oxides for thermoelectricity - ucsb mrsecseshadri/2012-summerschool-talks/ucsb-2012-hebert.pdf ·...
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Oxides for thermoelectricity
Sylvie HébertLaboratoire CRISMAT
UMR6508 CNRS et ENSICAEN
UCSB – ICMR Summer School on Inorganic Materialsfor Energy Conversion and Storage
August 2012
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Laboratoire CRISMATCristallographie et Sciences des Matériaux
Caen
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CRISMAT : some figures
120 persons 47 researchers 15 post-doc 42 Ph-D students 125 publications per year
Search for new oxides : high Tc superconductors, colossal magneto-resistance, thermoelectrics, multiferroics…
And Beyond oxides
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Thermoelectric Activities
7 permanent staff + 1 engineer + students / postdocs + the rest of the lab!
→ Synthesis / Processing
→ Low and high T thermoelectric properties
→ Modelization of the thermoelectric properties
→ Module and module testing
Ramzy Daou, Franck Gascoin, Christophe Goupil, Emmanuel Guilmeau, Sylvie Hébert, Antoine Maignan, Jacques Noudem
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TechniquesCristallography (8 diffractometers)
80 furnaces Thin-films (PLD’s)
5 TEM, 3 SEMthermomechanicaltests
+ SPS
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Low T properties
3 SQUID magnetometersHmax =5.5T
2K < T < 400K
4 ‘PPMS’Hmax = 14T
2K < T < 400K
DC and AC magnetization
DC and AC magnetizationMagnetization up to 1000K (VSM)
ResistivitySpecific heat
Seebeck coefficient Thermal conductivity
F. Janin, Photothèque CNRS
Thermopower and thermal conductivity measurements developped by Jiri Hejtmanek (Prague), using PPMS environment
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High T properties
ZT = 2T/
ZEM 3 Ulvac RikoCombined Seebeck and resistivity
measurement(RT to 700°C)
seebeck
Electrical resistivity
Thermal conductivity
= diffusivity x density x Cp
Netzsch
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Modules
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Oxides for thermoelectricity
• Introduction : Oxides specificities / Models for oxides /
Best thermoelectric oxides
• Semi – conductors : the Heikes formula• Degenerate semi-conductors : best n type oxides
• NaxCoO2 and misfit compounds
• Nanostructuration• Modules
• Conclusion
Aim of this tutorial : Best thermoelectric oxides /
show the specificities of oxides
Increaseof thecarrier density
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Introduction
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Property MaterialsMetals CrO2, Fe3O4, SrRuO3
Insulators Cr2O3, CoO, Fe2O3, Al2O3
Metal-Insulator Transition VO2, V2O3
Superconductors Ba(Bi,Pb)O3, YBa2Cu3O7
Piezo- and Ferroelectrics Pb(Zr,Ti)O3, BaTiO3
Catalysts (chemical, photo-) TiO2 , LaCoO3, BiMoO4
Ferro-, Antiferro-, Ferrimagnets CrO2, MnO, MnFe2O4
Pigments TiO2, CoAl2O4, Co3(PO4)2
Sensors CaxZr1-xO2-x, SnO2
Negative Thermal Expansion ZrW2O8
Ionic Conductors (battery, SOFC) LixMnO2, CaxZr1-xO2-x
Thermoelectrics NaxCoO2
Non-Linear Optics LiNbO3
Rutile, TiO2
YBa2Cu3O7
LiNbO3
LiMnO2
ZrW2O8
NaxCoO2
Why oxides?Strong interplay between spin/charge/lattice
Large family of compounds,Can be cheap, environment friendly and resistant in air
From M. Subramanian,OSU
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Specificities of oxidesHigh T synthesis and synthesis possible in oxydizing environment
Oxides can be stable at high T and in airNon toxic elements, abundance of elements…
Strong electronic correlations→ Difficult to calculate the band structure→ But could be interesting for the Seebeck!
