time-dependent density functional theoryd 1Δ 0.3759 0.3812 a' 3 Σ+ 0.3127 0.3181 e 3Σ-0.3631...
TRANSCRIPT
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Time-dependent density functional theory
Max-Planck Institute ofMicrostructure Physics
Halle (Saale)
E.K.U. Gross
OUTLINE
• Basics of TDDFT
• Linear response regime: -- Calculation of excitation spectra
• Beyond the linear regime: -- TD Electron Localisation Function -- TD transport-- Demagnetization of ferromagnetic solids-- Control of harmonic generation
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What do we want to describe?
System in laser field:Generic situation
α
++=, j
eee W T H(t) + rj·E(t)·sin ωt→→Zα e2
|rj-Rα|
What do we want to describe?
System in laser field:Generic situation
α
++=, j
eee W T H(t) + rj·E(t)·sin ωt→→Zα e2
|rj-Rα|
left lead Lcentral
region Cright lead R
Bias between L and R is turned on: U(t) V
Electronic transport: Generic situation
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α
++=, j
eee W T H(t) + rj·E(t)·sin ωt→→Zα e2
|rj-Rα|
Weak laser (vlaser(t) << ven) :
Calculate 1. Linear density response ρ1(r t)
2. Dynamical polarizability
3. Photo-absorption cross section
→
( ) ( ) ωρ−=ωα rd,r zE
e 31
( ) απω−=ωσ Imc
4
Strong laser (vlaser(t) ≥ ven) :
Non-perturbative solution of full TDSE required
Photo-absorption in weak lasers
continuum states
unoccupied bound states
occupied bound states
I1
I2
Laser frequency ω
σ(ω)
ph
oto-
abso
rpti
on c
ross
sec
tion
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Example: Oxygen atom (8 electrons)
depends on 24 coordinates
rough table of the wavefunction
10 entries per coordinate: 1024 entries
1 byte per entry: 1024 bytes
1010 bytes per DVD: 1014 DVDs
10 g per DVD: 1015 g DVDs
= 109 t DVDs
( )81 r,,rΨ
Why don’t we just solve the many-particle SE?
ESSENCE OF DENSITY-FUNTIONAL THEORY
• Every observable quantity of aquantum system can be calculatedfrom the density of the systemALONE
• The density of particles interactingwith each other can be calculated asthe density of an auxiliary system ofnon-interacting particles
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Basic 1-1 correspondence:The time-dependent density determines uniquelythe time-dependent external potential and hence allphysical observables for fixed initial state.
( ) ( )v rt rt1-1←⎯→ ρ
Time-dependent density-functional formalism
KS theorem:
The time-dependent density of the interacting system of interest canbe calculated as density
of an auxiliary non-interacting (KS) system
with the local potential
( ) ( )2N
j = 1
ρ r t = r tjϕ
( ) ( ) ( ) ( )3S
r ' tv r ' t ' rt v rt d r '
r r '
ρ ρ = + + −
( ) [ ]( ) ( )2 2
j S ji rt v rt rtt 2m
∂ ∇ϕ = − + ρ ϕ ∂
( ) ( )xcv r ' t ' rt ρ
(E. Runge, E.K.U.G., PRL 52, 997 (1984))
The functional vxc[ρ] is universal:
Curse or blessing?
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The functional vxc[ρ] is universal:
Curse or blessing?
Only ONE functional needs to be approximated
The functional vxc[ρ] is universal:
Curse or blessing?
Only ONE functional needs to be approximated
Functional can be systematically improved, i.e. results will improve -on average- for all systems. Systematic improvementfor a single given system is not possible.
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proof (basic idea):
i.e. v(r t) ≠ v’(r t) + c(t) ρ(r t) ≠ ρ’(r t)→
to be shown that is impossible)t r(v
)t r('v
→
)t r(' )t r('j )t r(v
)t r( )t r(j )t r(v
ρ
ρ
'
→ →
ρ(r t)
( )
φφ=∂ t tH , rj ttrj t
i
equation of motion for j→
and ( )( ) j
rtdiv rt
t
∂ρ∂
= −
continuity equation
to show that and
0
0 tt tt
t
'j
t
j
==∂∂≠
∂∂
0
0 t
2
2
t
2
2
t
'
t ∂ρ∂≠
∂ρ∂
use
ρ and ρ’ will become differentfrom each other infinitesimallylater than t0
ρ’(t)
ρ(t)
t0 t
ρ(t)
( )
φφ=∂ t tH , rj ttrj t
i
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Simplest possible approximation for [ ]( )trρvxc
Adiabatic Local Density Approximation (ALDA)
( ) ( ) nv : t rv)t r(n
homstat,xc
ALDAxc
ρ=
=
homstat,xcv = xc potential of static homogeneous e-gas
Approximation with correct asymptotic -1/r behavior:time-dependent optimized effective potential (TDOEP)
C. A. Ullrich, U. Gossmann, E.K.U.G., PRL 74, 872 (1995)
LINEAR RESPONSE THEORY
t = t0 : Interacting system in ground state of potential v0(r) with density ρ0(r)
t > t0 : Switch on perturbation v1(r t) (with v1(r t0)=0).
