72 research outputs found
Scaling of transverse nuclear magnetic relaxation due to magnetic nanoparticle aggregation
The aggregation of superparamagnetic iron oxide (SPIO) nanoparticles
decreases the transverse nuclear magnetic resonance (NMR) relaxation time T2 of
adjacent water molecules measured by a Carr-Purcell-Meiboom-Gill (CPMG)
pulse-echo sequence. This effect is commonly used to measure the concentrations
of a variety of small molecules. We perform extensive Monte Carlo simulations
of water diffusing around SPIO nanoparticle aggregates to determine the
relationship between T2 and details of the aggregate. We find that in the
motional averaging regime T2 scales as a power law with the number N of
nanoparticles in an aggregate. The specific scaling is dependent on the fractal
dimension d of the aggregates. We find T2 N^{-0.44} for aggregates with d=2.2,
a value typical of diffusion limited aggregation. We also find that in
two-nanoparticle systems, T2 is strongly dependent on the orientation of the
two nanoparticles relative to the external magnetic field, which implies that
it may be possible to sense the orientation of a two-nanoparticle aggregate. To
optimize the sensitivity of SPIO nanoparticle sensors, we propose that it is
best to have aggregates with few nanoparticles, close together, measured with
long pulse-echo times.Comment: 20 pages, 3 figures, submitted to Journal of Magnetism and Magnetic
Material
Fabrication and Characterization of Modulation-Doped ZnSe/(Zn,Cd)Se (110) Quantum Wells: A New System for Spin Coherence Studies
We describe the growth of modulation-doped ZnSe/(Zn,Cd)Se quantum wells on
(110) GaAs substrates. Unlike the well-known protocol for the epitaxy of
ZnSe-based quantum structures on (001) GaAs, we find that the fabrication of
quantum well structures on (110) GaAs requires significantly different growth
conditions and sample architecture. We use magnetotransport measurements to
confirm the formation of a two-dimensional electron gas in these samples, and
then measure transverse electron spin relaxation times using time-resolved
Faraday rotation. In contrast to expectations based upon known spin relaxation
mechanisms, we find surprisingly little difference between the spin lifetimes
in these (110)-oriented samples in comparison with (100)-oriented control
samples.Comment: To appear in Journal of Superconductivity (Proceedings of 3rd
Conference on Physics and Applications of Spin-dependent Phenomena in
Semiconductors
Integrated diagnostics: proceedings from the 9th biennial symposium of the International Society for Strategic Studies in Radiology
published_or_final_versio
Scalable Synthesis of Janus Particles with High Naturality
Because of the increasing concerns about the ecological damage and negative health effects that may be caused by petrochemical-based microbeads, many countries are banning their use in a wide range of consumer products. One particular class of particles that may never reach their full potential because of such a ban is Janus particles, which are particles with two opposite properties. Despite significant progress in the scalable synthesis of Janus particles, most studies rely on petrochemical-based materials and solvents to enable their synthesis. In this report, we present a single-emulsion polymerization method for scalable synthesis of amphiphilic Janus particles with materials derived from plants. Soybean oil-epoxidized acrylate (SBOEA) monomers are polymerized in single-emulsion droplets of SBOEA, ethyl cellulose (EC), butyl acetate, and initiators that can be generated by either bulk or microfluidic emulsification, leading to the formation of amphiphilic soybean oil polymer/EC (SBOP/EC) Janus particles. Interfacial anchoring of the in situ-formed SBOP particles at the interface of the emulsion droplet plays a key role in the formation of the SBOP/EC Janus particles. Large-scale preparation of uniform SBOP/EC Janus particles is also demonstrated using a glass-silicon microfluidic device. Finally, the SBOP/EC Janus particles show potential to stabilize oil-in-water emulsions that can stay stable under flowing conditions
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