Reversible Magnetic Agglomeration: A Mechanism for Thermodynamic Control over Nanoparticle Size |
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Authors: | Dr. Grant C. Bleier Dr. John Watt Prof. Dr. Chester K. Simocko Dr. Judith M. Lavin Dr. Dale L. Huber |
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Affiliation: | 1. Sandia National Laboratories, Albuquerque, NM, USA;2. Department of Chemistry, San Jose State University, San Jose, CA, USA |
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Abstract: | We present a method for the synthesis and precise size control of magnetic nanoparticles in a reversible magnetic agglomeration mechanism. In this approach, nanoparticles nucleate and grow until a critical susceptibility is reached, in which magnetic attraction overcomes dispersive forces, leading to agglomeration and precipitation. This phase change in the system arrests nanoparticle growth and gives true thermodynamic control over the size of nanoparticles. We then show that increasing the alkyl chain length of the surfactant, and hence increasing steric stabilization, allows nanoparticles to grow to larger sizes before agglomeration occurs. Therefore, simply by choosing the correct surfactant, the size and magnetic properties of iron nanoparticles can be tailored for a particular application. With the continuous addition of the precursor solution, we can repeat the steps of nucleation, growth, and magnetic agglomeration indefinitely, making the approach suitable for large scale syntheses. |
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Keywords: | magnetic agglomeration nanoparticles synthesis thermodynamics zero-valent iron |
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