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Dynamical and self-trapping properties of two-dimensional (2D) binary mixtures of Bose-Einstein condensates in cross-combined lattices, consisting of a one-dimensional (1D) linear optical lattice (LOL) in the x direction for the first component and a 1D nonlinear optical lattice (NOL) in the y direction for the second component, are analytically and numerically investigated. The existence and stability of 2D binary matter wave solitons in these settings are demonstrated both by variational analysis and by direct numerical integration of the coupled Gross-Pitaevskii equations. We find that in the absence of the NOL, binary solitons, stabilized by the action of the 1D LOL and by the attractive intercomponent interaction, can freely move in the y direction. In the presence of the NOL, we find, quite remarkably, the existence of threshold curves in the parameter space separating regions where solitons can move from regions where the solitons become dynamically self-trapped. The mechanism underlying the dynamical self-trapping phenomenon (DSTP) is qualitatively understood in terms of a dynamical barrier induced by the NOL, similar to the Peirls-Nabarro barrier of solitons in discrete lattices. DSTP is numerically demonstrated for binary solitons that are put in motion both by phase imprinting and by the action of external potentials applied in the y direction. In the latter case, we show that the trapping action of the NOL allows one to maintain a 2D binary soliton at rest in a nonequilibrium position of a parabolic trap or to prevent it from falling under the action of gravity. Possible applications of the results are also briefly discussed.
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http://dx.doi.org/10.1103/PhysRevE.108.054218 | DOI Listing |
Nat Commun
August 2025
School of Materials Science and Engineering, Peking University, Beijing, China.
An emerging class of two-dimensional semiconductor materials, metal-organic chalcogenolates (MOCs), have garnered significant attention due to the strong excitonic effects arising from their intrinsic soft, hybrid multiquantum-well structures. However, modifying excitonic transitions that strongly couple to the argentophilic networks and constructing their structure-property relationships in MOCs remain daunting challenges. Here, we use silver phenylselenolate (AgSePh) as a model system to manipulate excitonic behavior and uncover the fundamental photophysical mechanisms through pressure engineering.
View Article and Find Full Text PDFLight Sci Appl
July 2025
Henan Key Laboratory of Diamond Optoelectronic Materials and Devices, Key Laboratory of Material Physics Ministry of Education, School of Physics and Key Laboratory of Zhongyuan Light, Zhengzhou University, Zhengzhou, China.
Size-scalable X-ray scintillators with high transparency and robust photon yield allow for imaging large objects with greater precision and detail. Solution-processable scintillators, typically crafted from quantum dots (QDs), are promising candidates for highly efficient scintillation applications. However, the restricted size and low transparency in QD-based scintillators lead to less efficient X-ray imaging for large objects requiring high resolution.
View Article and Find Full Text PDFAdv Mater
July 2025
Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of Queensland St Lucia, Queensland, 4072, Australia.
2D organic semiconductors are widely considered superior photocatalysts due to their large basal planes, which host abundant and tunable reaction sites. However, here, it is discovered that these basal planes can be pseudo-inert, fundamentally challenging conventional design strategies that assume uniform activity on the surface of 2D organic semiconductors. Using 2D potassium-poly (heptazine imide) (KPHI) for hydrogen peroxide photocatalysis as a model, it is demonstrated that the pseudo-inertness of basal planes stems from preferential exciton transport to edges, instead of interlayer transport in highly ordered structures.
View Article and Find Full Text PDFJ Am Chem Soc
May 2025
State Key Laboratory of Extreme Photonics and Instrumentation, Zhejiang Key Laboratory of Excited-State Energy Conversion and Energy Storage, Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310058, China.
White-light emission (WLE) with tunable chromaticity and correlated color temperature (CCT) is critical for lighting, display, and sensing applications. While recent two-dimensional (2D) lead halide perovskites have emerged as promising single-component WLE materials, their application is hindered by constrained and low CCT due to dominant localized exciton (LE) emission. Here, we report a dynamic exciton polaron mechanism in ⟨100⟩-oriented 2D lead bromides, (CHN)PbBr ( = 5, 7, 9, 11), enabling intrinsic dual-mode WLE with widely tunable CCT.
View Article and Find Full Text PDFJ Phys Chem Lett
May 2025
Departamento de Ciencia y Tecnologia, Universidad Nacional de Quilmes/CONICET, B1876BXD Bernal, Argentina.
The synthesis of novel carbon nanostructures with unique topologies expands the landscape of organic molecules, introducing new chemical properties and potential applications. Carbon nanorings, composed of cyclic paraphenylene (CPP) chains, serve as a versatile scaffold for designing materials with unique molecular architectures that impact their optical properties and photoinduced dynamics. These new topologies alter the balance between competing π-conjugation effects, high bending strain energies, and steric hindrances imposed by the rearrangement of their cyclic structures.
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