Kinetic energy ~ Repulsive Coulomb energy
Strong renormalization of effective massesNarrow bands
D. Basov et al., Rev. Mod. Phys. 83, 471 (2011)A. Georges et al., Rev. Mod. Phys. 68, 13 (1996)
Introduction
Possible tuning of the electronic correlations
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A. Georges et al., Rev. Mod. Phys. 68, 13 (1996)
Influence of electronic correlations
U increasing
Modification of DOS→ Increase of S?
J. Merino et al., PRB61, 7996 (2000)
Calcul of U impact on theSeebeck coefficient
Introduction
DOS
SeebeckMetal
Insulator
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Bibliography : Thermoelectric oxides•First papers in the 60’s : SnO2, SbO2…
Degenerate n type semi-conductors
•1980’s : thermopower is used as a probe for the cuprates
•1990’s : Doped ZnO as best n type thermoelectric oxide (Ohtaki et al.)
•1997 : NaxCoO2 (Terasaki et al.)
Introduction
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PRB46, 14928 (1992)
Correlation between Seebeck / doping / Critical temperature
Introduction
High Tc superconductors
YBa2Cu3O7-
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M. Ohtaki et al., JAP79, 1816 (1996)
Zn1-xAlxO (x = 0 – 0.1)
Broadband model for extrinsic n type semiconductor
Large mobility of the carriers : 3 – 7cm2/Vs
= 40Wm-1K-1 at 300K=5.4 Wm-1K-1 at 1000°C
ZT = 0.3
But is too high !!!
Introduction
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Metallicity (crystals) ~ 0.2 m cmLarge S S ~ +80 V/KSmall (polycrystals) Wm
(crystals) ~ 5Wm-1K-1
Na0.7CoO2‘ Phonon Glass / Electron crystal ’
I. Terasaki et al., Phys. Rev. B 56, R12685 (1997)
Na0.7CoO2P= 50 10-4 WK-2m-1
Bi2Te3P= 40 10-4 WK-2m-1
At 300K
Power factor P=S2/ at 300K
Co3+ (3d6) / Co4+ (3d5)
NaxCoO2 : Na+xCo3+
xCo4+1-xO2 Measurements on polycrystals
Introduction
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ZT of oxides
p type :NaxCoO2, Misfitoxides
n type : TCOs
1992 1994 1996 1998 2000 2002 2004 2006 2008 20100.00.10.20.30.40.50.60.70.80.91.01.11.2
FujitaNa
xCoO
2
R. FunahashiCa
3Co
4O
9 Whisker
n-type Bulk p-type Bulk p-type single crystals
M.Ohtaki(Zn,Al,Ga)O
G. XuCa
3Co
4O
9
H. ItaharaCa
3Co
4O
9
R. FunahashiBiSrCoO
L. BoscherCa(Mn,Nb)O
3
D. BérardanGe:In
2O
3H. Kaga
ZnO-In2O
3M.Ohtaki(Zn,Al)O
M.OhtakiIn
2O
3-SnO
2
ZT
(10
00
K)
Year
2 different families for the best thermoelectric oxides• Type p : oxides related to NaxCoO2, metallic and large S
• Type n : ‘transparent conducting oxides’, degenerate semi-conductors
ZT (type p ) > ZT (type n)
Introduction
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High T properties of NaxCoO2
K. Fujita et al. JJAP40, 4644 (2001)
Introduction
Crystal and polycrystal measurements
Crystals : 1.5 ×1.5 × 0.03 mm3
ZT ~ 1 for crystals only at 800K
ZT = 1
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Oxides
MisfitsNaxCoO2Large S
+ metallic small p type
Model systemTexturation problems
Transparent conductors, DelafossitesLarge S, small
Large Mostly n type (some p type)
Reduction of through nanostructuration?
Semi-conductorsLarge
SLarge
n and p type Increase of S
through Heikes?