Density: ρ(r t) = ρ0(r) + δρ(r t)
Consider functional ρ[v](r t) defined by solution of interacting TDSE
Functional Taylor expansion of ρ[v] around vo:
[ ]( ) [ ]( )tr vρtrvρ 0 += 1v
[ ]( )( )+ dt'r'd
t'r' δv
tr vδρ 3
0v
( )'t'rv1
[ ]( )tr vρ 0 =
[ ]( )( ) ( ) + dt"dt'r"dr'd
t"r" δvt'r' δv
tr vρδ
2
1 332
0v
( ) ( )"t,"rv't,'rv 11 ( )r tρ2
( )r tρ1
( )rρo
…
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ρ1(r,t) = linear density response of interacting system
( ) [ ]( )( )
0v
t'r' δv
tr vδρ:'t'r,tr =χ = density-density response function of
interacting system
Analogous function ρs[vs](r t) for non-interacting system
[ ]( ) [ ]( ) [ ]( ) [ ]( )( ) ++=+= dt'r'd
t'r'δv
r t vδρr t vρr t vρr t vρ 3
S
SSS,0SS,0SSS
S,0v
S,1v ( )t'r'vS,1
( ) [ ]( )( )
S,0v
t'r'δv
tr vδρ:'t'r,tr
S
SSS =χ = density-density response function of
non-interacting system
GOAL: Find a way to calculate ρ1(r t) without explicitly evaluating
χ(r t,r't') of the interacting system
starting point: Definition of xc potential
[ ]( ) [ ]( ) [ ]( ) [ ]( )r tρvr tρvr tρv:r tρv HextSxc −−=
vxc is well-defined through non-interacting/ interacting 1-1 mapping.
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[ ]( )( )
[ ]( )( )
[ ]( )( )
( )r'r
t'tδ
t'r'δρ
r tρδv
t'r'δρ
r tρδv
t'r'δρ
r tρδv extSxc
−−−−=
000 ρρρ
[ ]( )( )
[ ]( )( )
[ ]( )( )
( )r'r
t'tδ
t'r'δρ
r tρδv
t'r'δρ
r tρδv
t'r'δρ
r tρδv extSxc
−−−−=
000 ρρρ
( )t'r'r t,fxc ( )t'r'r t,1S−χ ( )t'r'r t,1−χ ( )t'r'r t,WC
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[ ]( )( )
[ ]( )( )
[ ]( )( )
( )r'r
t'tδ
t'r'δρ
r tρδv
t'r'δρ
r tρδv
t'r'δρ
r tρδv extSxc
−−−−=
000 ρρρ
( )t'r'r t,fxc ( )t'r'r t,1S−χ ( )t'r'r t,1−χ ( )t'r'r t,WC
11SCxc Wf −− χ−χ=+
[ ]( )( )
[ ]( )( )
[ ]( )( )
( )r'r
t'tδ
t'r'δρ
r tρδv
t'r'δρ
r tρδv
t'r'δρ
r tρδv extSxc
−−−−=
000 ρρρ
( )t'r'r t,fxc ( )t'r'r t,1S−χ ( )t'r'r t,1−χ ( )t'r'r t,WC
11SCxc Wf −− χ−χ=+ • χχS •
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[ ]( )( )
[ ]( )( )
[ ]( )( )
( )r'r
t'tδ
t'r'δρ
r tρδv
t'r'δρ
r tρδv
t'r'δρ
r tρδv extSxc
−−−−=
000 ρρρ
( )t'r'r t,fxc ( )t'r'r t,1S−χ ( )t'r'r t,1−χ ( )t'r'r t,WC
11SCxc Wf −− χ−χ=+ • χχS •
( ) SCxcS χχχ Wfχ −=+
( )S S ee xcχ χ χ W f χ= + +
Act with this operator equation on arbitrary v1(r t) and use χ v1 = ρ1 :
• Exact integral equation for ρ1(r t), to be solved iteratively
• Need approximation for
(either for fxc directly or for vxc)
( ) ( ) ( ) ( ) ( ) ( )ee
= + + 3 3
1 S 1 xc 1ρ r t d r'dt'χ r t,r't' v r t d r"dt" W r't',r"t" f r't',r"t" ρ r"t"
( ) [ ]( )( )
0ρt"r"δρ
t'r'ρδvt"r",t'r'f xc
xc =
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Total photoabsorption cross section of the Xe atom versus photonenergy in the vicinity of the 4d threshold.
