DNA-Directed Non-Langmuir Deposition of Programmable Atom Equivalents

Particle assembly at interfaces via programmed DNA interactions allows for independent modification of both nanoparticle-surface interaction strength and the magnitude of interparticle repulsion. Together, these factors allow for modification of the deposited thin film morphology via alterations in...

Full description

Bibliographic Details
Main Authors: Lewis, Diana Jean (Author), Gabrys, Paul Anthony (Author), Macfarlane, Robert J (Author)
Other Authors: Massachusetts Institute of Technology. Department of Aeronautics and Astronautics (Contributor), Massachusetts Institute of Technology. Department of Materials Science and Engineering (Contributor)
Format: Article
Language:English
Published: American Chemical Society (ACS), 2020-10-01T13:56:18Z.
Subjects:
Online Access:Get fulltext
LEADER 02553 am a22002293u 4500
001 127781
042 |a dc 
100 1 0 |a Lewis, Diana Jean  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Aeronautics and Astronautics  |e contributor 
100 1 0 |a Massachusetts Institute of Technology. Department of Materials Science and Engineering  |e contributor 
700 1 0 |a Gabrys, Paul Anthony  |e author 
700 1 0 |a Macfarlane, Robert J  |e author 
245 0 0 |a DNA-Directed Non-Langmuir Deposition of Programmable Atom Equivalents 
260 |b American Chemical Society (ACS),   |c 2020-10-01T13:56:18Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/127781 
520 |a Particle assembly at interfaces via programmed DNA interactions allows for independent modification of both nanoparticle-surface interaction strength and the magnitude of interparticle repulsion. Together, these factors allow for modification of the deposited thin film morphology via alterations in DNA binding sequence. Importantly, both Langmuir and random sequential adsorption models yield insights into the thermodynamics of deposition but cannot fully explain particle coverage as a function of all relevant variables, indicating that the particle deposition mechanism for DNA-grafted colloids is more complex than prior adsorption phenomena. Here, it is shown that these deviations from standard behavior arise from the fact that each nanoparticle is attached to the surface via multiple weak DNA duplex interactions, enabling diffusion of adsorbed colloids across the substrate. Thus, surface migration of individual particles causes reorganization of the deposited monolayer, leading to the unusual behavior of coverage increasing at elevated temperatures that are just below the particle desorption temperature. The programmability of DNA-directed particle deposition therefore allows for precise control over the morphology of monolayer films, as well as the ability to generate crystalline materials with controllable surface roughness and grain size through layer-by-layer growth. The increased control over thin film morphology potentially enables tailoring of mechanical and optical properties and holds promise for use in a variety of applications. 
520 |a United States. Department of Energy. Office of Science (Contract DE-AC02-06CH11357) 
520 |a National Science Foundation (U.S.). Graduate Research Fellowship Program (Grant NSF 1122374) 
546 |a en 
655 7 |a Article 
773 |t 10.1021/ACS.LANGMUIR.8B01541 
773 |t Langmuir