空气稳定性好,工作电压低,并且通常适用于溶液处理和真空沉积的p型和n型有机半导体。

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  • 来源
    《Advanced Materials》 |2014年第42期|7190-7196|共7页
  • 作者单位

    Department of Chemistry The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China;

    Department of Chemistry The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China;

    Department of Electronic Engineering The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China;

    Department of Chemical Engineering Stanford University Stanford, California 94305, USA;

    SLAC National Accelerator Laboratory Menlo Park, California 94025, USA;

    Department of Chemical Engineering Stanford University Stanford, California 94305, USA;

    Department of Electronic Engineering The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China;

    Department of Chemistry The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China,Center of Novel Functional Molecules The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China;

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