2014 L017 CECAMabinit14.sciencesconf.org/conference/abinit14/... · Institute of Condensed Matter...

transcript

Institute of Condensed Matter and Nanosciences,B-1348 Louvain-la-Neuve, Belgique

European Theoretical Spectroscopy Facility

Gian-Marco Rignanese

CECAM Tutorial: “Dynamical, dielectric and magnetic properties of solids with ABINIT”Lyon, 12-16 may 2014

Basics of density functional perturbation theory

CECAM Tutorial, Lyon, 12-16 may 2014

• Quantum treatment for electrons → Kohn-Sham equation

• Classical treatment for nuclei → Newton equation

Born-Oppenheimer approximation

atom direction (α=1,2,3)

unit cell

2—2 +Vext(r)+VHxc(r)

yi(r) = eiyi(r)

ka = ∂E

Eel [r] = Âvyv |T +Vext |yv+EHxc[r]

r(r) = Âv

yv (r)yv(r)

Raκα

= Raα+ τκα +u

Etot (u) = E(0)tot + ∑

aκα∑

a′κ ′α ′

∂ 2Etot

∂uaκα ∂ua′

κ ′α ′

uaκα u

κ ′α ′

Harmonic approximation

cell equilibrium atomic

position

displacement

• The matrix of interatomic force constants (IFCs) is defined as

• Its Fourier transform (using translational invariance)allows one to compute phonon frequencies and eigenvectors as solutions of the following generalized eigenvalue problem:

Phonons

phonon displacement

pattern

masses square of phonon

frequencies

Cκα ,κ ′α ′(a,a′) =

∂ 2Etot

∂uaκα ∂ua′

κ ′α ′

Cκα ,κ ′α ′(q) = ∑a′

Cκα ,κ ′α ′(0,a′)eiq·Ra′

Âk 0a 0

Cka,k 0a 0(q)Umq(k 0a 0) = Mk w2mqUmq(ka)

Example: Diamond

Theory vs. Experiment [X. Gonze, GMR, and R. Caracas, Z. Kristallogr. 220, 458 (2000)]

Total energy derivatives

• In fact, many physical properties are derivatives of the total energy (or a suitable thermodynamic potential) with respect to external perturbations.

• Possible perturbations include: atomic displacements, expansion or contraction of the primitive cell, homogeneous external field (electric or magnetic), alchemical change ...

• Related derivatives of the total energy (Eel + Eion) 1st order: forces, stress, dipole moment, ... 2nd order: dynamical matrix, elastic constants, dielectric

susceptibility, Born effective charge tensors, piezoelectricity, internal strains

3rd order: non-linear dielectric susceptibility, phonon-phonon interaction, Grüneisen parameters, ...

• Further properties can be obtained by integration over phononic degrees of freedom (e.g., entropy, thermal expansion, ...)

• These derivatives can be obtained from direct approaches: finite differences (e.g. frozen phonons) molecular-dynamics spectral analysis methods

perturbative approaches

• The former have a series of limitations (problems with commensurability, difficulty to decouple the responses to perturbations of different wavelength, ...). On the other hand, the latter show a lot of flexibility which makes it very attractive for practical calculations.

OutlinePerturbation Theory

Density Functional Perturbation Theory

Atomic displacements and homogeneous electric field

• Let us assume that all the solutions are known for a reference system for which the one-body Schrödinger equation is:

with the normalization condition:

• Let us now introduce a perturbation of the external potential characterized by a small parameter λ:

known at all orders.

Reference and perturbed systems

H(0)y(0)

E= e(0)i

Vext(λ ) =V(0)ext +λV

(1)ext +λ 2

V(2)ext + · · ·

• We now want to solve the perturbed Schrödinger equation:

with the normalization condition:

• Idea: all the quantities (X=H, εi, ψi) are written as a perturbation series with respect to the parameter λ :

Reference and perturbed systems

X(λ ) = X(0) +λX

(1) +λ 2X(2) +λ 3

X(3) + · · ·

with X (n) =1n!

dnXdl n

H(l )|yi(l )= ei(l )|yi(l )

yi(l )|yi(l )= 1

• Starting from:

and inserting:

we get:

Expansion of the Schrödinger equation

H(l )|yi(l )= ei(l )|yi(l ) l

yi(l ) = y(0)i +ly(1)

i +l 2y(2)i + . . .

ei(l ) = e(0)i +le(1)i +l 2e(2)i + . . .