Solid line: self-consistent time-dependent KS calculation [A. Zangwill and P.Soven, Phys. Rev. A 21, 1561 (1980)]; crosses: experimental data [R. Haensel, G.Keitel, P. Schreiber, and C. Kunz, Phys. Rev. 188, 1375 (1969)].
Photo-absorption in weak lasers
continuum states
unoccupied bound states
occupied bound states
I1
I2
Laser frequency ω
σ(ω)
ph
oto-
abso
rpti
on c
ross
sec
tion
Previous slide
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Looking at those frequencies, Ω, for which ρ1(ω) has poles,leads to the (non-linear) eigenvalue equation
(T. Grabo, M. Petersilka, EKUG, J. Mol. Struc. (Theochem) 501, 353 (2000))
( )( ) q'q
'q'qqq'qq A βΩ=βδω+Ωwhere
( ) ( ) ( )r'ΦΩ,r'r,fr'r
1 rΦ'rdrdαA q'xcq
33q'qq'
+
−=
( )a,jq =
( ) ( ) ( )rrr j*aq ϕϕ=Φ
jaq ff −=α
jaq ε−ε=ω
double index
Atom Experimental Excitation
Energies 1S→1P (in Ry)
KS energy differences Δ∈KS (Ry)
Δ∈KS + K
Be 0.388 0.259 0.391
Mg 0.319 0.234 0.327
Ca 0.216 0.157 0.234
Zn 0.426 0.315 0.423
Sr 0.198 0.141 0.210
Cd 0.398 0.269 0.391
from: M. Petersilka, U. J. Gossmann, E.K.U.G., PRL 76, 1212 (1996)
TDDFT
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Excitation energies of CO molecule
State Ωexpt KS-transition Δ∈KS Δ∈KS + K
A 1Π 0.3127 5Σ→2Π 0.2523 0.3267
a 3Π 0.2323 0.2238
I1Σ - 0.3631 1Π→2Π 0.3626 0.3626
D 1Δ 0.3759 0.3812
a'3Σ+ 0.3127 0.3181
e3Σ - 0.3631 0.3626
d3Δ 0.3440 0.3404
approximations made: vxc and fxcLDA ALDA
T. Grabo, M. Petersilka and E.K.U. Gross, J. Mol. Struct. (Theochem) 501, 353 (2000)
TDDFT
Failures of ALDA in the linear response regime
• response of long chains strongly overestimated(see: Champagne et al., J. Chem. Phys. 109, 10489 (1998) and 110, 11664 (1999))
• in periodic solids, whereas,
for insulators, divergent.2
0qexactxc q1 f ⎯⎯→⎯ →
( ) ( )ρ=ρω c,,qf ALDAxc
• charge-transfer excitations not properly described (see: Dreuw et al., J. Chem. Phys. 119, 2943 (2003))
• H2 dissociation is incorrect:
(see: Gritsenko, van Gisbergen, Görling, Baerends, J. Chem. Phys. 113, 8478 (2000))
( ) ( ) 0 EERg
1u
1 ⎯⎯ →⎯Σ−Σ ∞→++ (in ALDA)
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Failures of ALDA in the linear response regime
• response of long chains strongly overestimated(see: Champagne et al., J. Chem. Phys. 109, 10489 (1998) and 110, 11664 (1999))
• in periodic solids, whereas,
for insulators, divergent.2
0qexactxc q1 f ⎯⎯→⎯ →
( ) ( )ρ=ρω c,,qf ALDAxc
• charge-transfer excitations not properly described (see: Dreuw et al., J. Chem. Phys. 119, 2943 (2003))
• H2 dissociation is incorrect:
(see: Gritsenko, van Gisbergen, Görling, Baerends, J. Chem. Phys. 113, 8478 (2000))
( ) ( ) 0 EERg
1u
1 ⎯⎯ →⎯Σ−Σ ∞→++ (in ALDA)
These difficulties have largely been solved by xc functionals more advanced than ALDA
Source: Web of Science as of June 2015
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How can one give a rigorous mathematical meaning to chemical concepts such as
• Single, double, triple bonds• Lone pairs
Note: • Density ρσ (r) is not useful!• Orbitals are ambiguous (w.r.t. unitary
transformations)
Time-Dependent Electron Localization Function
( ) ( )( )
D r, r'P r, r' :
rσσ
σσ
=ρ
= conditional probability of finding an electronwith spin σ at if we know with certainty thatthere is an electron with the same spin at .
