excited state properties: electronic and optical ...nano-bio.ehu.es/files/2-spectroscopies.pdf ·...
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Excited state properties: electronic and optical
spectroscopies
Dott.ssa Letizia ChiodoNano-bio Spectroscopy Group &
ETSF - European Theoretical Spectroscopy Facility,Dipartemento de Física de Materiales, Facultad de Químicas,
Universidad del País Vasco UPV/EHU, San Sebastián-Donostia, Spain
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Outline of the Lectures
• Many Body Problem• DFT elements; examples• DFT drawbacks• excited properties:
electronic and optical spectroscopies. elements of theory• Many Body Perturbation Theory: GW• codes, examples of GW calculations• Many Body Perturbation Theory: BSE• codes, examples of BSE calculations• Time Dependent DFT• codes, examples of TDDFT calculations• state of the art, open problems
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Outline
• DFT drawbacks• Photoemission Spectroscopy• Electron Energy Loss Spectroscopy• Optical absorption
• Polarizability• Screening• Random Phase Approximation• Local Field Effects
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DFT drawbacks
We have detected two problems with DFT:1) Kohn-Sham bandgaps are much too small2) Fermi’s golden rule in the independent particle picture is not reliableto calculate absorption spectraHow can we understand this?
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DFT drawbacks
We have detected two problems with DFT:1) Kohn-Sham bandgaps are much too small2) Fermi’s golden rule in the independent particle picture is not reliableto calculate absorption spectraHow can we understand this?
L. Chiodo et al., phys. stat. sol. (b) 242, No. 15, 3032–3039 (2005)
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Kohn-Sham bandgaps
DFT is a ground state theory:KS LUMO-HOMO is not the gap!!!!KS-gap is strongly underestimated for 2 reasons
Vxc discontinuosVxc not exact
adapted from M. van Schilfgaarde et al., PRL 96 226402 (2006)
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Kohn-Sham bandgaps
KS eigenvalues are obtained as Lagrange multipliers, cannot be interpreted as removal/addition energies: Koopman’s theorem doesn’t hold
to calculate the electronic gap, we can use two calculations of the Kohn-Sham HOMO energy, one for the N-particle system and another for the N+1-particleand then apply the ionization potential theorems of KS-DFT the gap is exact if the exact XC potential is used to calculatethese quantitiesthis because of the discontinuity of the exchange-correlation potential as theparticle number is varied across an integer
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Optical Absorption
quantitatively and often qualitatively wrong
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other problems…
LDA(GGA) gives: wrong ground state for the titanium atomwrong magnetic ground state for bulk ironwrong adsorption energy of CO on metal surfaces
LDA, due to its local character, cannot describe van der Waals and hydrogen bonding………..
use of different Vxc can improve e.g. structural results for large organic molecules(isomers), but cannot correct the Vxc discontinuity, due to the GS nature of DFT
we are describing states that are not GROUND STATES, but EXCITED STATES therefore not included in DFT
moreover, how to relate macroscopic (experiment) and microscopic (ab initio) world?
