Solitary excitations and domain-wall movement in the two-dimensional canted antiferromagnet (C2N2H10)12FePO4(OH)

Natasha A. Chernova, Yanning Song, Peter Y. Zavalij, and M. Stanley Whittingham
Phys. Rev. B 70, 144405 – Published 13 October 2004

Abstract

The magnetic properties of the layered compound (C2N2H10)12FePO4(OH) have been studied using dc magnetization and ac susceptibility measurements. The compound orders as a canted antiferromagnet at Tc=29.6K. The crossover in critical exponent of magnetization from β1=0.19 to β2=0.30 is observed and attributed to the change of magnetic lattice dimensionality from 2 at low temperature to 3 just below Tc. The formation of net magnetic moment and magnetic domains below Tc is evidenced by an irreversible behavior of the dc magnetization, the presence of absorption component in the ac susceptibility, and complicated relaxation phenomena observed down to 15K. Applying Cole-Cole analysis to the frequency dependences of dispersion χ and absorption χ, two relaxation processes were distinguished in the paramagnetic and ordered phases; the temperature dependences of their relaxation times were analyzed. The faster relaxation process is described by a scaling law above Tc, and by a steady decrease of the relaxation time in the ordered phase. This process is related to the existence of solitons in the magnetic chains forming the two-dimensional layers. The slower process follows the Vogel-Fulcher law in the paramagnetic phase and the Arrhenius law with the activation energy Ea83K in the ordered phase. This process is attributed to the formation of magnetic domains and domain-wall movement. The mechanism of these processes is proposed and related to the crystal structure of the material.

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  • Received 31 March 2004

DOI:https://doi.org/10.1103/PhysRevB.70.144405

©2004 American Physical Society

Authors & Affiliations

Natasha A. Chernova*, Yanning Song, Peter Y. Zavalij, and M. Stanley Whittingham

  • Institute for Materials Research, State University of New York at Binghamton, Binghamton, New York 13902-6000, USA

  • *Electronic address: chernova@binghamton.edu

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Vol. 70, Iss. 14 — 1 October 2004

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