H(! ) = H(0) +!H(1) +! 2H(2) + . . .

H(0) +!H(1) +! 2H(2) + . . .

i +! |"(1)i +! 2|"(2)

i + . . .=

#(0)i +!#(1)i +! 2#(2)i + . . .

i +! |"(1)i +! 2|"(2)

i + . . .

• This can be rewritten as:

setting λ=0

deriving w.r.t. λ and setting λ=0

deriving twice w.r.t. λ and setting λ=0

H(0)|y(0)i

H(0)|y(1)i +H(1)|y(0)

H(0)|y(2)i +H(1)|y(1)

i +H(2)|y(0)i

+ . . . =

e(0)i |y(0)i

e(0)i |y(1)i + e(1)i |y(0)

e(0)i |y(2)i + e(1)i |y(1)

i + e(2)i |y(0)i

+ . . .

• Finally, we have that:

0th order

1st order

2nd order

H(0)|!(0)i = "(0)i |!(0)

H(0)|!(1)i +H(1)|!(0)

i = "(0)i |!(1)i + "(1)i |!(0)

H(0)|!(2)i +H(1)|!(1)

i +H(2)|!(0)i =

"(0)i |!(2)i + "(1)i |!(1)

i + "(2)i |!(0)i

· · ·

• Starting from:

and inserting:

we get:

Expansion of the normalization condition

yi(l )|yi(l )= 1 l

yi(l ) = y(0)i +ly(1)

i +l 2y(2)i + . . .

y(0)i |y(0)

i |y(1)i + y(1)

i |y(0)i

+l 2y(0)

i |y(2)i + y(1)

i |y(1)i + y(2)

i |y(0)i

+ . . . = 1

• Finally, we have that

Expansion of the normalization condition

0th order

1st order

2nd order

y(0)i |y(0)

y(0)i |y(1)

i + y(1)i |y(0)

y(0)i |y(2)

i + y(1)i |y(1)

i + y(2)i |y(0)

· · ·

• Starting from the 1st order of the Schrödinger equation

and premultiplying by , we get:

and thus, finally, we have the Hellman-Feynman theorem:

• The 0th order wavefunctions are thus the only required ingredient to obtain the 1st order corrections to the energies.

1st order corrections to the energies

H(0)|y(1)i +H(1)|y(0)

i = e(0)i |y(1)i + e(1)i |y(0)

y(0)i |

y(0)i |H(0)|y(1)

i + y(0)i |H(1)|y(0)

i = e(0)i y(0)i |y(1)

i + e(1)i y(0)i |y(0)

e(1)i = y(0)i |H(1)|y(0)

| z e(0)i y(0)

i |y(1)i

• Starting from the 2nd order of the Schrödinger equation

and thus, finally, we have:

2nd order corrections to the energies

y(0)i |

| z e(0)i y(0)

i |y(2)i

H(0)|!(2)i +H(1)|!(1)

i +H(2)|!(0)i =

"(0)i |!(2)i + "(1)i |!(1)

i + "(2)i |!(0)i

!(0)i |H(0)|!(2)

i + !(0)i |H(1)|!(1)

i + !(0)i |H(2)|!(0)

"(0)i !(0)i |!(2)

i + "(1)i !(0)i |!(1)

i + "(2)i !(0)i |!(0)

!(2)i = "(0)i |H(2)|"(0)

i + "(0)i |H(1) !(1)i |"(1)

• Since the energies are real, we can write that:

or, combining both equalities:

• Using the expansion of the normalization condition at 1st order, we can finally write that:

• To obtain the 2nd order corrections to the energies, the only required ingredients are the 0th and 1st order wavefunctions.

