A route to produce novel three-dimensional structures in thin films is demonstrated. Such structures are most difficult to produce in a simple manner without the use of multiple fabrication steps. Here, we show the generation of 3-D cage-type structures using a combination of electrohydrodynamic instabilities and dewetting in a polymer/polymer/air trilayer. Removal of one of the components by use of a selective solvent or by degradation of one of the components reveals the formation of a three-dimensional structure, where one polymer is encased in the other. Thus, by coupling an external field with a surface field inherent to the polymers, a novel fabrication strategy is shown that has clear applications in microfluidics and microelectromechanical systems with extensions to patterned surfaces and structured fluids, like block copolymers.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/la052954e | DOI Listing |
Phys Chem Chem Phys
January 2025
Institute of Inorganic Chemistry, Slovak Academy of Sciences, Dúbravská cesta 9, SK-84536 Bratislava, Slovakia.
The solvent effect on the indirect J(M-P) spin-spin coupling constant in phosphine selenoether -substituted acenaphthene complexes LMCl is studied at the PP86 level of nonrelativistic and four-component relativistic density functional theory. Depending on the metal, the solvent effect can amount to as much as 50% or more of the total -value. This explains the previously found disagreement between the J(Hg-P) coupling in LHgCl, observed experimentally and calculated without considering solvent effects.
View Article and Find Full Text PDFFluorescent antennas (FAs) exhibit considerable promise in optical wireless communication (OWC), primarily due to their advantages over conventional optical systems in terms of optical gain and field of view (FoV). This paper presents a COMSOL-based model designed to optimize external light-concentrating structures for FAs, with its accuracy validated through both qualitative and quantitative comparisons. Leveraging refractive index modulation and the conservation of optical étendue, two distinct light-concentrating structures are developed.
View Article and Find Full Text PDFFilm-coupled plasmonic resonators offer efficient platforms for light enhancement due to the excitation of gap surface plasmons (GSPs) at metal-insulator-metal interfaces, where electromagnetic energy is stored within the spacer. In applications like biosensing and spontaneous emission control, spatial overlap between the target molecule and plasmonic hotspots is essential. Here, we propose utilizing the controllable, efficient light enhancement capabilities of a specifically designed GSP disk resonator for biosensing and spontaneous emission enhancement.
View Article and Find Full Text PDFWe analyze the single-photon band structure and the transport of a single photon in a one-dimensional coupled-spinning-resonator chain. The time-reversal symmetry of the resonators chain is broken by the spinning of the resonators, instead of external or synthetic magnetic field. Two nonreciprocal single-photon band gaps can be obtained in the coupled-spinning-resonator chain, whose width depends on the angular velocity of the spinning resonator.
View Article and Find Full Text PDFJ Phys Condens Matter
January 2025
School of Physics Science and Engineering, Tongji University, siping road, Shanghai, 200092, CHINA.
Hybrid magnonics has attracted extensive attention for its potential applications in quantum information processing, especially following the discovery of strong coupling in magnon-magnon hybrid systems. In this paper, we studied the coupling phenomena between the left-handed (LH) and right-handed (RH) magnon modes in synthetic antiferromagnets (SAFs) with a tilted perpendicular magnetic anisotropy (PMA). By tilting the PMA at a certain angle from the film normal, we achieved strong magnon-magnon coupling without the need for an external magnetic field.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!