This work develops a formalism to quantify the interaction among unpaired spins from the ground state spin topology. Magnetic systems where the spins are coupled through direct exchange and superexchange are chosen as references. Starting from a general Hamiltonian, an effective Hamiltonian is obtained in terms of spin density which is utilized to compute exchange coupling constants in magnetic systems executing direct exchange. The high-spin-low-spin energy gap, required to extract the coupling constant, is obtained through the broken symmetry approach within the framework of density functional theory. On the other hand, a perturbative approach is adopted to address the superexchange process. Spin transfer in between the sites in the exchange pathway is found to govern the magnetic nature of a molecule executing superexchange. The metal-ligand magnetic interaction is estimated using the second order perturbation energy for ligand to metal charge transfer and spin densities on the concerned sites. Using the present formalism, the total coupling constant in a superexchange process is also partitioned into the contributions from metal-ligand and metal-metal interactions. Sign and magnitude of the exchange coupling constants, derived through the present formalism, are found to be in parity with those obtained using the well-known spin projection technique. Moreover, in all of the cases, the ground state spin topology is found to complement the sign of coupling constants. Thus, the spin topology turns into a simple and logical means to interpret the nature of exchange interaction. The spin density representation in the present case resembles McConnell's spin density Hamiltonian and in turn validates it.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/ct2006506 | DOI Listing |
Chemistry
December 2024
Ulsan National Institute of Science and Technology, Chemistry, UNIST-gil 50, Bldg.108, Rm901-5, 44919, Ulsan, KOREA, REPUBLIC OF.
Nanographenes and polycyclic aromatic hydrocarbons, both finite forms of graphene, are promising organic semiconducting materials because their optoelectronic and magnetic properties can be modulated through precise control of their molecular peripheries. Several atomically precise edge structures have been prepared by bottom-up synthesis; however, no systematic elucidation of these edge topologies at the molecular level has been reported. Herein, we describe rationally designed modular syntheses of isomeric dibenzoixenes with diverse molecular peripheries, including cove, zigzag, bay, fjord, and gulf structured.
View Article and Find Full Text PDFNanoscale Horiz
December 2024
Electrical and Computer Engineering, The Grainger College of Engineering, University of Illinois Urbana-Champaign, Urbana, USA.
Antiferromagnetic materials have several unique properties, such as a vanishingly small net magnetization, which generates weak dipolar fields and makes them robust against perturbation from external magnetic fields and rapid magnetization dynamics, as dictated by the geometric mean of their exchange and anisotropy energies. However, experimental and theoretical techniques to detect and manipulate the antiferromagnetic order in a fully electrical manner must be developed to enable advanced spintronic devices with antiferromagnets as their active spin-dependent elements. Among the various antiferromagnetic materials, conducting antiferromagnets offer high electrical and thermal conductivities and strong electron-spin-phonon interactions.
View Article and Find Full Text PDFInorg Chem
December 2024
Felix Bloch Institute for Solid-State Physics, Leipzig University, Linnestrasse 5, 04103 Leipzig, Germany.
Two new dimorphic spin-1/2 quantum magnets, α- and β-CuO(VO)Cl, were synthesized via a chemical vapor transport method that emulates mineral formation in volcanic fumaroles. α-CuO(VO)Cl () is a pure vanadate analogue of the coparsite mineral characterized by [OCu] 1 single rods, whereas β-CuO(VO)Cl () adopts a new structure type with the [OCu] 2 layered topology. The thermal expansions of both and studied by high-temperature single-crystal X-ray diffraction are reported.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Toluca de Lerdo 50200, Mexico.
In this article, we provide details of the suite DensToolKit-v2, which consists of a set of cross-platform, optionally parallelized programs for analyzing the molecular electron density (ρ), as well as different fields and chemical indices derived from it. Notably, with this version, the user can compute the Non-Covalent Interaction index, the Density Overlap Regions Index, and fields related to single-spin-type molecular orbitals, such as the spin density. In addition, DensToolKit-v2 includes several programs for analyzing other less-known fields, such as the Density Matrix of order 1, the two-electron pair density function, and the Fourier transforms of these fields, that is, functionals in momentum space.
View Article and Find Full Text PDFRep Prog Phys
December 2024
Department of Physics, The University of Hong Kong, The University of Hong Kong, Pokfulam, Hong Kong, Hong Kong, 999077, HONG KONG.
Spinless systems exhibit unique topological characteristics compared to spinful ones, stemming from their distinct algebra. Without chiral interactions typically linked to spin, an intriguing yet unexplored interplay between topological and structural chirality may be anticipated. Here we discover spinless topological chiralities solely from structural chiralities that lie in the 3D spatial patterning of structureless units, exemplified using two types of twisted graphite systems.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!