!(2)i = "(0)i |H(2)|"(0)

i + "(0)i |H(1) !(1)i |"(1)

= "(0)i |H(2)|"(0)

i + "(1)i |H(1) !(1)i |"(0)

!(2)i ="(0)i |H(2)|"(0)

i |H(1) !(1)i |"(1)i + "(1)

i |H(1) !(1)i |"(0)i

!(2)i = "(0)i |H(2)|"(0)

i + 12

i |H(1)|"(1)i + "(1)

i |H(1)|"(0)i

• The 1st order of the Schrödinger equation

can be rewritten gathering the terms containing :

producing the so-called Sternheimer equation.

• In order to get one would like to invert theoperator, but it cannot be done as such since is an eigenvalue of . The problem can be solved by expressing the 1st order wavefunction as a linear combination of the 0th order ones:

1st order corrections to the wavefunctions

H(0)|y(1)i +H(1)|y(0)

i = e(0)i |y(1)i + e(1)i |y(0)

H(0) e(0)i

H(1) e(1)i

i |y(1)

|y(1)i (H(0) e(0)i )

|y(1)i = Â

jc(1)i j |y(0)

• We separate the 0th order wavefunctions into two subsets: those associated to :

(just if the energy is non-degenerate) those that belong to the subspace that is orthogonal: j ∈ I⊥

• The Sternheimer equation can thus be rewritten as:

e(0)i|y(0)

i j I if H(0)|y(0)

j = e(0)i |y(0)j

|y(1)i = Â

jc(1)i j |y(0)

j = ÂjI

c(1)i j |y(0)j + Â

jIc(1)i j |y(0)

H(0) e(0)i

i = Âj

c(1)i j

H(0) e(0)i

= ÂjI

c(1)i j

e(0)j e(0)i

H(1) e(1)i

• Premultiplying by with k ∈ I⊥, we get:

and, thus:

c(1)i j

e(0)j e(0)i

k |y(0)j =y(0)

k |H(1) e(1)i |y(0)i

y(0)k |

| z δkj y(0)

k |y(0)i = 0

since k I

c(1)ik

e(0)k e(0)i

k |H(1)|y(0)i

c(1)i j =1

e(0)i e(0)j

y(0)j |H(1)|y(0)

i for j I

• Premultiplying by with k ∈ I, we get:

• For k = i, it is nothing but the Hellmann-Feynman theorem.But, it does not provide any information on the .

• In fact, there is a gauge freedom that allows to choose them equal to zero.

c(1)i j

e(0)j e(0)i

k |y(0)j =y(0)

k |H(1) e(1)i |y(0)i

y(0)k |

| z 0 y(0)

k |y(0)i = dki

since k I

c(1)i j for j 2 I

e(1)k dki = y(0)k |H(1)|y(0)

• Finally, we can write the so-called sum over states expression:

which requires the knowledge of all the 0th order wavefunctions and energies.

• Instead, if we define the projector

we can rewrite the Sterheimer equation in that subspace:

PI? onto the subspace I? by:

PI = ÂjI

|y(0)j y(0)

H(0) e(0)i

(1)i =PIH(1)|y(0)

|y(1)i = Â

jI|y(0)

e(0)i e(0)j

y(0)j |H(1)|y(0)

• In this form, the singularity has disappeared and it can thus be inverted:

and defining the Green’s function in the subspace as:

we can write:

• This is the Green's function technique for dealing with the Sternheimer equation.

PI |y(1)i =

H(0) e(0)i

i1H(1)|y(0)

PI |y(1)i = GI(e

(0)i )H(1)|y(0)

GI?(e) =hPI?

e H(0)

• The sum over states expression for the 1st order wavefunctions:

can be inserted in the 2nd order corrections to the energies:

leading to:

|y(1)i = Â

jI|y(0)

e(0)i e(0)j

y(0)j |H(1)|y(0)

!(2)i = "(0)i |H(2)|"(0)

i + 12

i |H(1)|"(1)i + "(1)

i |H(1)|"(0)i

!(2)i ="(0)i |H(2)|"(0)

"(0)i |H(1)|"(0)

j 1!(0)i !(0)j

"(0)j |H(1)|"(0)

