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Unconventional Thermal and Magnetic-Field-Driven Changes of a Bipartite Entanglement of a Mixed Spin-(1/2,S) Heisenberg Dimer with an Uniaxial Single-Ion Anisotropy
| Content Provider | MDPI |
|---|---|
| Author | Hana, Vargová Jozef, Strečka |
| Copyright Year | 2021 |
| Description | The concept of negativity is adapted in order to explore the quantum and thermal entanglement of the mixed spin-(1/2,S) Heisenberg dimers in presence of an external magnetic field. The mutual interplay between the spin size S, XXZ exchange and uniaxial single-ion anisotropy is thoroughly examined with a goal to tune the degree and thermal stability of the pairwise entanglement. It turns out that the antiferromagnetic spin-(1/2,S) Heisenberg dimers exhibit higher degree of entanglement and higher threshold temperature in comparison with their ferromagnetic counterparts when assuming the same set of model parameters. The increasing spin magnitude S accompanied with an easy-plane uniaxial single-ion anisotropy can enhance not only the thermal stability but simultaneously the degree of entanglement. It is additionally shown that the further enhancement of a bipartite entanglement can be achieved in the mixed spin-(1/2,S) Heisenberg dimers, involving half-odd-integer spins S. Under this condition the thermal negativity saturates at low-enough temperatures in its maximal value regardless of the magnitude of half-odd-integer spin S. The magnetic field induces consecutive discontinuous phase transitions in the mixed spin-(1/2,S) Heisenberg dimers with |
| Starting Page | 3096 |
| e-ISSN | 20794991 |
| DOI | 10.3390/nano11113096 |
| Journal | Nanomaterials |
| Issue Number | 11 |
| Volume Number | 11 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2021-11-16 |
| Access Restriction | Open |
| Subject Keyword | Nanomaterials Mathematical Physics Quantum Science and Technology Quantum and Thermal Entanglement Spin-(1/2,s) Heisenberg Dimer Exact Calculations Uniaxial Single-ion Anisotropy |
| Content Type | Text |
| Resource Type | Article |