Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 121, Issue 1, Pages 801-810Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b09409
Keywords
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Funding
- U.S. National Science Foundation [CBET1511113]
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [1511113] Funding Source: National Science Foundation
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The behavior of spherical single-domain magnetic nanoparticles in strong inhomogeneous magnetic fields is investigated through Brownian dynamics simulations, taking into account magnetic dipole-dipole interactions, repulsive a, hard-core Yukawa potential, hydrodynamic particle-wall interactions, and the mechanism of magnetic dipole rotation in the presence of a magnetic field. The magnetic capture process of nanoparticles in prototypical magnetic field:gradients generated by a sudden reversal in perpendicular magnetization of a flat substrate (defining a capture line) is studied as a function of strength of the magnetic field and volume fraction of the magnetic nanoparticles. Capture curves show a regime where capture follows a power law model and suggest that particles with the Brownian relaxation mechanism are captured at a slightly faster rate than particles with the Neel relaxation mechanism under similar conditions of the field gradient. Additionally, evaluation of the shape of the aggregates of captured particles-suggests that greater dipole-dipole interactions, result in aggregate structures that are flatter/wider than in the case of negligible dipole-dipole interactions. These results can help guide the-design of systems for magnetically directed assembly of nanoparticles into complex shapes at a substrate.
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