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Transport Properties of A Two-Dimensional Electron Gas Dressed by Light
Transport Properties of A Two-Dimensional Electron Gas Dressed by Light
Transport Properties of A Two-Dimensional Electron Gas Dressed by Light
We show theoretically that the strong interaction of a two-dimensional electron gas (2DEG)
with a dressing electromagnetic field drastically changes its transport properties. Particularly, the
dressing field leads to the giant increase of conductivity (which can reach thousands of percents),
results in nontrivial oscillating dependence of conductivity on the field intensity, and suppresses
the weak localization of 2DEG. As a consequence, the developed theory opens an unexplored way
to control transport properties of 2DEG by a strong high-frequency electromagnetic field. From
experimental viewpoint, this theory is applicable directly to quantum wells exposed to a laser-
generated electromagnetic wave.
field. It follows from the basic principles of quantum III. CONDUCTIVITY OF DRESSED 2DEG
optics that the strong coupling of electrons to such a
dressing field leads to the renormalization of all physical Assuming the temperature to be zero, let us apply a
quantities describing the electrons.4,5 Particularly, it is stationary (dc) electric field E to the 2DEG. It follows
well-known that a high-frequency electromagnetic field from the conventional Boltzmann equation for conduc-
can strongly affect the scattering of conduction electrons tion electrons (see, e.g., Ref. [32]) that electric current
and change electronic transport characteristics.34,35 Re- density, J, is given by the well-known expression
cently, this approach was extended for the case of a two- Z
dimensional electron gas subjected to a purely dressing e2
field which cannot be absorbed and emitted by conduc- J= [E · v(k)] τ (k)v(k)δ(εk − εF )d2 k, (6)
2π 2
tion electrons.29 Namely, the scattering probability of a k
dressed electron between electron states with wave vec-
where v(k) = (1/~)∇k εk is the electron velocity, εF =
tors k and k′ per unit time has the form29
~2 k2F /2m is the electron Fermi energy, and τ (k) is the
2π 2 relaxation time. In the most general case of anisotropic
2
wk′ k = J (fk′ k ) |Uk′ k | δ(εk′ − εk ), (3) electron scattering, this relaxation time is given by the
~ 0
equation33
where J0 (z) is the zeroth order Bessel function of the first 1 X τ (k′ )E · v(k′ )
kind, and Uk′ k is the matrix element of the scattering = 1− wk′ k . (7)
potential, U (r), which arises from macroscopically large τ (k) τ (k)E · v(k)
′ k
number of scatterers in the conductor. In the case of
linearly polarized dressing field,29 the argument of the Since absorption of a high-frequency field satisfying in-
Bessel function is given by equality (2) is negligibly small, the field does not change
the equilibrium distribution function of electrons.29
eEω (k − k′ ) Therefore, the field influences on the stationary (dc)
fk′ k = , (4) transport of dressed electrons only through the renor-
mω 2
malization of the scattering probability, wk′ k , given by
where Eω is the amplitude of the electric field of the Eq. (3). It should be stressed that the condition (2) is
e
wave, E(t) = Eω sin ωt. In the case of circularly polarized crucial in order to consider a 2DEG subjected to the field
dressing field (see Appendix A), this argument is as an equilibrium system. Otherwise, the photon-assisted
scattering of electrons is accompanied by absorption of
field energy and leads to heating 2DEG. In this case,
2Eω ek θk ′ k
f k′ k = sin , (5) there are no stationary transport characteristics of the
mω 2 2
2DEG and the problem should be reformulated in terms
of the non-equilibrium electron transport.
where θk′ k = (kd ′ , k) is the angle between electron wave
Substituting the scattering probability of dressed elec-
′
vectors k and k . The formal difference between the scat- tron (3) into Eq. (7), we can obtain from Eqs. (6)–(7) the
tering probability of dressed electron (3) and the conven- conductivity of dressed 2DEG, σij = Ji /Ej .
tional expression for the scattering probability of bare To simplify calculations, let us consider the electron
electron31 consists in the Bessel-function factor J02 (fk′ k ), scattering within the s-wave approximation,31 where the
where fk′ k depends on the dressing field amplitude Eω matrix elements Uk′ k do not depend on the angle θk′ k =
and the dressing field frequency ω [see Eqs. (4)–(5)]. Just (kd′ , k). Substituting Eq. (5) into Eqs. (3) and (6)–(7),
this factor results in nontrivial dependence of electronic we arrive at the isotropic conductivity of 2DEG dressed
transport properties on the dressing field. In what fol- by circularly polarized field, σc , which is given by the
lows, we will focus our attention on the conductivity and expression
the weak localization of dressed 2DEG.
Z 2π −1
σc 2eEω kF θ
= 2π [1 − cos θ]J02 2
sin dθ ,
σ0 0 mω 2
(8)
where σ0 is the conductivity of an unirradiated 2DEG.
In the case of linearly polarized dressing field, the con-
ductivity tensor σij has a simple diagonal form, σii =
(σk , σ⊥ ), in the basis of two axes which are parallel (k)
and perpendicular (⊥) to the wave field E, e respectively.
