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Epitaxially Connected PbSe Quantum-Dot Films: Controlled Neck Formation and Optoelectronic Properties

机译:外延连接的PbSe量子点薄膜:受控的颈形成和光电性能

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摘要

Ligand exchange is a much-used method to increase the conductivity of colloidal quantum-dot films by replacing long insulating ligands on quantum-dot surfaces with shorter ones. Here we show that while some ligands indeed replace the original ones as expected, others may be used to controllably remove the native ligands and induce epitaxial necking of specific crystal facets. In particular, we demonstrate that amines strip lead oleate from the (100) surfaces of PbSe quantum dots. This leads to necking of QDs and results in cubic superlattices of epitaxially connected QDs. The number of amine head-groups as well as the carbon chain length of linear diamines is shown to control the extent of necking. DFT calculations show that removal of Pb(oleate)(2) from (100) surfaces is exothermic for all amines, but the driving force increases as monoamines < long diamines < short diamines < tetramines. The neck formation and cubic ordering results in a higher optical absorption cross section and higher charge carrier mobilities, thereby showing that the use of the proper multidentate amine molecules is a powerful tool to create supercrystals of epitaxially connected PbSe QDs with controlled electronic coupling.
机译:配体交换是通过用较短的配体代替量子点表面上的长绝缘配体来增加胶体量子点膜的电导率的常用方法。在这里,我们表明,尽管某些配体确实可以按预期替代原始配体,但其他配体可用于可控地去除天然配体并诱导特定晶面的外延颈缩。特别是,我们证明了胺从PbSe量子点的(100)表面剥离了油酸铅。这导致QD缩颈,并导致外延连接的QD形成立方超晶格。胺的头基数目以及线性二胺的碳链长度显示出可控制颈缩的程度。 DFT计算表明,对于所有胺,从(100)表面去除Pb(油酸酯)(2)都是放热的,但驱动力随单胺<长二胺<短二胺<四胺而增加。颈部的形成和立方有序性导致较高的光吸收截面和较高的电荷载流子迁移率,从而表明,使用适当的多齿胺分子是用受控的电子耦合产生外延连接的PbSe QD超晶的有力工具。

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