• Alternatively, we can write that:

and the perturbation expansion at the 2nd order gives:

• It can be shown that the sum of the terms in a row or in column vanishes! Getting rid of the first row and the last column, we get another expression for the 2nd order corrections to the energies:

!i(" )|H(" ) #i(" )|!i(" )= 0 "

!(0)i |H(0) "(0)i |!(2)

i +!(0)

i |H(1) "(1)i |!(1)i +!(1)

i |H(0) "(0)i |!(1)i

+!(0)i |H(2) "(2)i |!(0)

i +!(1)i |H(1) "(1)i |!(0)

i +!(2)i |H(0) "(0)i |!(0)

!(2)i ="(0)i |H(2)|"(0)

i + "(1)i |H(0) !(0)i |"(1)

+ "(0)i |H(1) !(1)i |"(1)

i + "(1)i |H(1) !(1)i |"(0)

• Actually, a number of other expressions exist for the 2nd order corrections to the energies.

• However, it can be demonstrated that this expression is variational in the sense that the 2nd order corrections to the energies can be obtained by minimizing it with respect to :

under the constraint that:

!(2)i =min"(1)i

"(0)i |H(2)|"(0)

i + "(1)i |H(0) !(0)i |"(1)

+"(0)i |H(1) !(1)i |"(1)

i + "(1)i |H(1) !(1)i |"(0)

!(0)i |!(1)

i + !(1)i |!(0)

• Starting from the 3rd order of the Schrödinger equation

3rd order corrections to the energies

y(0)i |

| z !(0)i "(0)

i |"(3)i

H(0)|!(3)i +H(1)|!(2)

i +H(2)|!(1)i +H(3)|!(0)

"(0)i |!(3)i + "(1)i |!(2)

i + "(2)i |!(1)i + "(3)i |!(0)

!(0)i |H(0)|!(3)

i + !(0)i |H(1)|!(2)

+ !(0)i |H(2)|!(1)

i + !(0)i |H(3)|!(0)

= "(0)i !(0)i |!(3)

i + "(1)i !(0)i |!(2)

+ "(2)i !(0)i |!(1)

i + "(3)i !(0)i |!(0)

• Finally, we we can write:

• This expression of the 3rd order corrections to the energies requires to know the wavefunctions up to the 2nd order.

!(3)i ="(0)i |H(3)|"(0)

+ "(0)i |H(2) !(2)i |"(1)

+ "(0)i |H(1) !(1)i |"(2)

• Alternatively, we can write that:

and the perturbation expansion at the 3rd order gives:

• Again, the sum of the terms in a row or in column vanishes. So, getting rid of the first two rows and the last two columns, we get another expression that does not require to know the 2nd order wavefunctions :

!i(" )|H(" ) #i(" )|!i(" )= 0 "

!(0)i |H(0) "(0)i |!(3)

i +!(0)

i |H(1) "(1)i |!(2)i +!(1)

i |H(0) "(0)i |!(2)i

+!(0)i |H(2) "(2)i |!(1)

i +!(1)i |H(1) "(1)i |!(1)

i +!(2)i |H(0) "(0)i |!(1)

i +!(0)

i |H(3) "(3)i |!(0)i +!(1)

i |H(2) "(2)i |!(0)i +!(2)

i |H(1) "(1)i |!(0)i +!(3)

i |H(0) "(0)i |!(0)i = 0

!(3)i ="(0)i |H(3)|"(0)

i + "(1)i |H(1) !(1)i |"(1)

+ "(0)i |H(2)|"(1)

i + "(1)i |H(2)|"(0)

• There are 4 different methods to get the 1st order wavefunctions: solving the Sternheimer equation directly, complemented by a

condition derived from the normalization requirement using the Green’s function technique exploiting the sum over states expression minimizing the constrained functional for the 2nd order

corrections to the energies

• With these 1st order wavefunctions, both the 2nd and 3rd order corrections to the energies can be obtained.

• More generally, the nth order wavefunctions give access to the (2n)th and (2n+1)th order energy [“2n+1” theorem].

