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Phys. Rev. B 74, 014430 (2006) [12 pages]

Complex magnetic order in the kagomé staircase compound Co3V2O8

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Y. Chen
NIST Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA and Department of Materials Science and Engineering, University of Maryland, College Park, Maryland 20742, USA

J. W. Lynn, Q. Huang, F. M. Woodward, and T. Yildirim
NIST Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA

G. Lawes
Department of Physics and Astronomy, Wayne State University, Detroit, Michigan 48201, USA

A. P. Ramirez
Bell Labs, Lucent Technologies, 600 Mountain Avenue, Murray Hill, New Jersey 07974, USA

N. Rogado
Department of Chemistry and Princeton Materials Institute, Princeton University, Princeton, New Jersey 08544, USA and DuPont Central Research and Development, Experimental Station, Wilmington, Delaware 19880-0328, USA

R. J. Cava
Department of Chemistry and Princeton Materials Institute, Princeton University, Princeton, New Jersey 08544, USA

A. Aharony and O. Entin-Wohlman
School of Physics and Astronomy, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 69978, Israel and Department of Physics, Ben Gurion University, Beer Sheva 84105, Israel

A. B. Harris
Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA

Received 18 April 2006; revised 30 May 2006; published 25 July 2006

Co3V2O8 (CVO) has a different type of geometrically frustrated magnetic lattice, a kagomé staircase, where the full frustration of a conventional kagomé lattice is partially relieved. The crystal structure consists of two inequivalent (magnetic) Co sites, one-dimensional chains of Co(2) spine sites, linked by Co(1) cross-tie sites. Neutron powder diffraction has been used to solve the basic magnetic and crystal structures of this system, while polarized and unpolarized single crystal diffraction measurements have been used to reveal a rich variety of incommensurate phases, interspersed with lock-in transitions to commensurate phases. CVO initially orders magnetically at 11.3 K into an incommensurate, transversely polarized, spin density wave state, with wave vector k=(0,δ,0) with δ=0.55 and the spin direction along the a axis. δ is found to decrease monotonically with decreasing temperature and then locks into a commensurate antiferromagnetic structure with δ=1/2 for 6.9<T<8.6 K. In this phase, there is a ferromagnetic layer where the spine site and cross-tie sites have ordered moments of 1.39 μB and 1.17 μB, respectively, and an antiferromagnetic layer where the spine-site has an ordered moment of 2.55 μB, while the cross-tie sites are fully frustrated and have no observable ordered moment. Below 6.9 K, the magnetic structure becomes incommensurate again, and the presence of higher-order satellite peaks indicates that the magnetic structure deviates from a simple sinusoid. δ continues to decrease with decreasing temperature and locks in again at δ=1/3 over a narrow temperature range (6.2<T<6.5 K). The system then undergoes a strongly first-order transition to the ferromagnetic ground state (δ=0) at Tc=6.2 K. The ferromagnetism partially relieves the cross-tie site frustration, with ordered moments on the spine-site and cross-tie sites of 2.73 μB and 1.54 μB, respectively. The spin direction for all spins is along the a axis (Ising-like behavior). A dielectric anomaly is observed around the ferromagnetic transition temperature of 6.2 K, demonstrating that there is significant spin-charge coupling present in CVO. A theory based on group theory analysis and a minimal Ising model with competing exchange interactions can explain the basic features of the magnetic ordering.

© 2006 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.74.014430
DOI:
10.1103/PhysRevB.74.014430
PACS:
75.25.+z, 75.30.Kz, 77.84.−s, 75.10.−b