FIG. 1: (Color online) Sketch of the system under consid-
eration: The 2DEG dressed by (a) linearly polarized high- Substituting Eq. (4) into Eqs. (3) and (6)–(7), we arrive
e and (b) circularly polarized one in the pres-
frequency field E at
ence of a stationary in-plane electric field E = (Ek , E⊥ ). Z
σk 1 2π τk (θ)
= cos2 θdθ (9)
σ0 π 0 τ0
3
and
Z 2π
σ⊥ 1 τ⊥ (θ)
= sin2 θdθ (10)
σ0 π 0 τ0
where τk (θ) and τ⊥ (θ) are the relaxation time (7) at the
Fermi energy for the dc electric field E = (Ek , 0) and
d
E = (0, E⊥ ), respectively (see Fig. 1a), and θ = (k, E).
The difference between the conductivities σk and σ⊥ where C(t) is the probability to find an electron in the
arises from the scattering anisotropy of a 2DEG dressed initial point of its trajectory at the time t averaged over
by a linearly polarized field, which follows directly from 2DEG plane, τF is the mean free time of conduction elec-
Eqs. (3)-(4). It should be stressed that the arguments tron at the Fermi energy, which is given by the expression
of the Bessel function in the scattering probability (3) X
1
for the cases of linearly polarized field (4) and circularly = wkF k′F , (12)
polarized field (5) strongly differ from each other. There- τF ′ kF
fore, the integration over k and k′ and in the scattering
probability (3) substituted into the kinetic Boltzmann and τϕ is the effective breaking-time of electron phase.
equation leads to strongly different plots in Fig. 2 for lin- Generally, electron phase can be broken by both in-
ear polarization and circular polarization. Particularly, elastic scattering and a magnetic field which destroy
the amplitude of oscillations of conductivity in the case WL.39–44 The breaking-time of electron phase caused
of linear polarization is nonzero but very small as com- by a magnetic field, B, is τϕB = ~/4eDB, where D is
pared to the case of circular polarization. Therefore, the the diffusion constant.44 Correspondingly, the effective
most appropriate experimental set for observing the os- breaking-time of electron phase, τϕ , can be written as
cillations should be based on using circularly polarized 1/τϕ = 1/τϕε + 1/τϕB , where τϕε is the characteristic
light. breaking-time arisen from inelastic processes. As to the
4
mean free time of conduction electron, τF , it can be found due to intraband absorption of irradiation by conduction
by substituting the scattering probability of dressed elec- electrons.47–49 Indeed, under the condition (2) there is
tron (3) into Eq. (12). It has been mentioned above no absorption of high-frequency field by conduction elec-
that this scattering probability is anisotropic for 2DEG trons. Therefore, the destruction of WL, which arises
dressed by a linearly polarized field. Therefore, the time from the breaking of electron phase in inelastic electron-
(12) depends on the initial electron wave vector kF . To photon processes,47–49 is negligibly small in the 2DEG
describe this anisotropy, it is suitable to introduce the under consideration. As a consequence of decreasing WL
two mean free times: τF k and τF ⊥ for the cases of kF k Ee effects, the influence of a magnetic field on WL correc-
e
and kF ⊥ E, respectively. Substituting these two times tions to the conductivity for a dressed 2DEG is less than
into Eq. (11), we arrive at the two WL corrections, ∆σk one for a bare 2DEG (see the insert in Fig. 3). It should
and ∆σ⊥ . These two corrections describe the conduc- be noted that the WL correction to the conductivity
tivity of dressed 2DEG for the cases of E = (Ek , 0) and of 2DEG has a logarithmic dependence on a magnetic
E = (0, E⊥ ), respectively (see Fig. 1a). Certainly, in the field.36 Although the irradiation on the 2DEG reduces
case of circularly polarized dressing field, the anisotropy WL corrections, the behavior of conductivity of dressed
vanishes and the corresponding WL correction, ∆σc , does 2DEG in a magnetic field obeys the same law. As to
not depend on direction in the 2DEG plane. small oscillations visible in Fig. 3, they have the same
Within the conventional theory of WL, the probability nature as oscillations of conductivity pictured in Fig. 2.
C(t) in Eq. (11) can be described by the Feynman path Anisotropy of weak localization in the case of linearly po-
integral37,45 larized field is within one percent and cannot be easily
detected experimentally. Therefore, we have ∆σk ≈ ∆σ⊥
Z " Z
t/2
ẋ2 ẏ 2 for the plots in Fig. 3.
