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Impact of Hole Transport Layer Surface Properties on the Morphology of a Polymer-Fullerene Bulk Heterojunction

机译:空穴传输层表面性质对聚合物-富勒烯本体异质结形态的影响

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摘要

Investigations on the impact of interfacial modification on organic optoelectronic device performance often attribute the improved device performance to the optoelectronic properties of the modifier. A critical assumption of such conclusions is that the organic active layer deposited on top of the modified surface (interface) remains unaltered. Here the validity of this assumption is investigated by examining the impact of substrate surface properties on the morphology of poly(3-hexylthiophene):1-(3-methoxycarbonyl)-propyl-1-phenyl-[6,6]C61 (P3HT:PCBM) bulk-heterojunction (BHJ). A set of four nickel oxide and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) hole transport layers (HTL) with contrasting surface properties and performance in organic photovoltaic (OPV) devices is studied. Differences in vertical composition variation and structural morphologies are observed across the samples, but only in the near-interface region of <∼20 nm. Near-interface differences in morphology are most closely correlated with surface polarity and surface roughness of the HTL. Surface polarity is more influenced by surface composition than surface roughness and crystal structure. These findings corroborate the previously mentioned conclusions that the differences in device performance observed in solar cells employing these HTLs are dominated by the electronic properties of the HTL/organic photoactive active layer interface and not by unintentional alteration in the BHJ active layer morphology.
机译:关于界面改性对有机光电器件性能的影响的研究通常将改进的器件性能归因于改性剂的光电性能。这些结论的关键假设是沉积在改性表面(界面)顶部的有机活性层保持不变。在此,通过检查基材表面性质对聚(3-己基噻吩):1-(3-甲氧基羰基)-丙基-1-苯基-[6,6] C61(P3HT: PCBM)本体异质结(BHJ)。研究了一组四个氧化镍和聚(3,4-乙撑二氧噻吩):聚(苯乙烯磺酸盐)(PEDOT:PSS)空穴传输层(HTL),它们在有机光伏(OPV)器件中具有相反的表面性质和性能。在整个样品中观察到垂直组成变化和结构形态的差异,但仅在<〜20 nm的近界面区域。形态上的近界面差异与HTL的表面极性和表面粗糙度最密切相关。与表面粗糙度和晶体结构相比,表面极性受表面成分的影响更大。这些发现证实了先前提到的结论:在采用这些HTL的太阳能电池中观察到的器件性能差异主要由HTL /有机光敏活性层界面的电子特性决定,而不是由BHJ活性层形态的无意改变所决定。

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