Binding and Packing in Two-Component Colloidal Quantum Dot Ligand Shells: Linear versus Branched Carboxylates

被引:61
作者
De Nolf, Kim [1 ,2 ]
Cosseddu, Salvatore M. [4 ]
Jasieniak, Jacek J. [5 ,6 ]
Drijvers, Emile [1 ,2 ]
Martins, Jose C. [3 ]
Infante, Ivan [4 ]
Hens, Zeger [1 ,2 ]
机构
[1] Univ Ghent, Phys & Chem Nanostruct, B-9000 Ghent, Belgium
[2] Univ Ghent, Ctr Nano & Biophoton, B-9000 Ghent, Belgium
[3] Univ Ghent, NMR & Struct Anal Unit, B-9000 Ghent, Belgium
[4] Vrije Univ Amsterdam, Dept Theoret Chem, NL-1081 HV Amsterdam, Netherlands
[5] Monash Univ, ARC Ctr Excellence Exciton Sci, Clayton, Vic 3800, Australia
[6] Monash Univ, Dept Mat Sci & Engn, Clayton, Vic 3800, Australia
基金
欧盟地平线“2020”; 澳大利亚研究理事会;
关键词
GOLD NANOPARTICLES; MOLECULAR-DYNAMICS; CDSE NANOCRYSTALS; HOT INJECTION; EXCHANGE; GROWTH; DISPLACEMENT; MONOLAYERS; DOMAINS; SOLUTE;
D O I
10.1021/jacs.6b11328
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 oleatecapped 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.
引用
收藏
页码:3456 / 3464
页数:9
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