TY - JOUR
T1 - Site-specific spin crossover in F e2Ti O4 post-spinel under high pressure up to nearly a megabar
AU - Xu, W. M.
AU - Hearne, G. R.
AU - Layek, S.
AU - Levy, D.
AU - Itié, J. P.
AU - Pasternak, M. P.
AU - Rozenberg, G. Kh
AU - Greenberg, E.
N1 - Publisher Copyright:
© 2017 American Physical Society.
PY - 2017/7/10
Y1 - 2017/7/10
N2 - X-ray diffraction studies to ∼90GPa at room temperature show that Fe2TiO4 ferrous inverse spinel undergoes the following sequence of structural transitions: cubic(Fd3-m)→∼8GPatetragonal(I41/amd)→∼16GPaorthorhombic(Cmcm)→∼55GPaorthorhombic(Pmma), at the indicated onset transition pressures. Within the Cmcm phase, site-specific spin crossover is initiated and involves only highly distorted octahedral sites constituting ∼25% of all Fe locations. This is manifest as a steeper volume decrease of ΔV/V0∼3.5% beyond ∼40GPa and an emergent diamagnetic component discerned in Fe57 Mössbauer spectroscopy at variable cryogenic temperatures. A subsequent Cmcm→Pmma Fe/Ti disorder-order reconfiguration is facilitated at sixfold coordinated (octahedral) sites. The rest of the high-spin Fe in sixfold and eightfold coordinated sites (∼75% abundance) in the Pmma phase exhibit average saturation internal magnetic fields of Hhf∼42T to ∼90GPa, typical of spin-only (orbitally quenched) Fermi-contact values. By contrast, average Hhf∼20T values, signifying unquenched orbital moments, occur below the 40-45GPa spin-crossover initiation regime in the Cmcm phase. Therefore, site-specific spin crossover invokes a cooperative lattice response and polyhedral distortions at the rest of the high-spin Fe sites, translating to 3d level (sub-band) changes and consequential orbital moment quenching. Near ∼90GPa, Fe2TiO4 is a partially spin-converted chemically ordered Pmma post-spinel having a persistent charge gap of ∼100meV. Despite structural symmetry changes, partial spin crossover and lattice compressibility, resulting in a ∼33% total reduction in unit-cell volume and corresponding 3d bandwidth broadening, strong electron correlations persist at high densification.
AB - X-ray diffraction studies to ∼90GPa at room temperature show that Fe2TiO4 ferrous inverse spinel undergoes the following sequence of structural transitions: cubic(Fd3-m)→∼8GPatetragonal(I41/amd)→∼16GPaorthorhombic(Cmcm)→∼55GPaorthorhombic(Pmma), at the indicated onset transition pressures. Within the Cmcm phase, site-specific spin crossover is initiated and involves only highly distorted octahedral sites constituting ∼25% of all Fe locations. This is manifest as a steeper volume decrease of ΔV/V0∼3.5% beyond ∼40GPa and an emergent diamagnetic component discerned in Fe57 Mössbauer spectroscopy at variable cryogenic temperatures. A subsequent Cmcm→Pmma Fe/Ti disorder-order reconfiguration is facilitated at sixfold coordinated (octahedral) sites. The rest of the high-spin Fe in sixfold and eightfold coordinated sites (∼75% abundance) in the Pmma phase exhibit average saturation internal magnetic fields of Hhf∼42T to ∼90GPa, typical of spin-only (orbitally quenched) Fermi-contact values. By contrast, average Hhf∼20T values, signifying unquenched orbital moments, occur below the 40-45GPa spin-crossover initiation regime in the Cmcm phase. Therefore, site-specific spin crossover invokes a cooperative lattice response and polyhedral distortions at the rest of the high-spin Fe sites, translating to 3d level (sub-band) changes and consequential orbital moment quenching. Near ∼90GPa, Fe2TiO4 is a partially spin-converted chemically ordered Pmma post-spinel having a persistent charge gap of ∼100meV. Despite structural symmetry changes, partial spin crossover and lattice compressibility, resulting in a ∼33% total reduction in unit-cell volume and corresponding 3d bandwidth broadening, strong electron correlations persist at high densification.
UR - http://www.scopus.com/inward/record.url?scp=85026922347&partnerID=8YFLogxK
U2 - 10.1103/PhysRevB.96.045108
DO - 10.1103/PhysRevB.96.045108
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AN - SCOPUS:85026922347
SN - 2469-9950
VL - 96
JO - Physical Review B
JF - Physical Review B
IS - 4
M1 - 045108
ER -