= diagonal of two-body density matrix
( ) ( )3 4 N
23 33 N 3 3 N N
...
D r, r' d r ... d r r , r' , r ..., rσσ σ σ
= Ψ σ σ σ σ
= probability of finding an electron with spin σ at and another electron with the same spin at .
r
r'
r'
r
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Coordinate transformation
r'
r
s If we know there is an electron with spin σ at , thenis the (conditional) probability of
finding another electron at .
( ) ( ) ( ) ( ) 2
s 0
dp r, s 1p r, s p r, 0 s C r s
ds 3σ
σ σ σ
=
= + ⋅ +
0 0
Expand in a Taylor series:
The first two terms vanish.
Spherical average ( ) ( )2
0 0
1p r, s sin d d P r, s , ,
4
π π
σ σ= θ θ ϕ θ ϕπ
r
( )P ,σ +r r s
r + s
If we know there is an electron with spin σ at , then is theconditional probability of finding another electron at the distance sfrom .
( )p ,r sσr
is a measure of electron localization.
small means strong localization at
( )σC r
Why? , being the s2-coefficient, gives the probability of
finding a second like-spin electron very near the reference
electron. If this probability very near the reference electron is
low then this reference electron must be very localized.
( )σC r
( )σC r
r
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Cσ is always ≥ 0 (because pσ is a probability) and is notbounded from above.
Define as a useful visualization of localization(A.D. Becke, K.E. Edgecombe, JCP 92, 5397 (1990))
1 ELF 0 ≤≤Advantage: ELF is dimensionless and
where
is the kinetic energy density of the uniform gas.
( )( )
1
1ELF 2
rC
rCuni
σ
σ+=
( ) ( ) ( ) ( )rr65
3rC uni35322uni
σσσ τ=ρπ=
( )σC r
ELF
A. Savin, R. Nesper, S. Wengert, and T. F. Fässler, Angew. Chem. Int. Ed. 36, 1808 (1997)
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For a determinantal wave function one obtains
( ) ( ) ( )( )( )
2N
2deti
i 1
r1C r r
4 r
σσ
σ σ= σ
∇ρ= ∇ϕ −
ρ
in the static case:
(A.D. Becke, K.E. Edgecombe, JCP 92, 5397 (1990))
in the time-dependent case:
(T. Burnus, M. Marques, E.K.U.G., PRA (Rapid Comm) 71, 010501 (2005))
( ) ( ) ( )( )( )
2N
2deti
i 1
r, t1C r, t r, t
4 r, t
σσ
σ σ= σ
∇ρ= ∇ϕ −
ρ
( ) ( )2
j r, t r, tσ σ− ρ
Acetylene in laser field(ħω = 17.15 eV, I = 1.2×1014 W/cm2)
Scattering of a proton from ethylene(Ekin(proton) = 2 keV)
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TDELF for acetylene in strong laser field(ħω = 17.15 eV, I = 1.2×1014 W/cm2)
TDELF for scattering process2 keV proton colliding with ethylene
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TDELF movies produced from TD Kohn-Sham equations
( )[ ]( ) ( ) ( ) +−ρ+=ρ 'rr
t'r'rdrtvrt't'rv 3
KSvxc[ρ (r’t’)](r t)
( ) [ ]( ) ( )rt rtvm2
rtt
i jKS
22
j ϕ
ρ+∇−=ϕ
∂∂
propagated numerically on real-space grid using octopus code
octopus: a tool for the application of time-dependent density functional theory, A. Castro, M.A.L. Marques, H. Appel, M. Oliveira, C.A. Rozzi, X. Andrade, F. Lorenzen, E.K.U.G., A. Rubio, Physica Status Solidi 243, 2465 (2006).
