Published February 2013 | Version v1
Journal article

Hydrothermal syntheses and low temperature magnetic behaviors of ACo3(P2O7)2 (A=Ca, Sr, Ba, Pb)

  • 1. Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)
  • 2. College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China)

Description

ACo3(P2O7)2 (A=Ca, Sr, Ba, Pb) has been synthesized hydrothermally. Dc and ac magnetic susceptibilities are measured at various conditions. The magnetic interactions in all four compounds are dominantly ferromagnetic. All four compounds has a ferromagnetic-like long-range ordering at 8.0 K for CaCo, 6.4 K for SrCo, 7.6 K for PbCo, 8.0 K for BaCo. The ordering of PbCo at 7.6 K may contain a glassy component. Moreover, there is an additional phase transition for PbCo at 3.6 K. Once enhancing the external field to 3 kOe, the second phase transition is suppressed. Isothermal magnetizations of SrCo, PbCo and BaCo are quite similar, showing a field-induced metamagnetic transition at 2 K. For PbCo, the low-field ground state is weak ferromagnetic, and the critical filed is 10 kOe. Differently, CaCo is a typical soft weak ferromagnet. - Graphical abstract: Dc and ac magnetic susceptibilities were measured on ACo3P4O14 (A=Ca, Sr, Ba, Pb). At 2 K, PbCo3P4O14 is a field-induced metamagnet, while CaCo3P4O14 is a soft ferromagnet. Highlights: ► Pure ACo3(P2O7)2 (A=Ca, Sr, Ba, Pb) samples are hydrothermally prepared. ► Dc and ac magnetic data shows they all have a FM-like ordering at 6–8 K. ► CaCo3(P2O7)2 is a typical soft ferromagnet. ► PbCo3(P2O7)2 has a metamagnetic transition at 2 K with a critical field of 10 kOe.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2012.09.035

Additional details

Identifiers

DOI
10.1016/j.jssc.2012.09.035;
PII
S0022-4596(12)00632-9;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
198
Journal Page Range
p. 1-5
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.