C(t) = DxDy exp − +
−t/2 4Dx 4Dy
#
i e ′ ) − E(−t
e ′
− er[E(t )]dt′ , (13)
~
The work was partially supported by FP7 IRSES Let an electron move in a scattering potential U (r) in
projects POLATER and QOCaN, FP7 ITN project the presence of the same field. Then the wave function of
NOTEDEV, Tier 1 project “Polaritons for novel de- the electron, Ψ(r, t), satisfies the Schrödinger equation
vice applications”, Rannis project BOFEHYSS, RFBR
project 14-02-00033, and the Russian Ministry of Educa- ∂Ψ(r, t)
i~ = [Ĥ0 + U (r)]Ψ(r, t). (A4)
tion and Science. ∂t
Assuming the scattering potential energy U (r) to be
a small perturbation, we can apply the conventional
Appendix A: Scattering of 2DEG dressed by a perturbation theory to describe the electron scattering.
circularly polarized electromagnetic field Since the functions (A3) with different wave vectors k
form the complete function system for any time t, we
For definiteness, we will restrict our consideration to can seek solutions of the Schrödinger equation (A4) as
the case of a two-dimensional electron system subjected an expansion
to a circularly polarized electromagnetic wave propagat- X
ing perpendicularly to the system. Let the system lie in Ψ(r, t) = ak′ (t)ψk′ (r, t). (A5)
the plane (x, y) at z = 0 and the wave propagate along k′
the z axis. Then the electron properties of the system in
the absence of scatterers are described by the Schrödinger Let an electron be in the state (A3) with the wave vector
equation k at the time t = 0. Correspondingly, ak′ (0) = δk′ ,k ,
where δk′ ,k is the Kronecker symbol. In what follows, we
∂ψ will assume that the wave frequency ω is large enough to
i~ = Ĥ0 ψ (A1) satisfy the inequality
∂t
with the Hamiltonian Ĥ0 = [p̂ − eA(t)]2 /2m, where p̂ = ωτ0 ≫ 1, (A6)
(p̂x , p̂y ) is the operator of electron momentum, m is the
effective electron mass, e is the electron charge, where τ0 is the characteristic relaxation time of conduc-
tion electron in the absence of the wave. Under the
A(t) = ex (Eω /ω) sin ωt + ey (Eω /ω) cos ωt condition (A6), we can neglect the absorption (emis-
sion) of field energy by a scattered electron (see, e.g.,
Refs. [27,28]). Within this approximation, the scatter-
is the vector potential of the wave, Eω is the electric field
ing potential U (r) mixes only electron states k and k′
amplitude of the wave, ω is the frequency of the wave,
with the same energy, εk = εk′ .29 Therefore, it is enough
and ex,y are the unit vectors along the x, y axis. The
to take into account only terms with k ′ = k in the ex-
Schrödinger equation (A1) can be solved accurately and
pansion (A5). Substituting the expansion (A5) into the
the exact wave function of the electron is
Schrödinger equation (A4) and restricting the accuracy
by the first order of perturbation theory, we arrive at the
εk t E 2 e2 t Eω eky
ψk (r, t) = exp −i + ω 2 − sin ωt expression
~ 2mω ~ mω 2
Eω ekx Zt
+ cos ωt ϕk (r), (A2) Uk′ k ′ ′ ′
mω 2 ak′ (t) = −i ei(εk′ −εk )t /~ eifk′ k sin[ωt +(ϕ+ϕ )/2] dt′ ,
~
0
where ϕk (r) = V −1/2 exp(ikr) is the plane electron wave, (A7)
k = (kx , ky ) is the electron wave vector, r = (x, y) is where
the electron radius-vector, V is the normalization vol-
ume, and εk = ~2 k 2 /2m is the energy spectrum of a free Uk′ k = hϕk′ (r) |U (r)| ϕk (r)i (A8)
electron. Evidently, the wave function (A2) can be eas-
ily verified by direct substitution into the Schrödinger is the matrix element of the scattering potential,
equation (A1). Introducing the polar system {k, ϕ}, we
can write the electron wave vectors as kx = k cos ϕ and 2Eω ek θ
fk k =
′ sin , (A9)
ky = k sin ϕ. Then the wave function (A2) takes the mω 2 2
6
d
and θ = ϕ − ϕ′ = (k, k′ ) is the scattering angle. Let us To transform the square delta-functions in Eq. (A11), we
apply the Jacobi-Anger expansion, can apply the conventional procedure,
∞
X
eiz sin γ = Jn (z)einγ ,
n=−∞
Zt/2
in order to rewrite Eq. (A7) as 2 δ(ε) ′ δ(ε)t
δ (ε) = δ(ε)δ(0) = lim ei0×t /~ dt′ = .
∞ 2π~ t→∞ 2π~
|Uk′ k | X
2 −t/2
2
|ak′ (t)| = Jn (fk′ k ) ei(εk′ −εk +n~ω)t/2~
~2 n=−∞
Zt/2 2
in(ϕ+ϕ′ )/2 i(εk′ −εk +n~ω)t′ /~ ′ Keeping in mind that εk = εk′ , the probability of the
× e e dt ,
electron scattering between the states (A2) with the wave
−t/2 vectors k and k′ per unit time, wk′ k = d|ak′ (t)|2 /dt, is
(A10) given by
∗
Electronic address: Oleg.Kibis(c)nstu.ru gione, O. Di Stefano, S. Patane, S. Savasta, D. Sanvitto
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