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Magnetochromic sensing and size-dependent collective excitations in iron oxide nanoparticles
Author(s) -
Kenneth R. O’Neal,
Jonathan M. Patete,
Peng Chen,
Ruhani Nanavati,
B. S. Holinsworth,
Jacqueline Smith,
C. Marques,
J. W. Simonson,
M. C. Aronson,
Stephen McGill,
Stanislaus S. Wong,
J. L. Musfeldt
Publication year - 2017
Publication title -
physical review. b./physical review. b
Language(s) - English
Resource type - Journals
eISSN - 2469-9969
pISSN - 2469-9950
DOI - 10.1103/physrevb.95.125416
Subject(s) - superparamagnetism , antiferromagnetism , nanoscopic scale , condensed matter physics , particle size , quasiparticle , nanoparticle , physics , spin (aerodynamics) , charge ordering , charge (physics) , coupling (piping) , materials science , nanotechnology , magnetization , chemistry , quantum mechanics , magnetic field , thermodynamics , superconductivity , metallurgy
We combine optical and magneto-optical spectroscopies with complementary vibrational and magnetic property measurements to reveal finite length scale effects in nanoscale $\ensuremath{\alpha}\ensuremath{-}{\mathrm{Fe}}_{2}{\mathrm{O}}_{3}$. Analysis of the $d$-to-$d$ on-site excitations uncovers enhanced color contrast at particle sizes below approximately 75 nm due to size-induced changes in spin-charge coupling that are suppressed again below the superparamagnetic limit. These findings provide a general strategy for amplifying magnetochromism in $\ensuremath{\alpha}\ensuremath{-}{\mathrm{Fe}}_{2}{\mathrm{O}}_{3}$ and other iron-containing nanomaterials that may be useful for advanced sensing applications. We also unravel the size dependence of collective excitations in this iconic antiferromagnet.

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