RESUMEN
Second-order optical nonlinearity is the essential concept for realizing modern technologies of optical wavelength conversion. The emerging helical polarization fluid, dubbed helielectric nematic, now makes it possible to design and easily fabricate various polarization structures and control their optical responses. The matter family is demonstrated as an ideal liquid platform for nonlinear optical conversion and amplification with electric-reconfigurable tunability. We here develop a universal phase matching theory and reveal a nonclassic chirality-sensitive phase-matching condition in the polarization helices through both the numerical calculation and the experimental validations. The nonlinear optical amplification can be dramatically modulated with a contrast ratio of >100:1 by an in-plane electric field. Furthermore, we employ the director relaxation under electric fields coupled with nonlinear optical simulation to clarify the topology-light interactions.
RESUMEN
Recently, a type of ferroelectric nematic fluid has been discovered in liquid crystals in which the molecular polar nature at molecule level is amplified to macroscopic scales through a ferroelectric packing of rod-shaped molecules. Here, we report on the experimental proof of a polar chiral liquid matter state, dubbed helielectric nematic, stabilized by the local polar ordering coupled to the chiral helicity. This helielectric structure carries the polar vector rotating helically, analogous to the magnetic counterpart of helimagnet. The helielectric state can be retained down to room temperature and demonstrates gigantic dielectric and nonlinear optical responses. This matter state opens a new chapter for developing the diverse polar liquid crystal devices.
RESUMEN
By analogy with spin waves in ferromagnetic systems, the polarization (or dipole) wave is the electric counterpart that remains elusive. Here, we discover that the helielectricity, i.e. a polarization field with helicoidal helices that corresponds to a quasi-layered chiral nematic environment, causes a spontaneous formation of large-scale polarization waves in the form of the sinusoidal function. Both experimental and theoretical analyses reveal that the polarization ordering over a threshold polarization strength violates the inherent periodicity of the polarization helices, thus penalizing the compression energy. It drives a second-order structural transition to a periodically modulated polarization wave state. The roles of chirality and confinement condition are discussed.