Vanishing of interband light absorption in a persistent spin helix state
Spin-orbit coupling plays an important role in various properties of very different materials. Moreover efforts are underway to control the degree and quality of spin-orbit coupling in materials with a concomitant control of transport properties. We calculate the frequency dependent optical conductivity in systems with both Rashba and Dresselhaus spin-orbit coupling. We find that when the linear Dresselhaus spin-orbit coupling is tuned to be equal to the Rashba spin-orbit coupling, the interband optical conductivity disappears. This is taken to be the signature of the recovery of SU(2) symmetry. The presence of the cubic Dresselhaus spin-orbit coupling modifies the dispersion relation of the charge carriers and the velocity operator. Thus the conductivity is modified, but the interband contribution remains suppressed at most but not all photon energies for a cubic coupling of reasonable magnitude. Hence, such a measurement can serve as a diagnostic probe of engineered spin-orbit coupling.
Spin-orbit coupling in semiconductors wolf01 () and at the surface of three dimensional topological insulators Hasan (); Moore1 (); Qi (); Bernevig (); Fu (); Chen1 (); Li3 () where protected metallic surface states exist, plays a crucial role in their fundamental physical properties. Similarly pseudospin leads to novel properties in graphene Mac (); Novo2 (); Zhang () and other two dimensional membranes, such as single layer Mak1 (); Splendiani (); Lebegue (); Lee (); Li12 (); Li13 () and silicene Drum (); Aufray (); Stille (); Ezawa1 (); Ezawa2 (). In particular has been discussed within the context of valleytronics where the valley degree of freedom can be manipulated with the aim of encoding information in analogy to spintronics. Spin-orbit coupling has also been realized in zincblende semiconductor quantum wells awschalom09 (); Walser (); bernevig06 () and neutral atomic Bose-Einstein condensates lin11 () at very low temperature bloch08 ().
In some systems both Rashba rashba60 () and Dresselhaus dresselhaus () spin-orbit coupling are manipulated, the former arising from an inversion asymmetry of the grown layer while the latter comes from the bulk crystal. In general spin-orbit coupling will lead to rotation of the spin of charge carriers as they change their momentum, because SU(2) symmetry is broken. In momentum space this has been observed by angle-resolved photoemission spectroscopy (ARPES) as the phenomenon of spin momentum locking. In a special situation when the strength of Rashba and Dresselhaus spin-orbit coupling are tuned to be equal, SU(2) symmetry is recovered and a persistent spin helix state is found awschalom09 (); Walser (); bernevig06 (). This state is robust against any spin-independent scattering. However it will be potentially destroyed by the cubic Dresselhaus term which is usually tuned to be negligible.
To describe these effects we consider a model Hamiltonian describing a free electron gas with kinetic energy given simply by , which describes charge carriers with effective mass . We also include spin-orbit coupling terms, with linear Rashba () and Dresselhaus () couplings, along with a cubic Dresselhaus () term. The Hamiltonian is
Here and are the Pauli matrices for spin (or pseudospin in a neutral atomic Bose-Einstein condensate) and is the unit matrix. For units we use a typical wave vector with corresponding energy , where is a representative spin-orbit coupling which has quite different values for semiconductors (, estimated from Ref. bernevig06 ()) and cold atoms (, estimated from Ref. lin11 ()). The mass of a cold atom is at least 1000 times heavier than that of an electron and the wavelength of the laser used to trap the atoms is at least 1000 times (estimated from Ref. lin11 ()) larger than the lattice spacing in semiconductors.
In this report we study the dynamic longitudinal optical conductivity of such a spin-orbit coupled 2D electron gas. We find that the interband optical absorption will disappear when the Rashba coupling is tuned to be equal to the Dresselhaus coupling strength. We discuss the effect of nonlinear (cubic) Dresselhaus coupling on the shape of the interband conductivity and the effect of the asymmetry between the conduction and valence band which results from a mass term in the dispersion curves.
We compute the optical conductivity (see Methods section) as a function of frequency, for various electron fillings and spin-orbit coupling strengths. In all our figures we will use a dimensionless definition of spin-orbit coupling; for example, the choice of values designated in the lower right frame of Fig. 1, , and , really means , and .
