Chirality represents a kind of symmetry breaking characterized by the noncoincidence of an object with its mirror image and has been attracting intense attention in a broad range of scientific areas. The recent realization of spin-orbit coupling in ultracold atomic gases provides a new perspective to study quantum states with chirality. In this Letter, we demonstrate that the combined effects of spin-orbit coupling and interatomic soft-core long-range interaction can induce an exotic supersolid phase in which the chiral symmetry is broken with spontaneous emergence of circulating particle current. This implies that a finite angular momentum can be generated with neither rotation nor effective magnetic field. The direction of the angular momentum can be altered by adjusting the strength of spin-orbit coupling or interatomic interaction. The predicted chiral supersolid phase can be experimentally observed in Rydberg-dressed Bose-Einstein condensates with spin-orbit coupling.
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http://dx.doi.org/10.1103/PhysRevLett.121.030404 | DOI Listing |
Inorg Chem
December 2024
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
The interplay between quantum effects from magnetic frustration, low-dimensionality, spin-orbit coupling, and crystal electric field in rare-earth materials leads to nontrivial ground states with unusual magnetic excitations. Here, we investigate YbTaO, which hosts a buckled square net of Yb ions with = 1/2 moments. The observed Curie-Weiss temperature is about -1 K, implying an antiferromagnetic coupling between the Yb moments.
View Article and Find Full Text PDFJ Phys Chem A
December 2024
Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, Alabama 35487-0336, United States.
Bond dissociation energies (BDEs) and spectroscopic parameters for the ground states of YbO and NoO were calculated at the Brueckner doubles (BD(T)) level and for NoO at the coupled cluster CCSD(T) level based on the closed-shell configurations Yb(4f)O(2p) and No(5f)O(2p). For YbO, the BD(T) BDE (3.93 eV) and vibrational frequency (686.
View Article and Find Full Text PDFPhotochem Photobiol
December 2024
Instituto de Química, Universidade de São Paulo, São Paulo, SP, Brazil.
Pyranoflavylium cations are synthetic analogues of pyranoanthocyanins, the much more color-stable compounds that are formed spontaneously from grape anthocyanins during the maturation of red wines. In the present work, our studies of the photophysical properties of pyranoanthocyanin analogues are extended to include nine pyranoflavylium cations substituted with one or two bromo and/or iodo heavy atoms. The room temperature fluorescence, 77 K fluorescence and phosphorescence, triplet formation in solution, and sensitized singlet oxygen formation, with excited state acidity suppressed by the addition of trifluoroacetic acid, are compared to those of similar pyranoflavylium cations that do not contain a heavy atom.
View Article and Find Full Text PDFChemphyschem
December 2024
Laboratoire de Chimie Quantique, Universit� de Strasbourg, Department of Chemistry, 4 rue Blaise Pascal, 67000, Strasbourg, FRANCE.
Recent, theoretical studies have shown that placing a spin-crossover ion in a field of radical ligands can induce local superpositions of local spin states (see Ref.[1,2]). This phenomenon, termed spinmerism, raises questions about its stability when spin-orbit coupling is included.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Institute of Theoretical Solid State Physics, Karlsruhe Institute of Technology, Kaiserstraße 12, 76131 Karlsruhe, Germany.
The formalism to calculate excited state properties from the GW-Bethe-Salpeter equation (BSE) method is introduced, providing convenient access to excited state absorption, excited state circular dichroism, and excited state optical rotation in the framework of the GW-BSE method. This is achieved using the second-order transition density, which can be obtained by solving a set of auxiliary equations similar to time-dependent density functional theory (TD-DFT). The proposed formulation therefore leads to no increase in the formal computational complexity when compared to the corresponding ground state properties.
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