Attention:The NSF Public Access Repository (PAR) system and access will be unavailable from 11:00 PM ET on Thursday, August 13 until 12:00 AM ET on Friday, August 14 due to maintenance. We apologize for the inconvenience.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


Title: Force Detection of Electromagnetic Chirality of Tightly Focused Laser Beams
We theoretically show that the optical chiral properties of tightly focused laser beams can be characterized by means of force detection. To measure the chiral properties of a beam of given handedness in the microscopic focal volume, we determine the photoinduced force exerted on a sharp tip, which is illuminated first by the beam of interest and second by an auxiliary beam of opposite handedness, in a sequential manner. We show that the difference between the force measurements is directly proportional to the chiral properties of the beam of interest. In particular, the gradient force difference Δ⟨Fgrad ,z⟩ is found to have exclusive correspondence to the time-averaged helicity density of the incident light, whereas the differential scattering force provides information about the spin angular momentum density of light. We further characterize and quantify the helicity-dependent Δ⟨Fgrad ,z⟩ using a Mie scattering formalism complemented with full wave simulations, underlining that the magnitude of the difference force is within an experimentally detectable range.  more » « less
Award ID(s):
1905582
PAR ID:
10347634
Author(s) / Creator(s):
; ;
Date Published:
Journal Name:
ACS Photonics
ISSN:
2330-4022
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; (, Physical Review Research)
    Chirality, or handedness, is a geometrical property denoting a lack of mirror symmetry. Chirality is ubiquitous in nature and is associated with the nonreciprocal interactions observed in complex systems ranging from biomolecules to topological materials. Here, we demonstrate that chiral arrangements of dipole-coupled atoms or molecules can facilitate the helicity-dependent superradiant emission of light. We show that the collective modes of these systems experience an emergent spin-orbit coupling that leads to chirality-dependent photon transport and nontrivial topological properties. These phenomena are fully described within the electric dipole approximation, resulting in very strong optical responses. Our results demonstrate an intimate connection between chirality, superradiance, and photon helicity and provide a comprehensive framework for studying electron transport dynamics in chiral molecules using cold atom quantum simulators. Published by the American Physical Society2024 
    more » « less
  2. ; ; ; ; ; ; ; ; ; (, Journal of the American Chemical Society)
    Creating new chiral molecular and macromolecular systems that can polarize the spin of electrons has the dual promise of both applications in spintronics and a fundamental understanding of their origins. Here, we put forward two optically active helical ladder dimers from perylene diimide-based twistacenes and helicenes. We detail a scalable method to separate the helices for each of these systems and methods to functionalize them with thiol groups that allow for self-assembled monolayer formation on metal surfaces. We probed these monolayers with conductive atomic force microscopy, revealing that they are highly conductive. If the substrate is magnetized, then the current we measure with conductive atomic force microscopy is controlled by the handedness of the helices used to form the monolayers. Furthermore, helices of the same handedness for either the twistacene or helicene (right-handed helices vs left-handed helices) produce high (or low) currents in devices with the same magnetization. Importantly, we find a correlation between the magnetic field dependence of the conductivity and the helicity of the molecules, suggesting a link between these two properties, independent of the sign of their electronic circular dichroism. 
    more » « less
  3. ; ; ; ; ; ; ; ; ; ; et al (, Advanced Functional Materials)
    Abstract Natural polymers, particularly plant‐derived nanocelluloses, self‐organize into hierarchical structures, enabling mechanical robustness, bright iridescence, emission, and polarized light reflection. These biophotonic properties are facilitated by the assembly of individual components during evaporation, such as cellulose nanocrystals (CNCs), which exhibit a left‐handed helical pitch in a chiral nematic state. This work demonstrates how optically active films with pre‐programmed opposite handedness (left or right) can be constructed via shear‐induced twisted printing with clockwise and counter‐clockwise shearing vectors. The resulting large‐area thin films are transparent yet exhibit pre‐determined mirror‐symmetrical optical activity, enabling the distinction of absorbed and emitted circularly polarized light. This processing method allows for sequential printing of thin and ultrathin films with twisted layered organization and on‐demand helicity. The complex light polarization behavior is due to step‐like changes in linear birefringence within each deposited layer and circular birefringence, different from that of conventional CNC films as revealed with Muller matrix analysis. Furthermore, intercalating an achiral organic dye into printed structures induces circularly polarized luminescence while preserving high transmittance and controlled handedness. These results suggest that twisted sequential printing can facilitate the construction of chiroptical metamaterials with tunable circular polarization, absorption, and emission for optical filters, encryption, photonic coatings, and chiral sensors. 
    more » « less
  4. ; ; (, Liquid Crystals)
    Azobenzene-based chiral dopants in cholesteric liquid crystals are of interest since the properties they induce in the liquid crystal could be tuned photochemically. Here, we use a substituted binaphthyl with a halogenated azobenzene as a chiral dopant to induce a photoswitchable cholesteric phase in the nematic 4-n-pentyl-4’-cyanobiphenyl. The azobenzene group chemically attached to the chiral dopant undergoes isomerization from trans to cis upon irradiation with green light (wavelength 535 nm), and from cis to trans upon irradiation with blue light (wavelength 450 nm). The transition between the two isomers causes helicity inversion of the cholesteric, with a left-handed trans isomer and a right-handed cis isomer. We report on the kinetics of photoisomerization of both processes (trans-to-cis and cis-to-trans) in the nematic host by following the pitch evolution over time. We show that the kinetic mechanism corresponds to a two-step process: a first-order isomerization followed by a second-order autocatalytic isomerization. This mechanism differs from the typical first-order kinetics for cis-to-trans or trans-to-cis isomerization in azobenzenes. The autocatalytic process is attributed to interactions between the chiral dopant and the nematic host. 
    more » « less
  5. (, Physica B: Condensed Matter)
    In the present work we theoretically analyze electroluminescence occurring in a biased single-molecule junction with a chiral bridge imitated by a helical chain. We show that optical transitions between electron states of the chiral linker may result in the emission of circular polarized light whose handedness depends on both direction of propagation and the polarity of the bias voltage provided that the coupling between the bridge sites is sufficiently strong. The mechanism controlling this specific light emission does not depend on the magnetic moments and spin–orbit interactions. It rather relies on the chiral properties of the bridge molecule and on the distribution of the bias voltage between the electrodes in the junction. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Text Encoded Conversion
  • XML
  • Save / Share this Record
  • Send to Email