Three dimensional (3D) Dirac semimetals are 3D analogue of graphene, which display Dirac points with linear dispersion in k-space, stabilized by crystal symmetry. Cd3As2 and Na3Bi were predicted to be 3D Dirac semimetals and were subsequently demonst
rated by photoemission experiments. As unveiled by transport measurements, several exotic phases, such as Weyl semimetals, topological insulators, and topological superconductors, can be deduced by breaking time reversal or inversion symmetry. Here, we reported a facile and scalable chemical vapor deposition method to fabricate high-quality Dirac semimetal Cd3As2 microbelts, they have shown ultrahigh mobility up to 1.15*10^5 cm^2/V s and pronounced Shubnikov-de Haas oscillations. Such extraordinary features are attributed to the suppression of electron backscattering. This research opens a new avenue for the scalable fabrication of Cd3As2 materials towards exciting electronic applications of 3D Dirac semimetals.
Pseudospin, an additional degree of freedom inherent in graphene, plays a key role in understanding many fundamental phenomena such as the anomalous quantum Hall effect, electron chirality and Klein paradox. Unlike the electron spin, the pseudospin w
as traditionally considered as an unmeasurable quantity, immune to Stern-Gerlach-type experiments. Recently, however, it has been suggested that graphene pseudospin is a real angular momentum that might manifest itself as an observable quantity, but so far direct tests of such a momentum remained unfruitful. Here, by selective excitation of two sublattices of an artificial photonic graphene, we demonstrate pseudospin-mediated vortex generation and topological charge flipping in otherwise uniform optical beams with Bloch momentum traversing through the Dirac points. Corroborated by numerical solutions of the linear massless Dirac-Weyl equation, we show that pseudospin can turn into orbital angular momentum completely, thus upholding the belief that pseudospin is not merely for theoretical elegance but rather physically measurable.
In this work, we demonstrate that the nonlinear response of certain soft-matter systems can be tailored at will by appropriately engineering their optical polarizability. In particular, we deliberately synthesize stable colloidal suspensions with neg
ative polarizabilities, and observe for the first time robust propagation and enhanced transmission of self-trapped light over long distances that would have been otherwise impossible in conventional suspensions with positive polarizabilities. What greatly facilitates this behavior is an induced saturable nonlinear optical response introduced by the thermodynamic properties of these colloidal systems. This in turn leads to a substantial reduction in scattering via self-activated transparency effects. Our results may open up new opportunities in developing soft-matter systems with tunable optical nonlinearities.
