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Chiral plasmonic nanomaterials─with their significant applications in protein detection, drug screening, and enantioselective sensing─necessitate an industrialized fabrication procedure to enhance their commercial viability. However, the prevailing manufacturing of chiral plasmonic nanoparticles and assemblies heavily leans on manual intervention, causing time-consuming and quality-inconsistent concerns. Here, we develop an automated, continuous mechanical synthesis system that consistently sprays metal nanowires to create chiroplasmonic assemblies: a macroscopic twisted layered structure comprising equivalent linear birefringence layers, approximate linear polarizer layers, and a precise angular offset between them. Utilizing the synthesis-with-automation system, we scale up the production of chiral plasmonic films, generating high optical asymmetry (-factor, with the order of 10) across a broadband ranging from ultraviolet to near-infrared wavelengths. We further introduce the portable chiral sensing, expanding plasmonic assemblies into flexible materials and integrating them with wearable real-time display devices. Our mechanically driven, continuous synthesis of chiral plasmonic structures presents an intriguing pathway to facilitate functional chiral structures toward practice.
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http://dx.doi.org/10.1021/jacs.4c09671 | DOI Listing |
Nanophotonics
August 2025
Departament de Física de la Matèria Condensada, Universitat de Barcelona, 08028 Barcelona, Spain.
We present a systematic investigation of the optical response to circularly polarized illumination in twisted stacked plasmonic nanostructures. The system consists in two identical, parallel gold triskelia, centrally aligned and rotated at a certain angle relative to each other. Sample fabrication was accomplished through a novel multilevel high-resolution electron beam lithography.
View Article and Find Full Text PDFNat Commun
August 2025
Zhejiang Key Laboratory of Micro-Nano Quantum Chips and Quantum Control, State Key Laboratory for Extreme Photonics and Instrumentation, School of Physics, Zhejiang University, Hangzhou, China.
Chiral coupling offers alternative avenues for controlling and exploiting light-matter interactions. We demonstrate that chiral coupling can be utilized to achieve unidirectional perfect absorption. In our experiments, chiral magnon-photon coupling is realized by coupling the magnon modes in yttrium iron garnet (YIG) spheres with spin-momentum-locked waveguide modes supported by spoof surface plasmon polaritons (SSPPs).
View Article and Find Full Text PDFSpontaneous parametric down conversion (SPDC) has proven to be a robust and prominent method for creating non-classical light sources of entangled single-photon pairs. However, such sources suffer from low efficiency due to the inherent weakness of the SPDC process. Moreover, there is no control of polarization in the generated photons.
View Article and Find Full Text PDFACS Photonics
August 2025
Department of Chemistry and The Photonics Center, Boston University, Boston, MA 02215, USA.
Electronic absorption bands of important biomolecules and pharmaceutical compounds lie in the ultraviolet (UV) between 180 nm and 280 nm and thus in a spectral range that does not overlap with the localized surface plasmon resonances (LSPRs) of conventional gold (Au) or silver (Ag) nanoantennas. Aluminum (Al) nanostructures support resonances in the UV, and there is significant interest in utilizing UV-resonant nanostructured Al substrates for enhancing the sensitivity of chiroptical spectroscopies, such as circular dichroism (CD). In this study, we compare the CD of a chiral molecular film on Al and Ag substrates and evaluate the role of inherent and induced absorptive CD as well as of scattering CD in the UV.
View Article and Find Full Text PDFACS Nano
September 2025
Guangdong Basic Research Center of Excellence for Aggregate Science, School of Science and Engineering, The Chinese University of Hong Kong, Shenzhen, Guangdong 518172, China.
Exploring switching strategies for intrinsically chiral plasmonic nanoparticles is crucial for unlocking their potential in the dynamic manipulation of light polarization states. Conjugated polymers, such as polyaniline (PANI), represent highly promising material candidates for this pursuit, owing to their combination of intrinsic structural flexibility, tunable optical characteristics, and multistimuli responsiveness. Herein, we demonstrate chiroptical switching on PANI-encapsulated chiral gold nanorods (cAuNRs) by controlling proton doping of PANI, and reveal that the morphology of PANI within the nanogaps of cAuNRs results in abnormal spectral shifting, which is in contrast with those in previous studies.
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