Plasmonic Helical Nanoantenna As a Converter between Longitudinal Fields and Circularly Polarized Waves.

A wide variety of optical applications and techniques require control of light polarization. So far, the manipulation of light polarization relies on components capable of interchanging two polarization states of the transverse field of a propagating wave (e.g., linear to circular polarizations, and vice versa). Here, we demonstrate that an individual helical nanoantenna is capable of locally converting longitudinally oriented confined near-fields into a circularly polarized freely propagating wave, and vice versa. To this end, the nanoantenna is coupled to cylindrical surface plasmons bound to the top interface of a thin gold layer. Helices of constant and varying pitch lengths are experimentally investigated. The reciprocal conversion of an incoming circularly wave into diverging cylindrical surface plasmons is demonstrated as well. Interconnecting circularly polarized optical waves (carrying spin angular momentum) and longitudinal near-fields provides a new degree of freedom in light polarization control.

Stimulus-Responsive Plasmonic Chiral Signals of Gold Nanorods Organized on DNA Origami.

In response to environmental variations, living cells need to arrange the conformational changes of macromolecules to achieve the specific biofunctions. Inspired by natural molecular machines, artificial macromolecular assemblies with controllable nanostructures and environmentally responsive functions can be designed. By assembling macromolecular nanostructures with noble metal nanoparticles, environmental information could be significantly amplified and modulated. However, manufacturing dynamic plasmonic nanostructures that are efficiently responsive to different stimuli is still a challenging task. Here we demonstrate a stimulus-responsive plasmonic nanosystem based on DNA origami-organized gold nanorods (GNRs). L-shaped GNR dimers were assembled on rhombus-shaped DNA origami templates. The geometry and chiral signals of the GNR nanoarchitectures respond to multiple stimuli, including glutathione reduction, restriction enzyme action, pH change, or photoirradiation. While the glutathione reduction or restriction enzyme caused irreversible changes in the plasmonic circular dichroism (CD) signals, both pH and light irradiation triggered reversible changes in the plasmonic CD. Our system transduces external stimuli into conformational changes and circular dichroism responses in near-infrared (NIR) wavelengths. By this approach, programmable optical reporters for essential biological signals can be fabricated.

Accelerating Cellulose Nanocrystal Assembly into Chiral Nanostructures.

Cellulose nanocrystal (CNC) suspensions self-assembled into chiral nematic liquid crystals. This property has enabled the development of versatile optical materials with fascinating properties. Nevertheless, the scale-up production and commercial success of chiral nematic CNC superstructures face significant challenges. Fabrication of chiral nematic CNC nanostructures suffers from a ubiquitous pernicious trade-off between uniform chiral nematic structure and rapid self-assembly. Specifically, the chiral nematic assembly of CNCs is a time-consuming, spontaneous process that involves the organization of particles into ordered nanostructures as the solvent evaporates. This review is driven by the interest in accelerating chiral nematic CNC assembly and promoting a long-range oriented chiral nematic CNC superstructure. To start this review, the chirality origins of CNC and CNC aggregates are analyzed. This is followed by a summary of the recent advances in stimuli-accelerated chiral nematic CNC self-assembly procedures, including evaporation-induced self-assembly, continuous coating, vacuum-assisted self-assembly, and shear-induced CNC assembly under confinement. In particular, stimuli-induced unwinding, alignment, and relaxation of chiral nematic structures were highlighted, offering a significant link between the accelerated assembly approaches and uniform chiral nematic nanostructures. Ultimately, future opportunities and challenges for rapid chiral nematic CNC assembly are discussed for more innovative and exciting applications.

Gold nanoparticles with helical surface structure transformed from chiral molecules for SERS-active substrates preparation.

Surface-enhanced Raman scattering (SERS) technique has enlarged the application of Raman spectroscopy, and the most crucial problem is the exploration of SERS-active materials. In the paper, a SERS substrate made of helical gold nanoparticles by the directed synthesis of L-glutathione (L-GSH) was proposed. Because of the large surface specific area and the uneven conduction electrons distribution for sharp tips resulted from the complex concave surface and the symmetry breaking structure, The nanostructure has shown an impressive average enhancement factor (EF) of 2.95 × 105 under off-resonant condition. This phenomenon was explained by the experimental results and finite difference time domain (FDTD) method. Finally, the SERS substrates were used to detect thiram on pear with a limit of detection (LOD) of 0.62 mg/kg and R2 of 0.9772. The proposed SERS substrates suggest the potential application of chiral molecules such as amino acids, peptides et al. in the SERS-active materials fabrication.

Supramolecular chirality in self-assembled soft materials: regulation of chiral nanostructures and chiral functions.

Supramolecular chirality, which arises from the nonsymmetric spatial arrangement of components in the self-assembly systems, has gained great attention owing to its relation to the natural biological structures and the possible new functions in advanced materials. During the self-assembling process, both chiral and achiral components are possible to form chiral nanostructures. Therefore, it becomes an important issue how to fabricate these molecular components into chiral nanostructures. Furthermore, once the chiral nanostructure is obtained, will it show new functions that simple component molecule could not? In this research news, we report our recent development in the regulation of chiral nanostructures in soft gels or vesicle materials. We have further developed several new functions pertaining to the soft gel materials, which single chiral molecules could not perform, such as the chiroptical switch, chiral recognition and the asymmetry catalysis.