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Small-Molecule-Based Organic Photovoltaic Devices Covering Visible and Near-Infrared Absorption through Phase Transition of Titanylphthalocyanine Induced by Solvent Exposure

机译:小分子基有机光伏器件覆盖了通过溶剂暴露引起的钛酰酞菁的相变可见和近红外吸收

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摘要

Small-molecule p-n heterojunction organic photovoltaic (OPV) devices with a two-component donor layer composed of tetrabenzoporphyrin (BP) and titanyl phthalocyanine (TiOPc) can utilize near-infrared (NIR) light up to 950 nm and shows a 2.4% power conversion efficiency (PCE) (J_(sc) = 7.7mA/cm~2; open circuit voltage, V_∞ = 0.61 V; and fill factor, FF = 0.50) under AM1.5G illumination at an intensity of 100mW/cm~2. This value is higher than the 2.0% value obtained by an archetypal device composed of a single-component BP layer. The device performance was improved by the exposure of the TiOPc layer to toluene, which induced a rapid change in the morphology of the TiOPc layer from what is called Phase I to Phase II. The acceptor layer comprising 1,4-bis(dimethyl-phenylsilylrnethyl)[60]fullerene (SIMEF) showed higher V_(oc) and PCE than that comprising popular PCBM, because the lowest unoccupied molecular orbital (LUMO) level of SIMEF is higher than that of PCBM.
机译:具有由四苯并卟啉(BP)和钛氧基酞菁(TiOPc)组成的双组分供体层的小分子pn异质结有机光伏(OPV)器件可以利用高达950 nm的近红外(NIR)光,并显示2.4%的功率转换效率(PCE)(J_(sc)= 7.7mA / cm〜2;开路电压V_∞= 0.61 V;填充系数FF = 0.50)在AM1.5G照明下强度为100mW / cm〜2。该值高于由单组分BP层组成的原型设备获得的2.0%值。通过将TiOPc层暴露在甲苯中,可以改善器件性能,从而使TiOPc层的形态从所谓的I相快速转变为II相。包含1,4-双(二甲基-苯基甲硅烷基甲基)[60]富勒烯(SIMEF)的受主层比包含流行的PCBM的受主层具有更高的V_(oc)和PCE,因为SIMEF的最低未占用分子轨道(LUMO)水平高于PCBM。

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  • 来源
    《Japanese journal of applied physics》 |2011年第12期|p.121603.1-121603.4|共4页
  • 作者单位

    Department of Chemistry, The University of Tokyo, Bunkyo, Tokyo 113-0033, Japan,Mitsubishi Chemical Group Science and Technology Research Center, Inc., Yokohama 227-8502, Japan;

    Mitsubishi Chemical Group Science and Technology Research Center, Inc., Yokohama 227-8502, Japan;

    Department of Chemistry, The University of Tokyo, Bunkyo, Tokyo 113-0033, Japan;

    Department of Chemistry, The University of Tokyo, Bunkyo, Tokyo 113-0033, Japan;

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