A theoretical study of dispersion-to-aggregation of nanoparticles in adsorbing polymers using molecular dynamics simulations
Source abstract
Abstract
The properties of polymer-nanoparticle (NP) mixtures significantly depend on the dispersion of the NPs. Using molecular dynamics simulations, we demonstrate that, in the presence of polymer-NP attraction, the dispersion of NPs in semidilute and concentrated polymers can be stabilized by increasing the polymer concentration. A lower polymer concentration facilitates the aggregation of NPs bridged by polymer chains, as well as a further increase of the polymer-NP attraction. Evaluating the binding of NPs through shared polymer segments in an adsorption blob, we derive a linear relationship between the polymer concentration and the polymer-NP attraction at the phase boundary between dispersed and aggregated NPs. Our theoretical findings are directly relevant for understanding and controlling many self-assembly processes that use either dispersion or aggregation of NPs to yield the desired materials.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Electrostatics and Colloid Interactions · Surfactants and Colloidal Systems · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics
Zhejiang Sci-Tech University
Hangzhou 310018, P.R. China
Department of Physics and ITPA
Xiamen University
Xiamen 361005, P.R. China
Leibniz-Institut für Polymerforschung Dresden
01069 Dresden, Germany
Department of Engineering Materials University of Sheffield Mappin Street
Sheffield S1 3JD, UK
Technische Universität Dresden
Institute of Theoretical Physics
D-01069 Dresden, Germany
References (23)
Show source-provided references
1. Yan · Prog. Polym. Sci. · 2013 · 38 · 36910.1016/j.progpolymsci.2012.05.001 ↗
2. Sun · J. Am. Chem. Soc. · 2002 · 124 · 288410.1021/ja0176503 ↗
3. Stuart · Nat. Mater. · 2010 · 9 · 10110.1038/nmat2614 ↗
4. Kim · Nat. Commun. · 2012 · 3 · 121610.1038/ncomms2218 ↗
5. Srivastava · Adv. Mater. · 2014 · 26 · 20110.1002/adma.201303070 ↗
6. Stamm · Nat. Mater. · 2007 · 6 · 26010.1038/nmat1880 ↗
7. Cao · ACS Nano · 2013 · 7 · 992010.1021/nn4037738 ↗
8. Feng · Nat. Mater. · 2015 · 14 · 6110.1038/nmat4109 ↗
9. Kremer · J. Chem. Phys. · 1990 · 92 · 505710.1063/1.458541 ↗
10. Cao · Soft Matter · 2013 · 9 · 591610.1039/c3sm50495f ↗
11. Omari · J. Phys. Chem. B · 2009 · 113 · 844910.1021/jp9035088 ↗
12. Plimpton · J. Comput. Phys. · 1995 · 117 · 110.1006/jcph.1995.1039 ↗
13. Dünweg · Int. J. Mod. Phys. C · 1991 · 02 · 81710.1142/S0129183191001037 ↗
14. Cao · Phys. Rev. E: Stat. Phys., Plasmas, Fluids, Relat. Interdiscip. Top. · 2011 · 84 · 04180210.1103/PhysRevE.84.041802 ↗
15. H. N. W. Lekkerkerker and R.Tuinier , Colloids and the Depletion Interaction , Springer , Dordrecht, Heidelberg, London, New York , 201110.1007/978-94-007-1223-2 ↗
16. De Gennes · J. Phys. · 1976 · 37 · 144510.1051/jphys:0197600370120144500 ↗
17. Eisenriegler · J. Chem. Phys. · 1982 · 77 · 629610.1063/1.443835 ↗
18. De Gennes · J. Phys., Lett. · 1983 · 44 · 24110.1051/jphyslet:01983004407024100 ↗
19. Bouchaud · J. Phys. · 1987 · 48 · 199110.1051/jphys:0198700480110199100 ↗
20. Jun · Phys. Rev. Lett. · 2007 · 98 · 12830310.1103/PhysRevLett.98.128303 ↗
21. McFarlane · Langmuir · 2010 · 26 · 1382310.1021/la101907s ↗
22. Shimanovich · ACS Nano · 2015 · 9 · 4310.1021/nn504869d ↗
23. Mun · Langmuir · 2014 · 30 · 30810.1021/la4029035 ↗