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The generation of cold molecules is an important topic in the field of cold atoms and molecules and has received relevant advanced research attention in ultracold chemistry, quantum computation, and quantum metrology. With a high atomic phase space density, optical dipole traps have been widely used to prepare, trap, and study cold molecules. In this work, Rb2 molecules were photoassociated in a magneto-optical trap to obtain a precise rovibrational spectrum, which provided accurate numerical references for the realization of multiple frequency photoassociation. By meeting the harsh requirements of photoassociation in optical dipole traps, the cold molecule photoassociation process was well explored, and different photoassociation resonances were simultaneously addressed in a single optical dipole trap. This method can be universally extended to simultaneously photoassociate cold molecules with different internal states or atomic species in a single optical dipole trap, thus advancing generous cold molecule studies such as cold molecule collision dynamics.
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http://dx.doi.org/10.1063/5.0226482 | DOI Listing |
J Chem Theory Comput
September 2025
International Center for Quantum and Molecular Structures, Faculty of Physics, Shanghai University, Shanghai 200444, China.
The representation of the electronic structure of benzene is important for understanding the properties of planar and monocyclic organic carbon compounds. Resonant Kekulé and conjugated structures based on localized and delocalized electronic theories, respectively, can be used to depict the ground state of benzene; however, depictions of its electrons vibrating in the excited states remain to be clarified. This paper presents a novel algorithm for exploring the three lowest lying vertically singlet excited states of benzene, focusing on the electronic excitations between occupied π and unoccupied π* orbitals.
View Article and Find Full Text PDFNanoscale Horiz
September 2025
Theoretical Chemical Physics Group, Research Institute for Materials Science and Engineering, University of Mons, 20 Place du Parc, Mons B-7000, Belgium.
Two-photon spontaneous emission (TPSE) is a second-order quantum process with promising applications in quantum optics that remains largely unexplored in molecular systems, which are usually very inefficient emitters. In this work, we model the first molecular two-photon emitters and establish the design rules, highlighting their differences from those governing two-photon absorbers. Using both time-dependent density functional theory and Pariser-Parr-Pople calculations, we calculate TPSE in three π-conjugated molecules and identify a dominant pathway.
View Article and Find Full Text PDFSci Adv
September 2025
Australian Research Council Centre of Excellence for Transformative Meta-Optical Systems, Department of Electronic Materials Engineering, Research School of Physics, The Australian National University, Canberra, ACT 2600, Australia.
Surface-emitting lasers featuring optical bound states in the continuum (BICs) have recently emerged as a promising alternative to vertical cavity surface-emitting lasers. However, structural damage caused by top-down fabrication processes remains as a major obstacle that limits device performance. Here, we overcome this bottleneck by demonstrating surface-emitting quasi-BIC lasers fabricated with a bottom-up, etching-free process.
View Article and Find Full Text PDFLight Sci Appl
September 2025
Department of Materials Science and Engineering, Centre for Functional Photonics, and Hong Kong Branch of National Precious Metals Material Engineering Research Centre, City University of Hong Kong, Hong Kong, China.
Observation of the second-harmonic generation (SHG) from subwavelength metallic structures is often hindered by the interrelations of higher-order multipolar contributions. In particular, the magnetic Lorentz contribution to SHG is often neglected due to the ineffective magnetic field enhancement in electrically resonant structures. Here, we demonstrate a strong Lorentz-driven SHG output at the plasmon-induced magnetic dipolar resonance in inversion-symmetry-broken plasmonic nanocavities.
View Article and Find Full Text PDFAnal Chem
September 2025
Interdisciplinary Laboratories for Advanced Materials Physics (i-LAMP) & Dipartimento di Matematica e Fisica, Università Cattolica del Sacro Cuore, via della Garzetta 48, 25133 Brescia, Italy.
Optical recognition and identification of nanoplastics such as polystyrene nanobeads (PSbs), a widely used polymer and an actual source of environmental pollution, is a challenging task relying on knowledge of the PSbs' refractive index (RI) and its relation to the PSbs' morphology. This is, however, lacking for PSbs' sizes lower than 1 μm. Here, we bridge this gap by measuring UV-vis spectra of PSbs deposited on a sapphire substrate via spin coating and by connecting the experimental data to the RI, PSbs' morphology, and optical transitions through a new optical model based on the Mie theory.
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