T. Burnus, M. Marques, E.K.U.G, PRA (Rapid Comm) 71, 010501 (2005)
Electronic transport with TDDFT
left lead Lcentral
region Cright lead R
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Electronic transport with TDDFT
left lead Lcentral
region Cright lead R
TDKS equation (E. Runge, EKUG, PRL 52, 997 (1984))
( )[ ]( ) ( ) ( ) +−ρ+=ρ 'rr
t'r'rdrtvrt't'rv 3
KSvxc[ρ (r’t’)](r t)
( ) [ ]( ) ( )rt rtvm2
rtt
i jKS
22
j ϕ
ρ+∇−=ϕ
∂∂
( )( )( )
( ) ( ) ( )( ) ( ) ( )( ) ( ) ( )
( )( )( )
ϕϕϕ
=
ϕϕϕ
∂∂
t
t
t
tHtHtH
tHtHtH
tHtHtH
t
t
t
ti
R
C
L
RRRCRL
CRCCCL
LRLCLL
R
C
L
left lead Lcentral
region Cright lead R
TDKS equation
Electronic transport with TDDFT
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Effective TDKS Equation for the central (molecular) region only
S. Kurth, G. Stefanucci, C.O. Almbladh, A. Rubio, E.K.U.G.,Phys. Rev. B 72, 035308 (2005)
( ) ( ) ( )ttHtt
i CCCC ϕ=ϕ∂∂
source term: L → C and R → C charge injection
memory term: C → L → C and C → R → C hopping
( ) ( ) ( ) ( )00,tGiH00,tGiH RRCRLLCL ϕ+ϕ+
( ) ( )[ ] ( ) ϕ++t
0
CRCRCRLCLCL 'tH't,tGHH't,tGH'dt
Note: So far, no approximation has been made.
UV(x)
left lead right leadcentral region
Numerical examples for non-interacting electrons
Recovering the Landauer steady state
Time evolution of current in response to bias switched on at time t = 0,
Fermi energy εF = 0.3 a.u.
Steady state coincides with Landauer formula
and is reached after a few femtoseconds
U
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Does one always reach a steady state after switching-on the bias?
Two-site Anderson model
E. Khosravi, A.M. Uimonen, A. Stan, G. Stefanucci, S. Kurth, R. van Leeuwen, E.K.U. Gross, Phys. Rev. B 85, 075103 (2012)
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ELECTRON PUMP
Device which generates a net current between twoelectrodes (with no static bias) by applying a time-dependent potential in the device region
Experimental realization : Pumping through carbonnanotube by surface acoustic waves on piezoelectricsurface (Leek et al, PRL 95, 256802 (2005))
-8 -4 0 4 8x/a.u.
-0.05
-0.025
0
0.025
0.05
n(x,
t)/a
.u.
-0.5
-0.25
0
0.25
0.5
U(x
,t)/a
.u.
Pumping through a square barrier (of height 0.5 a.u.) using a travelling wave in device regionU(x,t) = Uosin(kx-wt)(k = 1.6 a.u., w = 0.2 a.u.Fermi energy = 0.3 a.u.)
Patent: Archimedes (250 b.c.)
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Experimental result:
Current flows in direction opposite to sound wave
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Current goes in direction opposite to the external field !!
G. Stefanucci, S. Kurth, A. Rubio, E.K.U. Gross, Phys. Rev. B 77, 075339 (2008)
Laser-induced ultrafast demagnetization of solids:The first 100 femto-seconds
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Beaurepaire et al, PRL 76, 4250 (1996)
First experiment on ultrafast laser induced demagnetisation
Beaurepaire et al, PRL 76, 4250 (1996)
First experiment on ultrafast laser induced demagnetisation
More recent experiments show demagnetization in less than 100 fs
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Possible mechanisms for demagnetisation
Possible mechanisms for demagnetisation
• Direct interaction of spins with the magnetic component of the laserZhang, Huebner, PRL 85, 3025 (2000)
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Possible mechanisms for demagnetisation
• Direct interaction of spins with the magnetic component of the laserZhang, Huebner, PRL 85, 3025 (2000)
• Spin-flip electron-phonon scattering(ultimately leading to transfer of spin angular momentum to the lattice)Koopmans et al, PRL 95, 267207 (2005)
Possible mechanisms for demagnetisation
• Direct interaction of spins with the magnetic component of the laserZhang, Huebner, PRL 85, 3025 (2000)
• Spin-flip electron-phonon scattering(ultimately leading to transfer of spin angular momentum to the lattice)Koopmans et al, PRL 95, 267207 (2005)
• Super-diffusive spin transportBattiato, Carva, Oppeneer, PRL 105, 027203 (2010)
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Possible mechanisms for demagnetisation
• Direct interaction of spins with the magnetic component of the laserZhang, Huebner, PRL 85, 3025 (2000)
• Spin-flip electron-phonon scattering(ultimately leading to transfer of spin angular momentum to the lattice)Koopmans et al, PRL 95, 267207 (2005)
• Super-diffusive spin transportBattiato, Carva, Oppeneer, PRL 105, 027203 (2010)
• Ab-initio (TDDFT) result for the first 50 fs: Laser-driven charge excitation followed by spin-orbit-driven demagnetization of the localized d-electrons
