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Please use this identifier to cite or link to this item:
http://hdl.handle.net/1842/4920
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| Title: | Synthesis and physical properties of low dimensional quantum magnets |
| Authors: | Nilsen, Gøran Jan |
| Supervisor(s): | Rønnow, Henrik M. Harrison, Andrew Attfield, John |
| Issue Date: | 25-Nov-2010 |
| Publisher: | The University of Edinburgh |
| Abstract: | Strong electron correlation lies at the root of many quantum collective phenomena
observed in solids, including high Tc superconductivity. Theoretically, the problem of
many interacting electrons is difficult to treat, however, and a microscopic understanding
of strongly correlated systems remains one of the foremost challenges in modern
physics. A particularly clean realisation of this general problem is found in magnetic
systems, where theory and experiment are both well developed and complementary.
The role of the chemist in this endeavour is to provide model experimental systems to
both inspire new developments in theory and to confirm existing predictions. This thesis
aims to demonstrate aspects of both synthesis and physical characterisation of such
model systems, with particular emphasis on materials which exhibit unusual quantum
ground states due to a combination of reduced dimensionality, low spin, and geometric
frustration. Four materials are considered: The first among these is a new material,
KTi(SO4)2·(H2O), which was prepared using a hydrothermal route, and characterised
by magnetic susceptibility, specific heat, and high field magnetisation measurements.
Fitting exact diagonalisation and series expansion results to these data imply that
KTi(SO4)2·(H2O)is a long-sought experimental realization of the S = 1/2 Heisenberg
frustrated (J1 − J2) chain model in the dimerised regime of the phase diagram. The
anhydrous analogue of KTi(SO4)2·(H2O), KTi(SO4)2, was also investigated, and found
by magnetic neutron scattering to exemplify the S = 1/2 Heisenberg anisotropic triangular
lattice model in the 1D chain limit. The final two materials discussed are the
naturally occurring minerals volborthite and herbertsmithite, both thought to realise
the S = 1/2 Heisenberg kagome antiferromagnet model. Diffuse and inelastic magnetic
neutron scattering experiments, however, indicate that the kagome physics are partially
destroyed by defects in the former and lattice distortion in the latter. |
| Keywords: | Strongly correlated electrons magnetic susceptibility volborthite herbertsmithite antiferromagnetic model kagome physics |
| URI: | http://hdl.handle.net/1842/4920 |
| Appears in Collections: | Chemistry thesis and dissertation collection
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