Introduction
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Modelization of thermoelectric propertiesin oxides
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)(
22
le
TSTSZT
•Mott’s formula :FEE
B
EET
ekS
))(ln(
3
22
(E) = en(E) (E)
Models
U increasingDOS
Seebeck
Possible increase of S due to strong correlations?
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)(
22
le
TSTSZT
(E)en(E)ρ 1 • Resistivity :
A large mobility is required (difficult for oxides!)
• Thermal conductivityElectronic part related to -1 (Wiedemann Franz), usually
smallLattice part has to be minimized
Models
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Models
)(3
/ 22
FBel ENkTC
FEEB
EET
ekS
))(ln(
3
22
Mott’s formula : influence of electronic correlations
K. Behnia et al. JPCM 16, 5187 (2004)
Free electron gas
Very similar to the electronic specific heat
Relationship between Seebeck and specific heat at low T??
is a probe of electronic correlations
Scattering parameter
Carrier density
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csteeNTSq Av
K. Behnia et al. JPCM 16, 5187 (2004)
Low T limit
2q5.0
Universal value for the ratio of S /
Limit T 0
)(3
/ 22
FBel ENkTC
Models
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The Heikes formula
P. M. Chaikin et al. Phys. Rev. B 13, 647 (1976)
Models
‘Simple combinatorial problem’
Calculated for organic thermoelectrics
High T limit
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The Heikes formula
Te/
TeS/S
S)1()2(
Hubbard model
S(1) , S(2) : depend on v and Q, velocity and energy operatorsValid for narrow band systems (localized correlated particles)
Limit T : S ~ entropy / carrier
for T
)x
x1ln(e
kS B
-0.4 -0.2 0.0 0.2 0.4-600
-400
-200
0
200
400
600
S(V
/K)
x
x = concentration of carriers
Holes
Electrons
P. M. Chaikin et al. Phys. Rev. B 13, 647 (1976)
Models
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0.0 0.2 0.4 0.6 0.8 1.0-300-200-100
0100200300400500600
Co3+ LS + Co4+ LS : =1/2
S Hig
hT(
V/K
)x
Extra term in the Heikes formula due to the spin degeneracy
Mixed valency cation Mn+ / M(n+1)+ :
Spin entropy
1S21S2
1n
n
J. P. Doumerc JSSC 110, 419 (1994)
)xx-1ln(
ekS B
S=0 S=1/2
Models
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0.0 0.2 0.4 0.6 0.8 1.0-400-300-200-100
0100200300400
(HS+LS)+HS
(HS+LS+IS)+(HS+LS+IS)
HS+HS
LS+LSLS+(HS+LS)
S HT(
V/K
)x
NaxCoO2 : Spin and orbital degeneracy Co3+ (3d6)/Co4+ (3d5)
J. P. Doumerc JSSC 109, 419 (1994)W. Koshibae et al., Phys. Rev. B 62, 6869 (2000)
)x1
xggln(
ekS
4
3B
x : Co4+ concentration
g4/g3 = 6
Large S in NaxCoO2Origin of the metallicity ?
Models
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Rhombohedral crystalline field Lifting of the t2g levels degeneracy
D. J. Singh, Phys. Rev. B 61, 13397 (2000)
a1g : localized moments / heavy holese ’g : mobile carriers / light holes
FEE
22))ln((
e3k
TS
dE
d
Peak of N(EF)
S = +110V/K at 300Kcalculated for NaCo2O4
T. Yamamoto et al., Phys. Rev. B 65, 184434 (2002)
avec = N(E)<vF(E)2>
Band structure?