K. Krieger, J.K. Dewhurst, P.Elliott, S. Sharma, E.K.U. Gross, arXiv:1406.6607 (2014), to appear in JCTC (2015).
( ) ( )( ) [ ]( ) [ ]( )
[ ]( )( ) ( ) ( )
21, , , , ,
2
, , ,2
k laser S B S
BS k
i r t i A t v r t B r tt
v r t i r tc
ϕ ρ μ σ ρ
μ σ ρ ϕ
∂ = − ∇− + − ⋅∂ + ⋅ ∇ × − ∇
m m
m
Theoretical approach: TDDFT with SOC
[ ]( ) ( ) ( ) [ ]( )3,, , , ,S lattice xc
r tv r t v r d r v r t
r r
ρρ ρ
′′= + +
′−m m
[ ]( ) ( ) [ ]( ), , , , ,S external xcB r t B r t B r tρ ρ= +m m
( ),k r tϕwhere are Pauli spinors
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• Wave length of laser in the visible regime(very large compared to unit cell)
• Dipole approximation is made(i.e. electric field of laser is assumed to be spatially constant)
• Laser can be described by a purely time-dependent vector potential
• Periodicity of the TDKS Hamiltonian is preserved!
• Implementation in ELK code (FLAPW)(http://elk.sourceforge.net)
Aspects of the implementation
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Cr monolayer
Analysis of the results
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components of spin moment
Calculation without spin-orbit coupling
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Demagnetization occurs in two steps:
- Initial excitation by laser moves magnetization from MT regioninto interstitial region. Total Moment is basically conservedduring this phase.
- Spin-Orbit term drives demagnetization of localized electrons until stabilization at much lower moment is achieved
K. Krieger, J.K. Dewhurst, P. Elliott, S. Sharma, E.K.U. Gross, arXiv:1406.6607 (2014)
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Playing with laser parameters
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Influence of approximation for xc functional
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Problem: In all standard approximations of Exc (LSDA, GGAs)m(r) and Bxc(r) are locally collinear
S. Sharma, J.K. Dewhurst, C. Ambrosch-Draxl, S. Kurth, N. Helbig, S. Pittalis, S. Shallcross, L. Nordstroem E.K.U.G., Phys. Rev. Lett. 98, 196405 (2007)
Why is that important?
Ab-initio description of spin dynamics:
microscopic equation of motion (following from TDSDFT)
XC Sm(r, t) m(r, t) B (r, t) J (r, t)= × − ∇⋅
in absence of external magnetic field
Consequence of local collinearity: m×Bxc = 0: → wrong spin dynamics→ how important is this term in real-time dynamics?
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Construction of a novel GGA-type functional
Traditional LSDA: Start from uniform electron gas in collinear magnetic state. Determine from QMC or MBPT and parametrize touse in LSDA.
New non-collinear functional: Start from spin-spiralphase of e-gas. Determine from MBPT andparametrize to use as non-collinear GGA.
XCe [n, m]
XCe [n, m]
XCe [n, m]XCe [n, m]
F.G. Eich and E.K.U. Gross, Phys. Rev. Lett. 111, 156401 (2013)
( )( )( )
2
scos
m m ssin
1 s
⋅
= ⋅ −
q r
r q r
Magnetisation of a spin-spiral state in the uniform electron gas
SSW SSWxc xc (n, m,q,s)ε = ε
Illustration of spin spiral waves along one spatial coordinate for two different choices of wavevectorq=k1/2.