Summary

• In DFT, one needs to minimize the electronic energy functional:

in which the electronic density is given by:

• Alternatively, one can solve the reference Shrödinger equation:

where the Hartree and exchange correlation potential is:

Reference system

V (0)Hxc(r) =

dE(0)Hxc[r(0)]

r(0)(r) =Ne

i (r)i

y(0)i (r)

Eel [r(0)] =Ne

T +V (0)ext

E+E(0)

Hxc[r(0)]

E= di j

H(0)y(0)

2—2 +V (0)

ext +V (0)Hxc

E= e(0)i

• The electronic energy functional to be minimized is:

in which the electronic density is given by:

• Alternatively, the Shrödinger equation to be solved is:

where the Hartree and exchange correlation potential is:

Perturbed system

r(r;l ) =Ne

yi (r;l )yi(r;l )

yi(l )| y j(l )↵= di j

H(l ) |yi(l )=1

2—2 +Vext(l )+VHxc(l )

|yi(l )= ei(l ) |yi(l )

VHxc(r;l ) = dEHxc[r(l )]dr(r)

Eel [r(l )] =Ne

yi(l ) |T +Vext(l )|yi(l )+EHxc[r(l )]

1st order of perturbation theory in DFT

• For the energy, it can be shown that:

This is the equivalent of the Hellman-Feynman theorem for density-functional formalism.

• For the wavefunctions, the constraint leads to:

E(1)el =

(T +Vext)(1)y(0)

EHxc[r(0)]l=0

2nd order energy in DFPT

• For the energy, it can be shown that:

E(2)el =

hDy(1)

(T +Vext)(1)y(0)

(T +Vext)(1)y(1)

hDy(0)

(T +Vext)(2)y(0)

(H ei)(0)y(1)

Z Z d 2EHxc[r(0)]

dr(r)dr(r0)r(1)(r)r(1)(r0)drdr0

dlEHxc[r(0)]

r(1)(r)dr+ 12

dl 2 EHxc[r(0)]l=0

r(1)(r) =Ne

i (r)i

y(0)i (r)+

i (r)i

y(1)i (r)

1st order wavefunctions in DFPT

• The 1st order wavefunctions can be obtained by minimizing:

with respect to under the constraint:

• These can also be obtained by solving the Sternheimer equation:

E(2)el = E(2)

o Dy(0)

H(0) e(0)i

H(1) e(1)i

H(1) = (T +Vext)(1) +

Z d 2EHxc[r(0)]

dr(r)dr(r0)r(1)(r0)dr0

e(1)i = y(0)i |H(1)|y(0)

Higher orders in DFPT

• More generally, it easy to show that since there is a variational principle for the 0th order energy:

non-variational expression can be obtained for higher orders:

• But, this is not the best that can be done!

E(0)el = E(0)

E(1)el = E(1)

E(2)el = E(2)

E(3)el = E(3)

· · ·

• We assume that all wavefunctions are known up to (n-1)th order:

• The variational property of the energy functional implies that:

• Taking , we see that:

if the wavefunctions are known up to (n-1)th order,the energy is know up to (2n-1)th order;

if the wavefunctions are known up to nth order,the energy is know up to (2n+1)th order.

• This is the “2n+1” theorem.

yi = y<ni +O(l n) = y(0)

i +ly(1)i + · · ·+l n1y(n1)

i +O(l n)

ytrial=

and h = l nEel [ytrial +O(h)] = Eel [ytrial]+O(h2)

• Since the variational principle is also an extremal principle[the error is either > 0 → minimal principle, or < 0 → maximal principle], the leading missing term is also of definite sign (it is also an extremal principle):

E(0)el = E(0)

variational w.r.t.

E(1)el = E(1)

E(2)el = E(2)

variational w.r.t.

E(3)el = E(3)

E(4)el = E(4)

variational w.r.t.

E(5)el = E(5)

· · ·

• Similar expressions exist for mixed derivatives (related to two different perturbations j1 and j2):

• The extremal principle is lost but the expression is stationary: the error is proportional to the product of errors made in the

1st order quantities for the first and second perturbations; if these errors are small, their product will be much smaller; however, the sign of the error is undetermined, unlike for the

variational expressions.