Metallic and large S
Models
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M. R. Peterson et al., PRB76, 165118 (2007)
‘Thermoelectric effectsin a strongly correlated model for NaxCoO2’
t-J model : t = hopping and J = spin couplingKubo formalismValid at any T (different from the limit T →)
S = Stransport + SHeikes
Black : Heikes formulaRed : S = Stransport + SHeikes
Models
In a large part of the phase diagram (x, T, t), the Heikes formula gives a good estimate of S
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The Kelvin formulaM. R. Peterson et al., PRB82, 195105 (2010)
t- J model for NaxCoO2 with x ~ 0.7
Heikes formula valid for T > 6 – 8 t(blue curve)
Models
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Models NaxCoO2
First models : crucial role of the CoO2 layers
• Lifting of the t2g orbitals : Seebeck calculated from the Mott’s formula + metallicity
• High T : the Heikes formula, effect of the spin and orbital degeneracies
Beyond the CoO2 layers : the impact of the block layer?
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Electronic correlations + Disorder effectsNaxCoO2
P. Wissgott et al., PRB84, 085129 (2011)
DMFT calculations
Disorder potential induced by Na+ cations
Models
Correlations effect Disorder effect
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Semi-conducteurs : The Heikes formula
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Type p : Pr1-xCaxCrO3 Orthochromites
Perovskite structure
Pr3+1-xCa2+
xCr3+/4+O3 : 3d3/3d2
S. Pal et al., Eur. Phys. J. B 53, 5 (2006)
0 100 200 300 40010-1
100
101
102
103
104
105
106
107
Pr1-xCaxCrO3
x=0.3
(
.cm
)
T(K)
x=0.05
x=0.0
Introduction of holes : Activated behavior with
a decrease of
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Type p : Pr1-xCaxCrO3
0
200
400
600
800
1000
1200
100 150 200 250 300 350T(K)
Pr1-xCaxCrO3
S(V
/K)
x=0.0
x=0.3
x=0.05
OrthochromitesPr3+
1-xCa2+xCr3+/4+O3 : 3d3/3d2
S. Pal et al., Eur. Phys. J. B 53, 5 (2006)
300 350 400 450 500 550 600 650 700100
150
200
250
300
350
400
Pr0.7Ca0.3CrO3
Pr0.95Ca0.05CrO3 Pr0.95Sr0.05CrO3
S(V
/K)
T(K)
Cr4+
Decrease of S induced by doping S constant from 200K to high T
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0.0 0.1 0.2 0.3 0.4 0.5-100
0100200300400500600700800900
1000
x (Ca concentration)
S(
V/K
)
Pr1-xCaxCrO3 Pr1-xSrxCrO3 calculated value taking orbital degeneracy calculated value from Heikes formula
)ln(e
k)x
x1ln(ekS spinorb
BB
Marsh and Parris, Phys. Rev. B 54, 7720 (1996)
K/V9.694133ln
ek B
3d3, S = 3/2
orb=1spin = 4
3d2, S = 1
orb=3spin = 3
Type p : Pr1-xCaxCrO3
Heikes formula withspin and orbital degeneracies
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Type p : Pr1-xCaxCrO3 Power factor
PF ~ 2.10-4 Wm-1K-1
Typical for oxides
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LaCoO3
Heikes formula : possible change of sign
)x
x1ln(e
kS B
x = carrier concentration
-0.4 -0.2 0.0 0.2 0.4-600-500-400-300-200-100
0100200300400500600
S(V
/K)
x
Co4+
(3d5)Co2+
(3d7)Depending on x, S>0 or S<0
Small x |S| very large
Change of sign in LaCoO3
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LaCoO3 : A site substitutionLaCoO3 x~0 : La3+Co3+O3
Sr2+ x>0 : La1-xSrxCo3+Co4+O3
Ce4+ x<0 : La1-xCexCo3+Co2+O3
-0.5 -0.4 -0.3 -0.2 -0.1 0.0 0.1 0.2 0.3 0.4 0.5-600-500-400-300-200-100
0100200300400500600
Co4+Co2+ x
S (
V.K
-1)
A. Maignan et al., EPJB 39, 145 (2004)
