Scaling Laws for Polymer Chains Grafted onto Nanoparticles

被引:17
|
作者
Yang, Guang [1 ,2 ]
Kim, Kyoungmin [1 ,2 ]
Wang, Wentao [3 ]
Chen, Banghao [3 ]
Mattoussi, Hedi [3 ]
Hallinan, Daniel T., Jr. [1 ,2 ]
机构
[1] Florida State Univ, Aeroprop Mechatron & Energy Ctr, 2003 Levy Ave, Tallahassee, FL 32310 USA
[2] FAMU FSU Coll Engn, Chem & Biomed Engn Dept, 2525 Pottsdamer St, Tallahassee, FL 32310 USA
[3] Florida State Univ, Dept Chem & Biochem, 95 Chieftan Way, Tallahassee, FL 32306 USA
基金
美国国家科学基金会;
关键词
gold nanoparticles; ligands; monolayers; polymer scaling law; solvent quality; GOLD NANOPARTICLES; LITHIUM BATTERIES; CURVED SURFACES; BRUSHES; PARTICLES; DYNAMICS; NANOCOMPOSITES; CONFORMATION; MONOLAYERS; MODEL;
D O I
10.1002/macp.201700417
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An experimental approach is presented for identifying the scaling laws for polymer chains grafted onto gold nanoparticles. Poly(ethylene oxide) of various molecular weights are grafted onto gold nanoparticles via thiol end-functional groups. The polymer-grafted nanoparticles are self-assembled into monolayers from solvents of different quality. Over a significant range of graft densities, nanoparticle monolayers deposited from good (athermal) solvent exhibit particle spacing that scales according to theoretical predictions for chains in dilute solution. This unexpected result for ordered nanoparticle monolayers is discussed in the context of the deposition process. In monolayers deposited from theta solvent, molecular weight scaling of particle spacing breaks down, possibly due to chain length dependence of solvent quality. In poor solvent, the structure of nanoparticle assemblies is not sufficiently ordered to obtain reliable measurements, possibly due to loss of nanoparticle dispersion. This approach opens up the possibility for accurate measurement of the effect of solvent on grafted chain scaling in nanoparticle assemblies.
引用
收藏
页数:9
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