Back to Search Start Over

Magnetic behaviour of bimetallic layered phases M′0.2Mn0.8PS3·0.25 H2O (M′ = ZnII, CuII, NiII, CoII).

Authors :
Fuentealba, P.
Cortes, C.
Spodine, E.
Paredes-García, V.
Venegas-Yazigi, D.
Manzur, J.
Silva, I. D. A.
Magon, C. J.
de Santana, R. C.
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry; 11/7/2017, Vol. 46 Issue 41, p14373-14381, 9p
Publication Year :
2017

Abstract

In this work the magnetic properties of bimetallic phases M′<subscript>0.2</subscript>Mn<subscript>0.8</subscript>PS<subscript>3</subscript>·0.25H<subscript>2</subscript>O (M′ = Co<superscript>II</superscript>, Ni<superscript>II</superscript>, Cu<superscript>II</superscript> or Zn<superscript>II</superscript>) have been explored and compared with those of the pristine phase MnPS<subscript>3</subscript>. Magnetic susceptibility, high field magnetization and electron paramagnetic resonance (EPR) studies reveal that the transition temperature between the antiferromagnetic and paramagnetic order for the pristine phase is shifted to lower values in the bimetallic phases. From magnetization measurements the critical field of the spin-flop transition is found to be dependent on the nature of the added secondary transition metal ion. EPR spectra of all compounds in the temperature range of 8–300 K present a single resonance line shape. Temperature dependence of the EPR parameters, like line width, g values and double integrated area (I<subscript>DIN</subscript>), are obtained from the spectra and present a scenario compatible with the magnetization results. The temperature dependence of the first derivative of the product (I<subscript>DIN</subscript>T) shows two maxima for all samples, with exception of the Co<superscript>II</superscript> phase, indicating two critical temperatures, while these critical temperatures could not be clearly determined by dc susceptibility. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
46
Issue :
41
Database :
Complementary Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
125881961
Full Text :
https://doi.org/10.1039/c7dt03249h