50 100 150 200 250 300 350-400
-200
0
200
400
600
800
1000
LaCoO3
Ce0.01
Sr0.02
S (
V.K
-1)
T(K)
Change of sign in LaCoO3
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LaCoO3 : B site substitution
100 150 200 250 300 350
-300
-200
-100
0
100
200
300
400
500
600
700
800
900
1000
LaCo0.995Ti0.005O3
LaCoO3
S (
V/K
)
T(K)
LaCoO3 x~0 : La3+Co3+O3
Ti4+ x<0 : La(Co3+Co2+)1-xTi4+
xO3
Change of sign in LaCoO3
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Formule de Heikes pour S, avec
K. Berggold et al., PRB72, 155116 (2005)
50 100 150 200 250 300 350-400
-200
0
200
400
600
800
1000
LaCoO3
Ce0.01
Sr0.02
S (
V.K
-1)
T(K)-0.5 -0.4 -0.3 -0.2 -0.1 0.0 0.1 0.2 0.3 0.4 0.5
-600-500-400-300-200-100
0100200300400500600
Co4+Co2+ x
S (
V.K
-1)
A. Maignan et al., EPJB 39, 145 (2004)
Co3+ IS
Co4+ LS
)x1
xggln(
ekS
4
3B
Spin only degeneracyg3 = 3 / g4 = 2
Type p : LaCoO3
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Change of sign in LaCoO3
K. Berggold et al., PRB72, 155116 (2005)
LaCoO3
Single crystals measurements
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Type p : LaCoO3 LaCoO3 perovskites
J. Androulakis et al., APL84, 1099 (2004)ZT = 0.18 at 300K
LaCoO3
La0.95Sr0.05CoO3
La1-xSrxCo3+1-xCo4+
xO3
Semi-conducting with 5% hole doping
Eg decreases from 250 meV from LaCoO3to 36meV for La0.95Sr0.05CoO3
ZT=0.18
300K
27m.cm à 300K
Similar as Berggold et al., but much larger S
Oxygen stoechiometry?
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Resistivity of La1-xMxCoO3
0 50 100 150 200 250 300 350 400 45010-2
10-1
100
101
102
103
104
105
106
107
Ti0.01 LaCoO3
Ce0.01
Sr0.02
(o
hm.c
m)
T (K)
Asymmetry between hole and electron doping
Change of sign in LaCoO3
(n type ) > (p type)
Typical of many oxides
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An eg electron Co2+ cannot move in a background of LS Co3+ , requires to flip other spins, wrong spin-states LS Co2+ and IS Co3+ instead of LS
A t2g hole Co4+ can hopin a background of LS Co3+
A. Maignan et al, Phys. Rev. Lett. 93, 026401 (2004)
Change of sign in LaCoO3
Spin blockade mechanism
3d5 / 3d6
3d6 / 3d7
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The 112- family
A. A. Taskin et al., PRB73, 121101 (2006)
The 112 family
Co3+/Co4+ or Co2+/Co3+
Pyramidal and octahedral sitesPossible spin state transitions
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A. A. Taskin et al., PRB73, 121101 (2006)
Calculations of spin/orbital degeneracies taking into account the different sites (octahedral / pyramidal)
Explains the larger values for n type (HS Co2+) compared to p type (LS Co4+)
Quantitative analysis of SThe 112 family
Differences in orbitaldegeneracies
for octahedra / pyramids
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High Temperature properties of manganites
T. T. M. Palstra et al., Phys. Rev. B 56, 5104 (1997)
W. Kobayashi et al., J. Appl. Phys. 95, 6825 (2004)
Spin degeneracy + Orbital degeneracy
S independent on x in a large range of x
)1S21S2ln(
ekS
1
0B
-20V/K -20V/K
-80V/K
S0 = 3/2 (Mn4+)S1 = 2 (Mn3+)
‘Probe’ of Jahn Teller effect
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Semi – conducting oxides
The Heikes formula
→ Possibility to get p and n type oxides
→Spin and/or orbital degeneracies have to be taken into account for a quantitative analysis
→Explains the asymmetry between n and p type
But too large resistivity !