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Experimental Techniques
to understand and correct the errors we are doing in DFT, it is usefull tounderstand the experimental techniques giving us the excited state properties wewant to study
between Electronic Excitations, there are
•Photoemission Spectroscopy•Inverse Photoemission Spectroscopy•Electron Energy Loss Spectroscopy•Optical Absorption•Inelastic X-ray Scattering
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Photoemission Spectroscopy
UPS,XPS,ARPES, ARIPES
UPS � density of statesAR-UPS � band structure (valence)AR-IPES � empty states (conduction
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Photoemission Spectroscopy
UPS,XPS,ARPES, ARIPES
UPS � density of statesAR-UPS � band structure (valence)AR-IPES � empty states (conduction
1 e- is removed (added), the system is charged, and in an excited state(easy for metals, more difficult for semiconductors and insulators)
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Electron Energy Loss Spectroscopy
energy-loss function, measured in EELS or IXSS, is related to minus the imaginary part of the inverse macroscopic dielectric function
}{ ),(),(EL 1 ωεω qq−−ℑ= M
dependence on the transferred momentum
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LEED
HREELS
EELS Auger
electron cascade
Electron Energy Loss Spectroscopy
energy-loss function, measured in EELS or IXSS, is related to minus the imaginary part of the inverse macroscopic dielectric function
}{ ),(),(EL 1 ωεω qq−−ℑ= M
dependence on the transferred momentum
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Optical Absorption
c
ex x
νωεα
α
2
0I)(I
=
= −
}{ ),0()(ABS ωεω →ℑ= qM
optical transitions: transferred momentum is 0
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from Macro (experiments, Maxwell equations) to micro (ab initio): averaging procedure
be careful with symmetries of the studied sample (cubic, not cubic, etc…)
differences between the microscopic fields and the averaged (macroscopic) fields:crystal local fields (due to local fluctuations at micro scale)
microscopic dielectric functions are determined by the elementary medium excitations interband and intraband transitions, as well as collective excitations
Micro-Macro
N.B real and reciprocal space are both present in all the following theoryand codes implementation
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Polarizabilityχε v11 +=−
∑ +−−−=
ij ji
jiji
jii
ffηεεω
φφφφχ
)(
)'()'()()()(
**
0rrrr
single particle polarizability RPAe-
h+
c
v
ωcvhν
P =
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Polarizability
F. Sottile, Ph.D. thesis, 2003
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Screeningfrom polarizability �microscopic dielectric function χε v11 +=−
observable quantities and spectra are related to the macroscopic dielectric function εMobtained from the microscopic ε by spatially averaging over a distance large enough with respect to the microscopic structure of the system, e.g. in solids an elementary cell
),',(),',( ωεωε rrrrM =
),(),(),(
1),( 0',01
0',0
ωεωεωε
ωε qqq
q NLF
MGG
GG
M =≠= ==−==
if microscopic dielectric matrix contains off-diagonal terms
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Screening and LFEcrystal local-field effects are neglected
• absent in the homogeneous electron gas • marginal in weakly inhomogeneous systems (e.g silicon)• important in systems presenting strong inhomogeneities in the electronic density
in particular, local-field effects are critical in reduced dimensionality systems 2D surfaces/graphene1D nanotubes/wires0D clusters and molecules
),(),(0',0 ωεωε qq NLF
MGG ===
L. Chiodo et al., phys. stat. sol. (b) 242, No. 15, 3032–3039 (2005)
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Local Field Effects: NWs of Ge
left panels: light polarized along the wire axis xright panels: light polarized perpendicularly to the axis yM. Bruno, et al., Phys. Rev. B 72, 153310 (2005)
LFE: source ofanisotropy in response function
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LFE in EELS: zirconia
theoretical dielectric function for c-ZrO2top panel, real partcenter panel, imaginary partbottom panel, the loss function
solid lines, RPA with local fields. dashed lines, without local fields.
L. K. Dash, et al., PRB 70, 245116 (2004)
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LFE in EELS: titania
Dynamical structure factor (top panel); macroscopic dielectric function (middle and bottom panels) of TiO2 along the [001] direction. The solid (dotted) line represents the calculated ALDA spectrum with (without) LFE. The dashed line denotes the calculated RPA result with LFE.
I. G. Gurtubay, et al., PRB 70, 201201(R) (2004)
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IP - Random Phase Approximation
RPAe-
h+
c
v
ωcvhν
P =
non interacting electron-hole pairs, without local field
( ) ( )ωεεδϕϕω
πωε −−= ∑ vc
cv
vcM v,
2
2
16Im Fermi Golden rule
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Anatase Titania Absorption Spectrum
we want to correct these spectra….
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DFT is the first step for excited state properties:
electronic properties (DOS, band structure, surface states),
dielectric response at RPA level
.....
local field effects play an important role, to improve properties
connected to screening (absorption, electron energy loss)
because they mix somehow the otherwise independent transitions
but they are not enough
how can we further improve results?
thanks toDr. Matteo GattiDr. Silvana Botti