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High Infrared Photoconductivity in Films of Arsenic-Sulfide-Encapsulated Lead-Sulfide Nanocrystals

机译:硫化砷包裹的硫化铅纳米晶体薄膜的高红外光电导性

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摘要

Highly photoconductive thin films of inorganic-capped PbS nanocrystal quantum dots (QDs) are reported. Stable colloidal dispersions of (NH4)3AsS3-capped PbS QDs were processed by a conventional dip-coating technique into a thin homogeneous film of electronically coupled PbS QDs. Upon drying at 130 °C, (NH4)3AsS3 capping ligands were converted into a thin layer of As2S3, acting as an infrared-transparent semiconducting glue. Photodetectors obtained by depositing such films onto glass substrates with interdigitate electrode structures feature extremely high light responsivity and detectivity with values of more than 200 A/W and 1.2 × 1013 Jones, respectively, at infrared wavelengths up to 1400 nm. Importantly, these devices were fabricated and tested under ambient atmosphere. Using a set of time-resolved optoelectronic experiments, the important role played by the carrier trap states, presumably localized on the arsenic-sulfide surface coating, has been elucidated. Foremost, these traps enable a very high photoconductive gain of at least 200. The trap state density as a function of energy has been plotted from the frequency dependence of the photoinduced absorption (PIA), whereas the distribution of lifetimes of these traps was recovered from PIA and photoconductivity (PC) phase spectra. These trap states also have an important impact on carrier dynamics, which led us to propose a kinetic model for trap state filling that consistently describes the experimental photoconductivity transients at various intensities of excitation light. This model also provides realistic values for the photoconductive gain and thus may serve as a useful tool to describe photoconductivity in nanocrystal-based solids.
机译:报道了无机封端的PbS纳米晶体量子点(QDs)的高光电导薄膜。 (NH4)3AsS3封端的PbS QD的稳定胶体分散体通过常规浸涂技术加工成电子耦合的PbS QD的均质薄膜。在130°C下干燥后,将(NH4)3AsS3封端配体转化为As2S3薄层,用作红外透明的半导体胶。通过将此类膜沉积到具有叉指电极结构的玻璃基板上而获得的光电探测器具有极高的光响应度和探测率,在高达180瓦的红外波长下其值分别超过200 A / W和1.2×10 13 Jones。 1400纳米重要的是,这些设备是在环境气氛下制造和测试的。通过一组时间分辨的光电实验,阐明了载流子陷阱态(大概位于硫化砷表面涂层上)所起的重要作用。最重要的是,这些陷阱能够实现至少200的非常高的光导增益。已经根据光致吸收(PIA)的频率依赖性绘制了陷阱态密度与能量的关系图,而这些陷阱的寿命分布从PIA和光电导(PC)相谱。这些陷阱态对载流子动力学也有重要影响,这促使我们提出了一种用于陷阱态填充的动力学模型,该模型始终描述了在各种激发光强度下的实验光电导瞬变。该模型还提供了光电导增益的实际值,因此可以用作描述纳米晶体基固体中光电导性的有用工具。

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