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首页> 外文期刊>Advanced Functional Materials >Cooperative Effect of GO and Glucose on PEDOT:PSS for High V-OC and Hysteresis-Free Solution-Processed Perovskite Solar Cells
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Cooperative Effect of GO and Glucose on PEDOT:PSS for High V-OC and Hysteresis-Free Solution-Processed Perovskite Solar Cells

机译:GO和葡萄糖对PEDOT:PSS的协同作用,用于高V-OC和无滞后溶液处理的钙钛矿太阳能电池

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摘要

Hybrid organic-inorganic halide perovskites have emerged at the forefront of solution-processable photovoltaic devices. Being the perovskite precursor mixture a complex equilibrium of species, it is very difficult to predict/control their interactions with different substrates, thus the final film properties and device performances. Here the wettability of CH3NH3PbI3 (MAPbI(3)) onto poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) hole transporting layer is improved by exploiting the cooperative effect of graphene oxide (GO) and glucose inclusion. The glucose, in addition, triggers the reduction of GO, enhancing the conductivity of the PEDOT:PSS+GO+glucose based nanocomposite. The relevance of this approach toward photovoltaic applications is demonstrated by fabricating a hysteresis-free MAPbI(3) solar cells displaying a approximate to 37% improvement in power conversion efficiency if compared to a device grown onto pristine PEDOT:PSS. Most importantly, V-OC reaches values over 1.05 V that are among the highest ever reported for PEDOT:PSS p-i-n device architecture, suggesting minimal recombination losses, high hole-selectivity, and reduced trap density at the PEDOT:PSS along with optimized MAPbI(3) coverage.
机译:杂化有机-无机卤化物钙钛矿已经出现在可溶液处理的光伏设备的最前沿。由于钙钛矿前体混合物是物种的复杂平衡,因此很难预测/控制它们与不同底物的相互作用,因此很难预测最终的薄膜性能和器件性能。在这里,CH3NH3PbI3(MAPbI(3))在聚(3,4-乙撑二氧噻吩):聚(苯乙烯磺酸盐)(PEDOT:PSS)空穴传输层上的润湿性通过利用氧化石墨烯(GO)和葡萄糖的协同作用而得到改善。另外,葡萄糖触发了GO的减少,从而增强了PEDOT:PSS + GO +葡萄糖基纳米复合材料的电导率。通过与制造在原始PEDOT:PSS上的器件相比,制造无磁滞的MAPbI(3)太阳能电池可显示出约37%的功率转换效率提高,从而证明了该方法与光伏应用的相关性。最重要的是,V-OC达到超过1.05 V的值,这是有史以来PEDOT:PSS引脚器件体系结构报告的最高值,这表明重组损失最小,空穴选择性高,PEDOT:PSS处的陷阱密度降低以及优化的MAPbI( 3)覆盖范围。

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  • 来源
    《Advanced Functional Materials 》 |2016年第38期| 6985-6994| 共10页
  • 作者单位

    Univ Salento, Dipartimento Ingn Innovaz, Via Monteroni,Km 1, I-73100 Lecce, Italy;

    Univ Salento, Dipartimento Matemat & Fis E De Giorgi, Via Arnesano SNC, I-73100 Lecce, Italy|Ist Italiano Tecnol, Ctr Biomol Nanotechnol CBN Fdn, Via Barsanti 14, I-73010 Lecce, Italy|CNR Nanotec, Ist Nanotecnol, Polo Nanotecnol, Campus Ecotekne,Via Monteroni, I-73100 Lecce, Italy;

    Univ Salento, Dipartimento Matemat & Fis E De Giorgi, Via Arnesano SNC, I-73100 Lecce, Italy|CNR Nanotec, Ist Nanotecnol, Polo Nanotecnol, Campus Ecotekne,Via Monteroni, I-73100 Lecce, Italy;

    CNR ISOF, Ist Sintesi & Fotoreattivita, Via Gobetti 101, I-40129 Bologna, Italy;

    CNR ISOF, Ist Sintesi & Fotoreattivita, Via Gobetti 101, I-40129 Bologna, Italy;

    CNR ISOF, Ist Sintesi & Fotoreattivita, Via Gobetti 101, I-40129 Bologna, Italy;

    CNR ISOF, Ist Sintesi & Fotoreattivita, Via Gobetti 101, I-40129 Bologna, Italy;

    Univ Salento, Dipartimento Ingn Innovaz, Via Monteroni,Km 1, I-73100 Lecce, Italy;

    CNR Nanotec, Ist Nanotecnol, Polo Nanotecnol, Campus Ecotekne,Via Monteroni, I-73100 Lecce, Italy;

    Univ Salento, Dipartimento Matemat & Fis E De Giorgi, Via Arnesano SNC, I-73100 Lecce, Italy|CNR Nanotec, Ist Nanotecnol, Polo Nanotecnol, Campus Ecotekne,Via Monteroni, I-73100 Lecce, Italy;

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