Effect of Staggered Single-Ion Anisotropy in Non-linear Spin-1 Chains
ORAL · Invited
Abstract
Molecular ligands can be used to synthesize magnetic lattices that are difficult to create using inorganic materials. Examples include non-linear antiferromagnetic chains, in which the orientation of the local environment of the magnetic ion changes from site to site. Spin-1/2 non-linear chains exhibit additional terms in their Hamiltonians as compared to conventional magnets, including non-trivial staggered g-tensors and Dzyalonshinskii-Moriya interactions. On application of an external magnetic field, these energy scales can give rise to staggered fields, field-dependent energy gaps and low-temperature excitation spectra containing both breather and soliton modes [1–3].
Spin-1 AFM chains are known to adopt ground states that differ fundamentally from their spin-1/2 counterparts, an example being the Haldane-gapped phase. Here, we present magnetometry, muon-spin rotation and neutron-scattering data on the newly synthesized spin-1 two-fold staggered chain Ni(pyrimidine)(NO3)2(H2O)2, the four-fold chiral chain [Ni(pyrimidine)(H2O)4]SO4, and the diamond-lattice material NiCl2(pyrimidine)2 [4,5]. The alternating single-ion-anisotropy axis accompanying the alternating local g-tensors, as well as competition between the anisotropy and the exchange along the pyrimidine molecules adds a different level of complexity to these novel quantum magnets.
[1] D. C. Dender et al., Phys. Rev. Lett. 79, 1750 (1997)
[2] S. A. Zvyagin et al., Phys. Rev. Lett. 93, 027201 (2004)
[3] J. Liu et al., Phys. Rev. Lett. 122, 57207 (2019)
[4] S. Vaidya et al., arXiv:2405.15623 (2024)
[5] S. Vaidya et al., arXiv:2407.17894 (2024)
Spin-1 AFM chains are known to adopt ground states that differ fundamentally from their spin-1/2 counterparts, an example being the Haldane-gapped phase. Here, we present magnetometry, muon-spin rotation and neutron-scattering data on the newly synthesized spin-1 two-fold staggered chain Ni(pyrimidine)(NO3)2(H2O)2, the four-fold chiral chain [Ni(pyrimidine)(H2O)4]SO4, and the diamond-lattice material NiCl2(pyrimidine)2 [4,5]. The alternating single-ion-anisotropy axis accompanying the alternating local g-tensors, as well as competition between the anisotropy and the exchange along the pyrimidine molecules adds a different level of complexity to these novel quantum magnets.
[1] D. C. Dender et al., Phys. Rev. Lett. 79, 1750 (1997)
[2] S. A. Zvyagin et al., Phys. Rev. Lett. 93, 027201 (2004)
[3] J. Liu et al., Phys. Rev. Lett. 122, 57207 (2019)
[4] S. Vaidya et al., arXiv:2405.15623 (2024)
[5] S. Vaidya et al., arXiv:2407.17894 (2024)
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Publication: [4] Pseudo-easy-axis anisotropy in antiferromagnetic S = 1 diamond-lattice systems
S. Vaidya, A. Hernández-Melián, J. P. Tidey, S. P. M. Curley, S. Sharma, P. Manuel, C. Wang, G. L. Hannaford, S. J. Blundell, Z. E. Manson, J. L. Manson, J. Singleton, T. Lancaster, R. D. Johnson, P. A. Goddard, arXiv:2405.15623 (2024)
[5] Magnetic properties of a staggered S = 1 chain with an alternating single-ion anisotropy direction
S. Vaidya, S. P. M. Curley, P. Manuel, J. Ross Stewart, M. Duc Le, T. Shiroka, S. J. Blundell, K. A. Wheeler, Z. E. Manson, J. L. Manson, J. Singleton, T. Lancaster, R. D. Johnson, P. A. Goddard,
arXiv:2407.17894 (2024)
Presenters
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Paul A Goddard
- University of Warwick