Transition to Long Range Magnetic Order in the Highly Frustrated Insulating Pyrochlore Antiferromagnet Gd2Ti2O7

Abstract

Experimental evidence from measurements of the a.c. and d.c. susceptibility, and heat capacity data show that the pyrochlore structure oxide, Gd2Ti2O7, exhibits short range order that starts developing at 30K, as well as long range magnetic order at T 1K. The Curie-Weiss temperature, θCW = -9.6K, is largely due to exchange interactions. Deviations from the Curie-Weiss law occur below 10K while magnetic heat capacity contributions are found at temperatures above 20K. A sharp maximum in the heat capacity at Tc=0.97K signals a transition to a long range ordered state, with the magnetic specific accounting for only 50% of the magnetic entropy. The heat capacity above the phase transition can be modeled by assuming that a distribution of random fields acts on the 8S7/2 ground state for Gd3+. There is no frequency dependence to the a.c. susceptibility in either the short range or long range ordered regimes, hence suggesting the absence of any spin-glassy behavior. Mean field theoretical calculations show that no long range ordered ground state exists for the conditions of nearest-neighbor antiferromagnetic exchange and long range dipolar couplings. At the mean-field level, long range order at various commensurate or incommensurate wave vectors is found only upon inclusion of exchange interactions beyond nearest-neighbor exchange and dipolar coupling. The properties of Gd$2Ti2O7 are compared with other geometrically frustrated antiferromagnets such as the Gd3Ga5O12 gadolinium gallium garnet, RE2Ti2O7 pyrochlores where RE = Tb, Ho and Tm, and Heisenberg-type pyrochlore such as Y2Mo2O7, Tb2Mo2O7, and spinels such as ZnFe2O4

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