Department of Theoretical Chemistry, Vrije Universiteit , 1081 HV Amsterdam Netherlands.
ARC Centre of Excellence in Exciton Science, and Department of Materials Science and Engineering, Monash University , Clayton, Victoria 3800, Australia.
J Am Chem Soc. 2017 Mar 8;139(9):3456-3464. doi: 10.1021/jacs.6b11328. Epub 2017 Feb 24.
In this work, we present a combined experimental and theoretical analysis of two-component ligand shells passivating CdSe quantum dots. Using nuclear magnetic resonance spectroscopy, we first show that exposing oleate-capped quantum dots to primary carboxylic acids results in a one-for-one exchange that preserves the overall ligand surface concentration. Exposure to straight-chain acids leads to a binary ligand shell that behaves as an ideal mixture and that has a composition matching the overall acid composition of the dispersion. In the case of branched-chain acids, the exchange is restricted to about 25% of the original ligands. Based on molecular dynamics simulations, we argue that this behavior reflects the more favorable packing of oleates compared to branched carboxylates on the (100) facets of CdSe quantum dots.
在这项工作中,我们对两种组分的配体壳层对 CdSe 量子点进行了实验和理论分析。我们首先使用核磁共振波谱法表明,将油酸包覆的量子点暴露于一元羧酸中会发生一比一的交换,从而保持整体配体表面浓度不变。暴露于直链酸中会形成二元配体壳层,其表现为理想混合物,且组成与分散体中的总酸组成相匹配。对于支链酸,交换受到限制,约为原始配体的 25%。基于分子动力学模拟,我们认为这种行为反映了与 CdSe 量子点(100)面的支链羧酸相比,油酸具有更有利的堆积。