WoS İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/394
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Article Citation - WoS: 4Citation - Scopus: 3Multifaceted Effects of the Dielectric Component Within Plasmon-Assisted Light-Emitting Structures(American Chemical Society, 2025-10-23) Kulakovich, O.; Muravitskaya, A.; Ramanenka, A.; Efimova, T.; Krukov, V.; Mutlugün, E.; Gaponenko, S.Plasmon-enhanced photoluminescence of molecular probes and semiconductor nanocrystals is a rapidly developing field that promises enhanced sensitivity in chemical and biomedical analyses, as well as higher efficiency of light-emitting devices and single-photon sources. The dielectric component, or spacer, is typically used to control the distance between the emitter and the plasmonic nanoparticle in order to decrease undesirable nonradiative energy transfer to the metal and achieve high enhancement efficiency. While most research focuses on the shape and organization of the plasmonic nanoparticles, less attention is given to the role of the dielectric component in plasmon-enhancing structures. Meanwhile, the dielectric shell or environment critically modulates near-field enhancement, far-field scattering, charge and energy exchange between the emitter and the plasmonic structure, and the general environmental stability of the structure. In this review, we discuss all mentioned topics and therefore consider both the optical and chemical influence of the widely used spacers and dielectric layers on plasmon-enhanced photoluminescence efficiency. Investigating the role of individual components in plasmon-assisted light-emitting structures is critical for optimizing device performance and for advancing the integration of plasmonic architectures in optoelectronic and sensing applications. This review challenges the passive interpretation of dielectrics, revealing them as one of the key players in plasmonic structures, mediating field enhancement, emission dynamics, and chemical stability simultaneously. © 2025 American Chemical SocietyArticle Citation - Scopus: 1Labyrinthine Microstructures With a High Dipole Moment Boron Complex for Molecular Physically Unclonable Functions(American Chemical Society, 2025-10-29) Yıldız, T.A.; Kiremitler, N.B.; Kayacı, N.; Kalay, M.; Özcan, E.; Deneme, I.; Usta, H.The design and development of novel molecular-physically unclonable functions (PUFs) with advanced encoding characteristics and ease of fabrication have recently attracted attention in cryptography, secure authentication, and anticounterfeiting. Here, we report the development of a new high dipole-moment small molecule, InIm-BF<inf>2</inf>, a difluoroborate complex of an indolyl-imine ligand, and the fabrication of unique labyrinthine patterns through a facile two-step thin film process under ambient conditions. The new molecule has a dipolar, coplanar π-backbone and arranges in the solid state with antisymmetric cofacial π-stackings (3.86 Å). These properties, along with short C–H···π contacts (2.74–2.88 Å) and nonclassical C–H···F hydrogen bonds (2.47–2.51 Å) (23.4% and 11.5% of the Hirshfeld surfaces, respectively), drive the formation of amorphous molecular PUF patterns with disordered, short-range interactions. Spin-coating followed by thermal annealing at a moderate temperature produces nanoscopic molecular thin films with intricate labyrinthine patterns. These patterns, characterized by interconnected, irregularly shaped, micron-sized (≈50–100 μm) features, exhibit excellent PUF characteristics, verified through advanced image analysis and computational algorithms. Unlike randomly positioned isolated features in classical binarized keys, the interconnected labyrinthine patterns possess rich entropy and complex features, directly authenticated via deep-learning methodologies. Our work not only demonstrates a facile, promising approach to fabricating unique high-entropy PUF patterns but also provides critical insights into designing advanced molecular materials for next-generation security applications. © 2025 The Authors. Published by American Chemical Society