Effect of Polymer Chain Length on the Superlattice Assembly of Functionalized Gold Nanoparticles

被引:11
|
作者
Kim, Hyeong Jin [1 ,2 ]
Wang, Wenjie [3 ]
Zhang, Honghu [4 ]
Freychet, Guillaume [5 ]
Ocko, Benjamin M. [5 ]
Travesset, Alex [1 ,2 ]
Mallapragada, Surya K. [1 ,2 ]
Vaknin, David [1 ,2 ]
机构
[1] Iowa State Univ, Ames Lab, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Chem & Biol Engn, Ames, IA 50011 USA
[3] US DOE, Ames Lab, Div Mat Sci & Engn, Ames, IA 50011 USA
[4] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[5] Brookhaven Natl Lab, NSLS 2, Upton, NY 11973 USA
关键词
CRYSTALLIZATION; RULES; FORM;
D O I
10.1021/acs.langmuir.1c01547
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report on the assembly of gold nanoparticle (AuNPs) superlattices at the liquid/vapor interface and in the bulk of their suspensions. Interparticle distances in the assemblies are achieved on multiple length scales by varying chain lengths of surface grafted AuNPs by polyethylene glycol (PEG) with molecular weights in the range 2000-40,000 Da. Crystal structures and lattice constants in both 2D and 3D assemblies are determined by synchrotron-based surface-sensitive and small-angle X-ray scattering. Assuming knowledge of grafting density, we show that experimentally determined interparticle distances are adequately modeled by spherical brushes close to the theta point (Flory-Huggins parameter, chi approximate to 1/2) for 2D superlattices at a liquid interface and a nonsolvent (chi = infinity) for the 3D dry superlattices.
引用
收藏
页码:10143 / 10149
页数:7
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