TY - JOUR
T1 - Origin of the verwey transition in magnetite
AU - Rozenberg, G. Kh
AU - Paz-Pasternak, Moshe
AU - Xu, W. M.
AU - Amiel, Y.
AU - Hanfland, M.
AU - Amboage, M.
AU - Taylor, R. D.
AU - Jeanloz, R.
PY - 2006
Y1 - 2006
N2 - Comprehensive x-ray powder diffraction studies were carried out in magnetite in the 80-150 K and 0-12 GPa ranges with a membrane-driven diamond anvil cell and helium as a pressure medium. Careful data analyses have shown that a reversible, cubic to a distorted-cubic, structural transition takes place with increasing pressure, within the (P,T) regime below the Verwey temperature TV(P). The experimental documentation that TV(P)=Tdist(P) implies that the pressure-temperature-driven metal-insulator Verwey transition is caused by a gap opening in the electronic band structure due to the crystal-structural transformation to a lower-symmetry phase. The distorted-cubic insulating phase comprises a relatively small pressure-temperature range of the stability field of the cubic metallic phase that extends to 25 GPa.
AB - Comprehensive x-ray powder diffraction studies were carried out in magnetite in the 80-150 K and 0-12 GPa ranges with a membrane-driven diamond anvil cell and helium as a pressure medium. Careful data analyses have shown that a reversible, cubic to a distorted-cubic, structural transition takes place with increasing pressure, within the (P,T) regime below the Verwey temperature TV(P). The experimental documentation that TV(P)=Tdist(P) implies that the pressure-temperature-driven metal-insulator Verwey transition is caused by a gap opening in the electronic band structure due to the crystal-structural transformation to a lower-symmetry phase. The distorted-cubic insulating phase comprises a relatively small pressure-temperature range of the stability field of the cubic metallic phase that extends to 25 GPa.
UR - http://www.scopus.com/inward/record.url?scp=33144461377&partnerID=8YFLogxK
U2 - 10.1103/PhysRevLett.96.045705
DO - 10.1103/PhysRevLett.96.045705
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AN - SCOPUS:33144461377
SN - 0031-9007
VL - 96
JO - Physical Review Letters
JF - Physical Review Letters
IS - 4
M1 - 045705
ER -