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Influence of metallic and dielectric nanowire arrays on the photoluminescence properties of P3HT thin films

机译:金属和介电纳米线阵列对P3HT薄膜光致发光性能的影响

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摘要

The optical properties of organic semiconductor thin films deposited on nanostructured surfaces are investigated using time-resolved two-photon photoluminescence (PL) microscopy. The surfaces consist of parallel aligned metallic or dielectric nanowires forming well-defined arrays on glass substrates. Keeping the nanowire dimensions constant and varying only their spacing from 40 to 400nm, we study the range of different types of nanowire-semiconductor interactions. For silver nanowires and spacings below 100nm, the PL intensity and lifetime of P3HT and MDMO-PPV decrease rapidly due to the short-ranged metal-induced quenching that dominates the PL response with respect to a possible plasmonic enhancement of optical transition rates. In the case of P3HT however, we observe an additional longer-ranged reduction of non-radiative losses for both metallic and dielectric nanowires that is not observed for MDMO-PPV. Excitation polarization dependent measurements indicate that this reduction is due to self-assembly of the P3HT polymer chains along the nanowires. In conclusion, nanostructured surfaces, when fabricated across large areas, could be used to control film morphologies and to improve energy transport and collection efficiencies in P3HT-based solar cells.
机译:使用时间分辨双光子光致发光(PL)显微镜研究了沉积在纳米结构表面上的有机半导体薄膜的光学特性。这些表面由平行排列的金属或电介质纳米线组成,在玻璃基板上形成清晰的阵列。保持纳米线尺寸恒定并且仅在40至400nm之间改变其间距,我们研究了不同类型的纳米线-半导体相互作用的范围。对于间距小于100nm的银纳米线,P3HT和MDMO-PPV的PL强度和寿命迅速降低,这是由于短程金属诱导的猝灭作用主导着PL响应,而光子跃迁可能是等离激元的增强。但是,在P3HT的情况下,我们观察到金属和电介质纳米线的非辐射损耗有更长距离的减少,而MDMO-PPV则没有。激发极化相关的测量结果表明,这种减少是由于P3HT聚合物链沿纳米线的自组装所致。总之,当在大面积上制造纳米结构表面时,可用于控制膜的形态并提高基于P3HT的太阳能电池的能量传输和收集效率。

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