Self-limiting gold nanoparticle surface assemblies through modulation of pH and ionic strength
Autor: | Richard A. Vaia, Michael L. Jespersen, John J. Kelley |
---|---|
Rok vydání: | 2018 |
Předmět: |
Materials science
Nanoparticle Bioengineering Self-assembled monolayer 02 engineering and technology General Chemistry 010402 general chemistry 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences Atomic and Molecular Physics and Optics 0104 chemical sciences Adsorption Chemical engineering Ionic strength Colloidal gold Modeling and Simulation Monolayer Surface modification Particle General Materials Science 0210 nano-technology |
Zdroj: | Journal of Nanoparticle Research. 20 |
ISSN: | 1572-896X 1388-0764 |
DOI: | 10.1007/s11051-018-4388-y |
Popis: | Techniques to assemble monolayers of nanoparticles on surfaces are crucial for manufacturing devices for applications ranging from bio-sensing to tribology. Electrostatic-mediated assembly has numerous potential attributes, including self-limiting deposition and the ability to tune nanoparticle density and order through solution conditions. Herein, we establish the synergistic role of pH, ionic strength (I), and particle functionalization to identify the conditions for electrostatic assembly that yield maximum process stability and particle coverage. When the particle and surface are oppositely charged, the density of adsorbed 11.4-nm gold nanoparticles (AuNPs) could be tuned with both pH and ionic strength. The resulting monolayer arrays were disordered, in agreement with random sequential adsorption (RSA) theory. Finally, AuNPs stabilized by associated citrate molecules provided a larger processing window (pH 3–9, I = 1–10 mM) than AuNPs capped with a covalently bound mercaptopropanesulfonate (MPS) ligand shell (pH 3–9, I = 0.1–5 mM). These processing regimes provide a standard for predicting structural formations at reduced particle-surface interactions. |
Databáze: | OpenAIRE |
Externí odkaz: |