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Degenerate semi-conductors : Best n type oxides
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Type n : ZnO
M. Ohtaki et al., JAP79, 1816 (1996)
Zn1-xAlxO (x = 0 – 0.1)
Broadband model for extrinsic n type semiconductor
Large mobility of the carriers : 3 – 7cm2/Vs
= 40Wm-1K-1 at 300K=5.4 Wm-1K-1 at 1000°C
ZT = 0.3
too high!
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Perovskite Ca1-xSmxMnO3
Partially filled 3d levels
Mn3+ t2g3eg
1, HS JT
V(Mn)=4-x
Type n : CaMnO3
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Type n Perovskite Ca1-xSmxMnO3
A-site doping
T(K)0 50 100 150 200 250 300
10-3
10-2
10-1
( c
m
0.00
0.05
0.075
0.10
0.12 Tp
x
T (K)0 50 100 150 200 250 300
S (
V K
-1)
-400
-300
-200
-100
0
Ca1-xSmxMnO3
0.00
0.05
0.10
x
VMn > 3.5Partially filled 3d levels
Mn3+ t2g3eg
1, HS JTMn4+ t2g
3, HS
Polaronic transport
Type n : CaMnO3
J. Hejtmanek et al., PRB60, 14057 (1999)
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Manganese oxidesn type SrMn1-xMoxO3
0 100 200 300 400 500 600 700 80010-2
10-1
100
101
102
103
x=0
x=0.04x=0.02
(
cm)
T (K)0 100 200 300 400 500 600 700 800-500
-400
-300
-200
-100
0
x=0
x=0.02
x=0.04
S(V
/K)
T (K)
SrMnO3 : Mn4+
Mo6+ Mn3+/Mn4+
Metallic up to high T / S linear in TPower factor increases as T increases : PF = 9.10-4Wm-1K-2 for x=0.02 at 800K
Measurements by J. Hejtmanek (Prague))lnTk/3ekπS BB2 Eσ(E)/(
3d3 t2g3 / 3d4 t2g
3eg1
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Type n : CaMnO3 Ca0.9M0.1MnO3
M. Ohtaki et al., JSSC120, 105 (1995)
ZT ~ 0.1 à 900°C
S ~ T
Carrier concentration1019 -1021 cm-3
J. L. Cohn et al., PRB72, 024422 (2006)
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n type : SrTiO3
SrTiO3 = non magnetic insulatorLa3+ : doping of Ti3+ in a matrix of Ti4+
T. Okuda et al., PRB63, 113104 (2001)
Sr1-xLaxTiO3
PF = 28 -36 WK-2m-1
But electrical conductivity too large!!
~ n(Constant mobility) Boltzmann model for a parabolic band
Degenerate semi-conductor
ZT = 0.22 for Sr0.9Dy0.1TiO3at 573K
H. Muta et al., J. Alloys and Comp.350, 292 (2003)
n ~1020 – 1021 cm-3
3d0 / 3d1
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smaller than for p type oxidesLess sensitive to correlation effects
n type : SrTiO3 Sr1-xLaxTiO3
T. Okuda et al., PRB63, 113104 (2001)
Carrier concentration1019 -1021 cm-3
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Type p : delafossites CuCr1-xMgxO2 delafossitesCrO2 layers : edge shared octahedra
T. Okuda et al., PRB72, 144403 (2005), Y. Ono et al., ICT 2006
ZT = 0.04 at 950K
CuRh0.9Mg0.1O2 : ZT = 0.15 à 1000KH. Kuriyama et al., ICT2006
Possibility to get p type oxides
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10 20 30 40 50 60 70 80 90
0.0 0.1 0.2 0.30.00
0.05
0.10
0.15
0.20
In2Ge2O7
In2O3
I (a.
u.)
