Magnetoelectric coupling on fused azulene oligomers
The global magnetic phase diagram for fused azulene oligomers is obtained by using a fermionic Hubbard model, which is an intermediate between the molecular Pariser-Parr-Pople empiric Hamiltonian and the spin-1/2 antiferromagnetic Heisenberg model. We employ the density matrix renormalization group...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2022 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/214472 |
| Acceso en línea: | http://hdl.handle.net/11336/214472 |
| Access Level: | acceso abierto |
| Palabra clave: | Magnetic phase transitions Quantum phase transitions Molecular magnets https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
| Sumario: | The global magnetic phase diagram for fused azulene oligomers is obtained by using a fermionic Hubbard model, which is an intermediate between the molecular Pariser-Parr-Pople empiric Hamiltonian and the spin-1/2 antiferromagnetic Heisenberg model. We employ the density matrix renormalization group (DMRG) approach to explore the ground state properties of azulene-like molecules as a function of the electronic correlation and the oligomer size. It is shown that, depending on the length of the oligomer, fused azulene transitions from a singlet (S=0) to a higher-spin (S=1,2) ground state. Near the quantum magnetic phase transition the electric dipole moment, present on fused azulene molecules, couples with the magnetic moment leading to a divergent magnetoelectric susceptibility at the boundary lines of the magnetic phase diagram. These spontaneous electric and magnetic polarizations, together with the magnetoelectric coupling between them, indeed corroborate that these fused azulene oligomers can be viewed as a purely organic multiferroic material, being a magnetoelectric molecule. |
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