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Register a new userCircular Dichroism in Rotating Particles
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Light interaction with rotating nanostructures gives rise to phenemona as varied as optical torques and quantum friction. Here we reveal that circular dichroism of rotating optically-isotropic particles has an unexpectedly strong dependence on their internal geometry. In particular, nanorings and nanocrosses exhibit a splitting of $2Omega$ in the particle optical resonances, while compact particles display weak circular dichroism at low rotation frequency $Omega$, but a strong circular dichroism at high $Omega$. We base our findings on a quantum-mechanical description of the polarizability of rotating particles, which has not been rigorously addressed so far. Specifically, we use the random-phase approximation and populate the particle electronic states according to the principle that they are thermally equilibrated in the rotating frame. We further provide insight into the rotational superradience effect and the ensuing optical gain, originating in population inversion as regarded from the lab frame, in which the particle is out of equilibrium. Surprisingly, we find the optical frequency cutoff for superradiance to deviate from the rotation frequency $Omega$. Our results unveil a rich, unexplored phenomenology of light interaction with rotating objects.
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Circular dichroism (CD), induced by chirality, is an important tool for manipulating light or for characterizing morphology of molecules, proteins, crystals and nano-structures. CD is manifested over a wide size-range, from molecules to crystals or large nanostructures. Being a weak phenomenon (small fraction of absorption), CD is routinely measured on macroscopic amount of matter in solution, crystals, or arrays of fabricated meta-particles. These measurements mask the sensitivity of CD to small structural variation in nano-objects. Recently, several groups reported on chiroptical effects in individual nanoscale objects: Some, using near-field microscopy, where the tip-object interaction requires consideration. Some, using dark field scattering on large objects, and others by monitoring the fluorescence of individual chiral molecules. Here, we report on the direct observation of CD in individual nano-objects by far field extinction microscopy. CD measurements of both chiral shaped nanostructures (Gammadions) and nanocrystals (HgS) with chiral lattice structure are reported.
Topological insulators are a new phase of matter that exhibits exotic surface electronic properties. Determining the spin texture of this class of material is of paramount importance for both fundamental understanding of its topological order and future spin-based applications. In this article, we review the recent experimental and theoretical studies on the differential coupling of left- versus right-circularly polarized light to the topological surface states in angle-resolved photoemission spectroscopy. These studies have shown that the polarization of light and the experimental geometry plays a very important role in both photocurrent intensity and spin polarization of photoelectrons emitted from the topological surface states. A general photoemission matrix element calculation with spin-orbit coupling can quantitatively explain the observations and is also applicable to topologically trivial systems. These experimental and theoretical investigations suggest that optical excitation with circularly polarized light is a promising route towards mapping the spin-orbit texture and manipulating the spin orientation in topological and other spin-orbit coupled materials.
The helical Dirac fermions at the surface of topological insulators show a strong circular dichroism which has been explained as being due to either the initial-state spin angular momentum, the initial-state orbital angular momentum, or the handedness of the experimental setup. All of these interpretations conflict with our data from Bi2Te3 which depend on the photon energy and show several sign changes. Our one-step photoemission calculations coupled to ab initio theory confirm the sign change and assign the dichroism to a final-state effect. The spin polarization of the photoelectrons, instead, remains a reliable probe for the spin in the initial state.
We theoretically investigate the optical activity of three dimensional Dirac semimetals (DSMs) using circular dichroism (CD). We show that DSMs in the presence of a magnetic field in any one of the mirror-symmetric planes of the materials exhibit a notable dichroic behavior. In particular, for different orientations of the light field with respect to the mirror-symmetric plane, the CD in type-II DSMs can detect the presence of mirror anomaly by showing sharply distinct patterns at the mirror-symmetric angle. Interestingly, CD can also distinguish type-II DSMs having only one Dirac point at a time-reversal invariant momentum from type-I DSMs with a pair of Dirac points on the rotation axis of the crystals.
Topological insulators have been successfully identified by spin-resolved photoemission but the spin polarization remained low (~20%). We show for Bi2Te3 that the in-gap surface state is much closer to full spin polarization with measured values reaching 80% at the Fermi level. When hybridizing with the bulk it remains highly spin polarized which may explain recent unusual quantum interference results on Bi2Se3. The topological surface state shows a large circular dichroism in the photoelectron angle distribution with an asymmetry of ~20% the sign of which corresponds to that of the measured spin.
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