Mixed derivatives in DFPT

E j1 j2el = E j1 j2

y(0)i ;y j1

i ;y j2i

1. Ground state calculation:

2. FOR EACH pertubation j1 DO

3. FOR EACH pertubation pair j1, j2 DO

determine using both (stationary expression)

using just ENDDO

4. Post-processing to get the physical properties from

Order of calculation in DFPT

(0)ext

! y(0)i

and r(0)

y(0)i and r(0)

! y j1i

and r j1

E j1 j2

minimize 2nd order energy solve Sternheimer equation

E j1 j2

y j1i and y j2

Perturbations of the periodic solid

• Let us consider the case where the reference system is periodic:

• It can be shown that if the perturbation is characterized by a wavevector q such that:

all the responses, at linear order, will also be characterized by q:

(0)ext

(1)ext

iq·Ra

(1)ext

r(1)(r+Ra) = eiq·Rar(1)(r)

y(1)i,k,q(r+Ra) = eiq·Ray(1)

i,k,q(r)

· · ·

Perturbations of the periodic solid

• We define related periodic quantities:

• In the equations of DFPT, only these periodic quantities appear: the phases can be factorized.

• The treatment of perturbations incommensurate with the unperturbed system periodicity is mapped onto the original periodic system.

• This is interesting for atomic displacements but more importantly for electric fields.

r(1)(r) = eiq·rr(1)(r)

u(1)i,k,q(r) = (Ne W0)1/2ei(k+q)·Ry(1)

i,k,q(r)

eiq·r and ei(k+q)·R

Electronic dielectric permittivity tensor

• The dielectric permittivity tensor is the coefficient of proportionality between the macroscopic displacement field and the macroscopic electric field, in the linear regime:

• At high frequencies of the applied field, the dielectric permittivity tensor only includes a contribution from the electronic polarization:

48unit vector

Dmac,a = Âa 0

eaa 0Emac,a 0

ε∞αα ′ = δαα ′ −

2EE ∗

α Eα ′

∑αα ′

qα ε∞αα ′ q

ε−1

G=0,G′=0(q → 0)

eaa 0 =∂Dmac,a∂Emac,a 0

= daa 0 +4p∂Pmac,a∂Emac,a 0

Treatment of homogeneous electric fields

• When the perturbation is an electric field, we have:

which breaks the periodic boundary conditions.

• To obtain the 2nd order derivative of the energy:

the following matrix elements need to be computed:

2EE a Ea 0

rEa 0 (r)ra dr

Du(0)c,k

uEav,k

u(0)v,k

conduction valence

(1)ext

(r) = E · r

Treatment of homogeneous electric fields

• These matrix elements can be determined writing that:

which leads to the Sternheimer equation:

e(0)i,k e(0)j,k

Du(0)i,k

u(0)j,k

u(0)i,k

H(0)kk ra ra H(0)

u(0)j,k

u(0)i,k

i∂H(0)

kk∂ka

u(0)j,k

kk e(0)j,k

u(0)j,k

E=Pc i

∂H(0)kk

u(0)j,k

H(0) e(0)i

(1)i =PIH(1)|y(0)

DDK perturbation

• It is defined as the proportionality coefficient relating at linear order, the polarization per unit cell, created along the direction α, and the displacement along the direction α’ of the atoms belonging to the sublattice κ:

• It also describes the linear relation between the force in the direction α’ on an atom κ and the macroscopic electric field

• Both can be connected to the mixed 2nd order derivative of the energy with respect to uκα’ and Eα

• Sum rule:

Born effective charge tensor

καα ′ = Ω0

∂Pmac,α

∂uκα ′(q = 0)

=∂Fκα ′

∂Eα

uκα ′=0

καα ′ = 0

Born effective charge tensor

• Model system: diatomic molecule: dipole moment related to static charge q(r): 𝒫(r)= q(r) r