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( ) ( )( ) ( ) ( )
2T2
2 4T T
Ds
D m d=
+r
rr r r
( ) ( ) ( ) ( )( ) ( )
2 4T T2
4T
D m dq
m D
+=
r r rr
r r
[ ] ( ) ( ) ( ) ( ) ( )( )GGA 3 SSWxc xcE n, m d r n n , m ,q ,s= ε r r r r r
( ) ( ) ( )( ) 22
Td m m= × ∇r r r ( ) ( ) ( )( ) 2
TD m m= × ∇⊗r r r
F.G. Eich and E.K.U. Gross, Phys. Rev. Lett. 111, 156401 (2013)
m×Bxc
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Summary• No demagnetization without Spin-Orbit coupling
• Demagnetization in first 100 fs is a two-step process:1. Initial excitation of electrons into highly excited states
(without much of a change in the total magnetization)2. Spin-orbit coupling drives demagnetization of localized
electrons (mainly d electrons)
• Similar demagnetization behavior for Fe, Co, Ni
• No significant change in Mx and My
• New xc functional derived from spin-spiral phase of uniform e-gas
• Very little difference in demagnetization dynamics comparingthe new xc functional with the traditional non-collinear LSDA
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Optimal control of ultra-short processes
Review Article on Quantum Optimal Control Theory: J. Werschnik, E.K.U. Gross, J. Phys. B 40, R175-R211 (2007)
Normal question:
What happens if a system is exposed to a given laser pulse?
Inverse question (solved by OCT):
Which is the laser pulse that achieves a prescribed goal (target)?
Optimal Control Theory (OCT) of static targets
possible targets: a) system should end up in a given final state φf
at the end of the pulseb) wave function should follow a given trajectory in
Hilbert spacec) density should follow a given classical trajectory r(t)
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Optimal control of static targets(standard formulation)
( ) ( ) ( ) ( ) ( )TOTTTTJ f f 2
f 1 ΨΨ=ΨΦΦΨ=ΦΨ=
For given target state Φf , maximize the functional:
Optimal control of static targets(standard formulation)
( ) ( ) ( ) ( ) ( )TOTTTTJ f f 2
f 1 ΨΨ=ΨΦΦΨ=ΦΨ=
Ô
For given target state Φf , maximize the functional:
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Optimal control of static targets(standard formulation)
( ) ( ) ( ) ( ) ( )TOTTTTJ f f 2
f 1 ΨΨ=ΨΦΦΨ=ΦΨ=
Ô
( )
−εα−= 0
T
0
22 EtdtJ E0 = given fluence
with the constraints:
For given target state Φf , maximize the functional:
Optimal control of static targets(standard formulation)
( ) ( ) ( ) ( ) ( )TOTTTTJ f f 2
f 1 ΨΨ=ΨΦΦΨ=ΦΨ=
Ô
( )
−εα−= 0
T
0
22 EtdtJ E0 = given fluence
with the constraints:
[ ] ( ) ( )[ ] ( ) Ψμε−+−∂ι−χ−=χΨεT
0
t3 t tVT tdtIm2,,J
For given target state Φf , maximize the functional:
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Optimal control of static targets(standard formulation)
( ) ( ) ( ) ( ) ( )TOTTTTJ f f 2
f 1 ΨΨ=ΨΦΦΨ=ΦΨ=
Ô
( )
−εα−= 0
T
0
22 EtdtJ E0 = given fluence
with the constraints:
TDSE
[ ] ( ) ( )[ ] ( ) Ψμε−+−∂ι−χ−=χΨεT
0
t3 t tVT tdtIm2,,J
For given target state Φf , maximize the functional:
Optimal control of static targets(standard formulation)
( ) ( ) ( ) ( ) ( )TOTTTTJ f f 2
f 1 ΨΨ=ΨΦΦΨ=ΦΨ=
Ô
( )
−εα−= 0
T
0
22 EtdtJ E0 = given fluence
with the constraints:
TDSE
[ ] ( ) ( )[ ] ( ) Ψμε−+−∂ι−χ−=χΨεT
0
t3 t tVT tdtIm2,,J
For given target state Φf , maximize the functional:
GOAL: Maximize J = J1 + J2 + J3
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Control equations
1. Schrödinger equation with initial condition:
2. Schrödinger equation with final condition:
3. Field equation:
ˆ( ) ( ) ( ), (0)ti t H t tψ ψ ψ φ∂ = =
ˆˆ( ) ( ) ( ), ( ) ( )ti t H t t T O Tχ χ χ ψ∂ = =
1ˆ( ) Im ( ) ( )t t tε χ μ ψ
α=
0Jχδ = →
0Jψδ = →
0Jεδ = →
Set the total variation of J = J1 + J2 + J3 equal to zero:
Algorithm
Forward propagation
