Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O

The work reported here is a detailed study of the proton magnetic resonance in single crystals of CoCl₂∙6H₂O. This substance is paramagnetic at high temperatures and becomes antiferromagnetic at about 2.25°K. The proton resonance frequency is a measure of the total magnetic field at the positions of...

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Main Author: Sawatzky, Erich
Language:English
Published: University of British Columbia 2011
Subjects:
Online Access:http://hdl.handle.net/2429/39158
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-391582018-01-05T17:49:33Z Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O Sawatzky, Erich Nuclear physics Dichlorohexaaquo cobalt (II) Cobaltous dichloride hexahydrate Resonance The work reported here is a detailed study of the proton magnetic resonance in single crystals of CoCl₂∙6H₂O. This substance is paramagnetic at high temperatures and becomes antiferromagnetic at about 2.25°K. The proton resonance frequency is a measure of the total magnetic field at the positions of the protons, which is the vector sum of the applied magnetic field with the internal field produced by the surrounding magnetic ions. At room temperature a single line about 6 gauss wide is observed. This line splits into a number of components at liquid helium temperatures. The position and number of lines strongly depend on temperature and on the direction of the externally applied magnetic field. The maximum overall splitting at 4.2°K is about 150 gauss in a field of 5000 gauss. At, 2.1°K the maximum splitting observed is about 2500 gauss. From the resonance lines in the paramagnetic phase it was possible to calculate the direction cosines of one proton-proton vector. The resonance spectra in both phases were found to agree well with the theory predicting the positions of the resonance lines and their dependence on crystal orientation. The transition temperature T[subscript N] was measured as a function of applied field and crystal orientation using the proton resonance lines, since they are very sensitive functions of temperature near T[subscript N]. T [subscript N] is found to be a complicated function of the applied field and crystal orientation, which cannot be described by T[subscript N](H,) = T(0) - const. H², as predicted by the Weiss Molecular field theory. The transition takes place over a temperature region of about 10[power -2] °K, and effects due to short range order are observed just above T[subscript N]. The magnetic susceptibility in zero field was measured along the preferred axis of antiferromagnetic alignment. This, together with specific heat data from published literature, was used to show a mutual consistency between thermodynamic variables and T[subscript N] obtained by NMR. The sublattice magnetization in the antiferromagnetic phase was measured as a function of temperature. It is found to depend logarithmically on T[subscript N] - T, but is independent of applied field and crystal orientation. Further experiments are suggested, which would add greatly to the understanding of the magnetic behaviour of CoCl₂∙6H₂0. Science, Faculty of Physics and Astronomy, Department of Graduate 2011-11-18T21:32:34Z 2011-11-18T21:32:34Z 1962 Text Thesis/Dissertation http://hdl.handle.net/2429/39158 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. University of British Columbia
collection NDLTD
language English
sources NDLTD
topic Nuclear physics
Dichlorohexaaquo cobalt (II)
Cobaltous dichloride hexahydrate
Resonance
spellingShingle Nuclear physics
Dichlorohexaaquo cobalt (II)
Cobaltous dichloride hexahydrate
Resonance
Sawatzky, Erich
Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O
description The work reported here is a detailed study of the proton magnetic resonance in single crystals of CoCl₂∙6H₂O. This substance is paramagnetic at high temperatures and becomes antiferromagnetic at about 2.25°K. The proton resonance frequency is a measure of the total magnetic field at the positions of the protons, which is the vector sum of the applied magnetic field with the internal field produced by the surrounding magnetic ions. At room temperature a single line about 6 gauss wide is observed. This line splits into a number of components at liquid helium temperatures. The position and number of lines strongly depend on temperature and on the direction of the externally applied magnetic field. The maximum overall splitting at 4.2°K is about 150 gauss in a field of 5000 gauss. At, 2.1°K the maximum splitting observed is about 2500 gauss. From the resonance lines in the paramagnetic phase it was possible to calculate the direction cosines of one proton-proton vector. The resonance spectra in both phases were found to agree well with the theory predicting the positions of the resonance lines and their dependence on crystal orientation. The transition temperature T[subscript N] was measured as a function of applied field and crystal orientation using the proton resonance lines, since they are very sensitive functions of temperature near T[subscript N]. T [subscript N] is found to be a complicated function of the applied field and crystal orientation, which cannot be described by T[subscript N](H,) = T(0) - const. H², as predicted by the Weiss Molecular field theory. The transition takes place over a temperature region of about 10[power -2] °K, and effects due to short range order are observed just above T[subscript N]. The magnetic susceptibility in zero field was measured along the preferred axis of antiferromagnetic alignment. This, together with specific heat data from published literature, was used to show a mutual consistency between thermodynamic variables and T[subscript N] obtained by NMR. The sublattice magnetization in the antiferromagnetic phase was measured as a function of temperature. It is found to depend logarithmically on T[subscript N] - T, but is independent of applied field and crystal orientation. Further experiments are suggested, which would add greatly to the understanding of the magnetic behaviour of CoCl₂∙6H₂0. === Science, Faculty of === Physics and Astronomy, Department of === Graduate
author Sawatzky, Erich
author_facet Sawatzky, Erich
author_sort Sawatzky, Erich
title Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O
title_short Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O
title_full Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O
title_fullStr Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O
title_full_unstemmed Proton magnetic resonance in paramagnetic and antiferromagnetic CoCl₂·6H₂O
title_sort proton magnetic resonance in paramagnetic and antiferromagnetic cocl₂·6h₂o
publisher University of British Columbia
publishDate 2011
url http://hdl.handle.net/2429/39158
work_keys_str_mv AT sawatzkyerich protonmagneticresonanceinparamagneticandantiferromagneticcocl26h2o
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