In Fig. 1 we plot the spin direction in the conduction band as a function of momentum for several cases. The top left frame is for pure Rashba coupling, in which case spin is locked to be perpendicular to momentum Hasan () as has been verified in spin angle-resolved photoemission spectroscopy studies Lanzara1 (); Lanzara2 (); Xu (); Wang (). The top right frame gives results for pure linear Dresselhaus coupling (no cubic term ). The spin pattern is now quite different; the direction of the spin follows the mirror image of the momentum about the x-axis. The lower left frame for equal linear Rashba and Dresselhaus coupling is the most interesting to us here. All spins are locked in one direction, namely with those in the bottom (upper) triangle pointing parallel (anti-parallel) to the direction, respectively. This spin arrangement corresponds to the persistent spin helix state of Ref. awschalom09 (); Walser (); bernevig06 (). The condition and is a state of zero Berry phase Shen1 () and was also characterized by Li et al. Shen () as a state in which the spin transverse “force” due to spin-orbit coupling cancels exactly. Finally the right lower frame includes a contribution from the cubic Dresselhaus term of Eq. (1) and shows a more complex spin arrangement. Spin textures have been the subject of many recent studies Lanzara1 (); Lanzara2 (); Xu (); Wang (); Khom (). In Fig. 2 we present results for the dispersion curves in the conduction and valence band of Eq. (10) as a function of momentum . The two left panels are pure Rashba (top) and Rashba equals to Dresselhaus (bottom, see also Fig.1 of Ref.Mars () where only the contour plots of the valence band is shown). The two right panels include the Dresselhaus warping cubic term which profoundly affects the band structure.
The optical conductivity is obtained through transitions from one electronic state to another. In general these can be divided into two categories — transitions involving states within the same band, and interband transitions. Here we focus on interband transitions; the interband optical conductivity is given by
where is the Fermi-Dirac distribution function with the chemical potential. For and , we have a cancellation in the optical matrix element, ; remarkably the interband contribution vanishes. This result is central to our work and shows that in the persistent spin helix state the interband contribution to the dynamic longitudinal optical conductivity vanishes. This is the optical signature of the existence of the spin helix state which exhibits remarkable properties. With the optical matrix element is . Thus, pure Rashba or pure (linear) Dresselhaus coupling will both lead to exactly the same conductivity although the states (and spin texture) involved differ by a phase factor of . When they are both present in equal amounts this phase leads to a cancelation which reduces the interband transitions to zero as the two contributions need to be added before the square is taken. Of course the joint density of states, widely used to discuss optical absorption processes, remains finite. It is given by
and will be contrasted with the interband optical conductivity below.
We first focus on the case . The interband conductivity is shown in Fig. 3 as a function of frequency for positive (top frame) and negative (bottom frame) chemical potential (). It is clear that there is a considerable difference between the two cases, and there is also considerable variation with the degree of Rashba vs. Dresselhaus coupling. This will be discussed further below. Most important is that for equal amounts of Rashba and Dresselhaus coupling, the interband conductivity is identically zero for all frequencies.
What is the impact of a finite value of ? In Fig. 4 we show both the joint density of states (top two panels) and the interband conductivity (bottom two panels) for non-zero for (left panels) and (right panels). Various combinations of , and are shown as labeled on the figure. There is a striking asymmetry between positive and negative values of the chemical potential. This asymmetry has its origin in the quadratic term of the Hamiltonian (1) which adds positively to the energy in both valence and conduction band while the Dirac like contribution is negative () and positive () respectively [see Eq. (10)]. While the quadratic piece drops out of the energy denominator in Eq. (2) it remains in the Fermi factors and .
Several features of these curves are noteworthy. They all have van Hove singularities which can be traced to extrema in the energy difference . Taking for simplicity, this energy becomes which depends on the direction () of momentum , but has no minimum or maximum as a function of . To get an extremum one needs to have a non-zero cubic Dresselhaus term. This gives dispersion curves which flatten out with increasing values of . The dependence of the energy on momentum is illustrated in Fig. 5 where we provide a color plot for this energy as a function of and for two sets of spin-orbit parameters (top panel) and (bottom panel). Note the saddle points correspond to the most prominent van Hove singularities in the joint density of states (and conductivity) in Fig. 4. The van Hove singularities are at about ( in the momentum space) in the top frame of Fig. 5 and at about () and () in the bottom.
