Thermodynamics of Composition Dependent Ligand Exchange on the Surfaces of Colloidal Indium Phosphide Quantum Dots

被引:38
|
作者
Calvin, Jason J. [1 ,2 ]
O'Brien, Erin A. [1 ,2 ]
Sedlak, Adam B. [1 ]
Balan, Arunima D. [1 ,2 ]
Alivisatos, A. Paul [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
[3] Kavli Energy NanoScieoce Inst, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
indium phosphide; isothermal titration calorimetry; H-1 NMR titrations; Ising model; interligand interactions; colupowion dependent binding; NANOCRYSTALS; INP; BINDING; NMR; DISPLACEMENT; GROWTH; GOLD; PHOTOLUMINESCENCE; HETEROGENEITY; LUMINESCENCE;
D O I
10.1021/acsnano.0c08683
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quantum dot surfaces can have a substantial effect on their physical, chemical, and optoelectronic properties. When the chemistry that occurs at the surface of nanocrystals is studied, critical insights can be gained into the fundamental structural, thermodynamic, and optical properties of quantum dot materials providing a valuable guide for how to best adapt them for desired applications. Colloidal quantum dots are often terminated with organic ligands that consist of a long aliphatic chain and a head group that binds tightly to the nanocrystal surface. While extensive work has been done to understand how ligand head groups influence quantum dot properties, studies to unravel the influence of the organic ligand tail on ligands and surface reaction equilibria are incomplete. To further investigate the driving forces of quantum dot surface modification, a series of ligand exchange reactions with oleic acid were performed on indium phosphide quantum dots, initially terminated with straight-chain carboxylates of variable lengths. The reaction was monitored using isothermal titration calorimetry and H-1 NMR to determine the extent of each reaction and its associated thermodynamics. From these measurements, interligand interactions were observed to be dependent on the length of the straight-chain ligand. A modified Ising model was used to investigate the enthalpic and entropic effects contributing to these ligand exchanges and reveal that interligand interactions play a much larger role than previously thought. Additional experimentation with phosphonic acid ligand exchange reveals complexity in the reaction mechanism but further illustrates the significant impact of ligand tail group length on thermodynamics, even in cases where there is a large difference in head group binding energy.
引用
收藏
页码:1407 / 1420
页数:14
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