Backward propagation
New laser field
Algorithm monotonically convergent: W. Zhu, J. Botina, H. Rabitz,J. Chem. Phys. 108, 1953 (1998))
Quantum ring: Control of circular current
TDSE:
30 nm
1
1.04
1.12
1.24
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Control of currents|ψ(t)|
l = -1 l = 1
l = 0
|ψ(t)|2 j (t)j and
I ~ μA
E. Räsänen, A. Castro, J. Werschnik, A. Rubio, E.K.U.G., PRL 98, 157404 (2007)
OCT of ionization
• Calculations for 1-electron system H2+ in 3D
• Restriction to ultrashort pulses (T<5fs)
nuclear motion can be neglected
• Only linear polarization of laser (parallel or
perpendicular to molecular axis)
• Look for enhancement of ionization by pulse-shaping
only, keeping the time-integrated intensity (fluence)
fixed
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Control target to be maximized:
( ) ( )1ˆJ T O T= Ψ Ψ
with ϕϕ−=bound
iii1O
Standard OCT algorithm (forward-backward propagation) does notconverge:
Acting with before the backward-propagation eliminates the smooth(numerically friendly) part of the wave function.
O
Instead of forward-backward propagation, parameterize the laser pulse to beoptimized in the form
( ) ( ) ( )0t cot s t ,∈ = ωf
( ) ( ) ( )N
n nn
n1
n
2 2cos t sin t ,
T Tt
=
= ω + ω
f f g
Maximize J1 (f1…fN, g1…gN) directly with constraints:
( ) ( ) ( )
( )
N
nn 1
T 200
i f 0 f T 0 f 0
ii dt (t) E .
=
= = =
ε =
using algorithm NEWUOA (M.J.D. Powell, IMA J. Numer. Analysis 28, 649 (2008))
with ωn = 2πn/T
with ω0 = 0.114 a.u. (λ = 400 nm)
Choose N such that maximum frequency is 2ω0 or 4ω0 . T is fixed to 5 fs.
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Ionization probability for the initial (circles) and the optimized (squares) pulse as function of the peak intensity of the initial pulse. Pulse length and fluence is kept fixed during the optimization.
of initial pulse of initial pulse
• Formally the same OCT equations
• Problem: For 3 or more degrees of freedom, the full solution of the TDSE becomes computationally very hard
Control of many-body systems
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• Formally the same OCT equations
• Problem: For 3 or more degrees of freedom, the full solution of the TDSE becomes computationally very hard
Control of many-body systems
Instead of solving the many-body TDSE, combine OCT with TDDFTA. Castro, J. Werschnik, E.K.U. Gross, PRL 109, 153603 (2012)
• Formally the same OCT equations
• Problem: For 3 or more degrees of freedom, the full solution of the TDSE becomes computationally very hard
Control of many-body systems
Instead of solving the many-body TDSE, combine OCT with TDDFTA. Castro, J. Werschnik, E.K.U. Gross, PRL 109, 153603 (2012)
Important: Control target must be formulated in terms ofthe density!
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Enhancement of a single harmonic peak
Harmonic Spectrum:
( ) ( )2
2i t 3
t
dH dte d r r, t
dtω ω =
ρ
z
Maximize:
To maximize, e.g., the 7th harmonic of ω0 , choose coefficients asα7= 4, α3 = α5 = α9 = α11 = -1
[ ]( )
0 0k
k ,kk
F max Hω∈ ω −β ω +β
= α ω
( ) ( )ref 0
2t Tt cos cos t
2 T
π − ε = ε ω
[ ] ( )( )
0 0j , j
jref 0
max H
H jω∈ ω −β ω +β ω
κ =ω
Measure of enhancement: Compare with reference pulse:
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Harmonic spectrum of reference pulse for hydrogen atom
Results for Hydrogen
A. Castro, A. Rubio, E.K.U.Gross,arXiv:1409.4070,to appear in EPJ B (2015).
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Results for Helium
(Using TDDFT with EXX functional)
A. Castro, A. Rubio, E.K.U.Gross,arXiv:1409.4070, to appear in EPJ B (2015).
Lecture Notes in Physics 706(Springer, 2006)
Lecture Notes in Physics 837(Springer, 2012)