The optical conductivity is often characterized by the joint density of states, , which has a finite onset at small energies. This is well known in the graphene literature where interband transitions start exactly at a photon energy equal to twice the chemical potential. Here this still holds approximately in all the cases considered in Fig. 4 except for the solid red curve in the two left side frames. In this case and is non zero. If is small the energy would be approximately equal to , which is zero for , the critical angle in the spin texture of the lower left frame of Fig. 1 for which all spins are locked in this direction. This means that only the quadratic term and cubic Dresselhaus term contribute to the dispersion curve in this direction and there is no linear (in ) graphene-like contribution. Thus, the onset of the interband optical transition no longer corresponds to .
Considering the case of positive , for the direction , is the dominant contribution to the energy which is equal to and the minimum photon energy is now , which could be very small as is clear from the figure. For negative values of the onset is closer to because in this case the momentum at which the chemical potential crosses the band dispersion is given by (the cubic term is ignored because it is subdominant for small compared to the linear term). Now the photon energy onset will fall above , at a value dependent on .
While the optical conductivity Eq. (2) requires a non-zero joint density of states Eq. (3), the additional weighting of in can introduce considerable changes to its dependence May () as we see in Fig. 3 and Fig. 4. In the top frame of Fig. 3, and there are no van Hove singularities because the Dirac contribution to the dispersion curves simply increases with increasing . The solid black and dashed red curves both reduce to the pure graphene case with onset exactly at and flat background beyond. The dotted red curve for mixed linear Dresselhaus and Rashba is only slightly different. The onset is near but below and the background has increased in amplitude. It is also no longer completely flat to high frequency; instead it has a kink near after which it drops. The dash-dotted black curve for and has changed completely with background reduced to near zero but with a large peak corresponding to an onset which has shifted to a value much less than . Finally for the entire interband transition region is completely depleted as we know from Eq. (2).
In Fig. 4 there is (non-zero) cubic Dresselhaus coupling present. The solid red curves, for which but with illustrate that the conductivity on the left (positive ) is non-zero, and is necessary for a vanishing interband conductivity at all photon energies. We see, however, that these transitions have been greatly reduced below what they would be in graphene for all photon energies except for a narrow absorption peak at much less than . For negative values of , on the other hand, even with the conductivity is zero.
The experimental observation of such a narrow low energy peak together with high energy van Hove singularities could be taken as a measure of nonzero . It is interesting to compare these curves for the conductivity with the joint density of states (lower frames). The color and line types are the same for both panels. The onset energy as well as energies of the van Hove singularities are unchanged in going from the joint density of states to the conductivity. Also, as is particularly evident in the dotted black and short dashed red curves the factor in leads to a nearly flat background for the conductivity as compared with a region of nearly linear rise in the density of states. This is true for both positive and negative values of .
In conclusion we have calculated the interband longitudinal conductivity as a function of photon energy for the case of combined Rashba and Dresselhaus spin-orbit coupling. We have also considered the possibility of a cubic Dresselhaus contribution. We find that in the persistent spin helix state when the spins are locked at an angle of independent of momentum, which arises when the linear Rashba coupling is equal to the linear Dresselhaus coupling, the interband optical transitions vanish and there is no finite energy absorption from these processes. Only the Drude intraband transitions will remain. When the cubic Dresselhaus term is nonzero the cancelation is no longer exact but we expect interband absorption to remain strongly depressed for photon energies above as compared, for example, to the universal background value found in single layer graphene. We propose interband optics as a sensitive probe of the relative size of Rashba and Dresselhaus spin orbit coupling as well as cubic corrections.
The optical conductivity is given by
Here is the temperature and is a trace over the matrix, and and are the Fermion and Boson Matsubara frequencies respectively with and integers. To get the conductivity which is a real frequency quantity, we needed to make an analytic continuation from imaginary to , where is real and is an infinitesimal. The velocity operators and are given by
Here , , , , and .
The Green’s function can be written as grimaldi06 ()
The wave function is given by
with corresponding eigenvalues
Here creates a particle with momentum and spin up (down). The spin expectation values work out to be
These formulas allow us to calculate the spin texture, as well as the optical conductivity as given in Eq. (2).
Acknowledgements.This work was supported by the Natural Sciences and Engineering Research Council of Canada (NSERC), the Canadian Institute for Advanced Research (CIFAR), and Alberta Innovates.
V Author Contributions
ZL carried out the calculations, and all authors, ZL, FM, and JPC contributed equally to the development of the work.
Vi Competing financial interests
The authors declare no competing financial interests.
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