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Charge dynamics in alkanedithiols-additives in P3HT:PCBM bulk heterojunction solar cells

机译:P3HT:PCBM本体异质结太阳能电池中链烷二硫醇添加剂的电荷动力学

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Addition of a small fraction of high boiling point solvent into the host of donor/acceptor blend is one the best approach to control the morphology in order to enhance the power conversion efficiency of organic bulk heterojunction (BHJ) solar cell devices. Herein, we focus on the effect of two thiol-based additives (1,6-hexanedithiol (HDT) and 1,5-pentanedithiol (PDT)) on the charge dynamics of P3HT:PCBM blend system, studied by transient absorption spectroscopy (TAS) and correlated with the solar cell device performance. TAS reveals a more efficient charge generation and polaron formation in the systems with additives as compared to those without (NA systems), at the onset which persists up to few microseconds. The recombination dynamics also exhibits the reduced recombination losses on adding these additives in this system; however, there is marginal change of recombination dynamics in PDT added system with the control. These charge dynamics were validated using the analytical model proposed in our previous work and also correlated with improved device performance (η_(NA) = 0.9%, η_(HDT)=237%, η_(PDT)= 1.6%).
机译:为了提高有机本体异质结(BHJ)太阳能电池器件的功率转换效率,将少量高沸点溶剂添加到施主/受主混合物中是控制形态的最佳方法之一。本文中,我们通过瞬态吸收光谱法(TAS)研究了两种基于硫醇的添加剂(1,6-己二硫醇(HDT)和1,5-戊二硫醇(PDT))对P3HT:PCBM共混体系电荷动力学的影响。 ),并与太阳能电池设备的性能相关。 TAS揭示了在没有添加剂的系统中,与没有添加剂的系统(NA系统)相比,其电荷产生和极化子形成更为有效,这种现象持续时间可长达数微秒。在该系统中添加这些添加剂后,重组动力学还表现出降低的重组损失。但是,在添加了PDT的系统和控制系统中,重组动力学的变化很小。这些电荷动力学使用我们先前工作中提出的分析模型进行了验证,并且还与器件性能的改善相关(η_(NA)= 0.9%,η_(HDT)= 237%,η_(PDT)= 1.6%)。

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