• Atomic polar charge Z*(r) such that ∂𝒫(r)= Z*(r)∂r purely covalent case: q(r)=0=Z*(r) purely ionic case: q(r)=Q ≠ 0 ⇒Z*(r)=Q mixed ionic-covalent: ∂𝒫(r)= q(r)∂r + ∂q(r) r

+q(r)-q(r)r

𝒫(r)

Z*(r) Q

Static dielectric permittivity tensor

• The mode oscillator strength tensor is defined as

• The macroscopic static (low-frequency) dielectric permittivity tensor is calculated by adding the ionic contribution to the electronic dielectric permittivity tensor:

Sm,αα ′ =

∑κβ

καβU∗

mq=0(κβ )

∑κβ ′

κα ′β ′Umq=0(κβ ′)

εαα ′(ω) = ε∞αα ′ +

Ω0∑m

Sm,αα ′

ω2m −ω2

αα ′ = ε∞αα ′ +

Ω0∑m

Sm,αα ′

LO-TO splitting

• The macroscopic electric field that accompanies the collective atomic displacements at q → 0 can be treated separately:

where the nonanalytical, direction-dependent term is:

• The transverse modes are common to both C matrices but the longitudinal ones may be different, the frequencies are related by

Cκα ,κ ′α ′(q → 0) = Cκα ,κ ′α ′(q = 0)+CNA

κα ,κ ′α ′(q → 0)

κα ,κ ′α ′(q → 0) =4π

∑β qγ Z∗

κβα

∑′

β q′β Z∗

κ ′β ′α ′

∑ββ ′ qβ ε∞ββ ′q

ω2m(q → 0) = ω2

m(q = 0)+4π

∑αα ′ qα Sm,αα ′q′α

∑αα ′ qα ε∞αα ′q′α

0 200 400 600 800 1000 1200

Experimental frequency (cm1)

lative

PBEsol

0 200 400 600 800 1000 12000

Experimental frequency (cm−1)

(cm−1

LDAPBEPBEsolAM05WCHTBS

Example 1: Zircon (phonons)

Example 1: Zircon (Born effective charges)

• M : anomalously large (esp. Z⊥) → PbZrO3, ZrO2

• Si : smaller deviations ( and ) → SiO2 (α-quartz or stishovite)

• O : strong anisotropy → SiO2 stishovite or TiO2 rutile in the y-z plane (plane of the M-O bonds) (rem: ≠ from SiO2 α-quartz in the x direction where 2 components)

Interpretation:• mixed ionic-covalent bonding

• closer to stishovite than α-quartz in agreement with naive bond counting for O atoms

Nominal: M → +4 Si → +4 O → -2

Example 1: Zircon (dielectric properties)

• due to the frequency factor, it is the lowest frequency mode that contributes the most to ε0

• Sm and Zm are the largest for the lowest and highest frequency modes*

• this effect can be compensated by a lower frequency for hafnon [e.g. A2u(1)]

• Sm and Zm are smaller for HfSiO4 ← mass difference and Born effective charges*

Γ X W L Γ K X

Example 2: Copper (thermodynamics)

0 200 400 600 800 1000

PBEsol

0 200 400 600 800 1000

PBEsol

0 200 400 600 800 1000

PBEsol

0 200 400 600 800 1000

PBEsol

0 200 400 600 800 1000

PBEsol

0 200 400 600 800 1000

PBEsol

• S. Baroni, P. Giannozzi & A. Testa, Phys. Rev. Lett. 58, 1861 (1987) • X. Gonze & J.-P. Vigneron, Phys. Rev. B 39, 13120 (1989) • X. Gonze, Phys. Rev. A 52 , 1096 (1995) • S. de Gironcoli, Phys. Rev. B 51, 6773 (1995) • X. Gonze, Phys. Rev. B. 55, 10337 (1997) • X. Gonze & C. Lee, Phys. Rev. B. 55, 10355 (1997) • S. Baroni, S. de Gironcoli, A. Dal Corso, P. Giannozzi,

Rev. Mod. Phys. 73, 515 (2001)

2014 L017 CECAMabinit14.sciencesconf.org/conference/abinit14/... · Institute of Condensed Matter...

Documents