Spinel
ferrites, especially cobalt ferrite, have the capability of preserving
sufficient magnetization (M
s) and coercive
field (H
c). However, precise nanostructuring
is needed to sustain the steady ferrimagnetic (FiM) response with
high H
c and remnant magnetization (M
r). By a two-step process involving co-precipitation
and inert calcination, CoFe2O4 nanoparticles
(NPs) with inherent lattice strain were achieved with appreciable
magnetic anisotropy. The disordered spins on the NP surface are found
to be the key for maintaining the anisotropy and squareness (M
r/M
s) of hysteresis
loops, the extent of which is a function of the processing temperature
and NP size. The freezing of surface spins results in 2.8 and 1.2
nm thick spin glass (SG) layers for the as-prepared and 350 °C-calcined
CoFe2O4 NPs, respectively, analyzed at 5 K.
The frozen surface spins pin the core FiM spins, resulting in the
exchange bias (H
eb) coupling. At room
temperature, 20 nm NPs exhibit permanent magnet-like features with
a maximum energy product, BHmax, of 2.4 MGOe, which is
quite promising considering CoFe2O4 as an environmentally
friendly alternative to the hazardous rare-earth-based permanent magnets.
Our CoF2O4 NP ensemble delivers both intriguing
low-temperature magnetic properties having academic and technological
interests and worthwhile room-temperature features that have direct
translational relevance.