2
In2G
e 2O7 f
ract
ion
Nominal Ge fraction
No substitution occursor
Small Ge solubility limit
SampleIn1.9Ge0.1O3
RBragg= 2.98, Chi2=1.28
XRDIn2-xGexO3
C. Marcel et al., Active and Passive Elec. Comp., 1997, Vol. 19, pp. 217-223
D. Bérardan et al., Solid Stat. Comm. 146 (2008) 97.
Doping or microstructure effect??
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SampleIn1.8Ge0.2O3
EDS analyses: Ge is not detectable in the grains
No grain size modification
In2Ge2O7
MicrostructureIn2-xGexO3
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In2O3 doped with Ge
D. Bérardan et al., Solid Stat. Comm. 2008
Type n : In2O3
0,00 0,05 0,10 0,15 0,200,0
0,1
0,2
0,3
0,4
0,5
1273 K 873 K 573 K 298 K
ZTGe fraction (x)
300 400 500 600 700 800 900 1000 1100-240
-220
-200
-180
-160
-140
-120
-100
-80
-60
-40
S (
V.K-1
)
T (K)
x=0 x=0.002 x=0.004 x=0.006 x=0.01 x=0.015 x=0.02 x=0.04 x=0.06 x=0.1 x=0.2 x=0.3
300 400 500 600 700 800 900 1000 1100
1
10
(m
.c
m)
T (K)
x=0 x=0.002 x=0.004 x=0.006 x=0.01 x=0.015 x=0.02 x=0.04 x=0.06 x=0.1 x=0.2 x=0.3
0,00 0,05 0,10 0,15 0,201
2
3
4
5
6
7
8
9
10
(W
/m.K
)
Ge fraction (x)
300K 573K 873K 1273K
In2-xGexO3
ZT = 0.4 à 1273K
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Doped CaMnO3 : New preparation techniques
Soft chemistry techniques
L. Bocher et al., Inorg. Chem. 47, 8077 (2008)
Reduction of Possible size effect?
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Degenerate semi - conductors
• Classical behavior which can be described by the Boltzmann modelVery small enhancement of the effective mass
• Mostly n type (p tye in delafossites)
• Problem : too large thermal conductivityMicrostructure modification is necessary to enhance ZT
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NaxCoO2 and related metallic compounds(p type)
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Cobalt bronzes family ofNaxCoO2
C. Fouassier et al., JSSC6, 532 (1973)
J. Molenda, C. Delmas, P. Dordor, A. Stoklosa, Solid Stat. Ionics 12, 473 (1989)
Na0.7CoO2-
T
S
T
NaxCoO2Misfits
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Metallicity (crystals) ~ 0.2 m cmLarge S S ~ +80 V/KSmall (polycrystals) Wm
(crystals) ~ 5Wm-1K-1
Na0.7CoO2‘ Phonon Glass / Electron crystal ’
I. Terasaki et al., Phys. Rev. B 56, R12685 (1997)
Na0.7CoO2P= 50 10-4 WK-2m-1
Bi2Te3P= 40 10-4 WK-2m-1
At 300K
Power factor P=S2/ at 300K
Co3+ (3d6) / Co4+ (3d5)
NaxCoO2 : Na+xCo3+
xCo4+1-xO2 Measurements on polycrystals
Introduction
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Heikes formula : doping influence?Band structure influence : peculiarity of CoO2 layers ?
Role of separating block layers?
b2
a NaxCoO2KxCoO2, …
Misfits
NaxCoO2Misfits Lamellar oxides with CoO2 layers
Triple AO layer (NaCl-type)
Misfit family : 2, 3 or 4 separating layers
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M. Blangero et al., Inorg. Chem. 44, 9299 (2005)
KxCoO2
Modification of the block layersNaxCoO2Misfits
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0 50 100 150 200 250 30001234567
'Tl0.4SrCoO3+'
'Ca3Co4O9'
(10
-2
cm)
T(K)
Misfits
Modification of the block layersNaxCoO2Misfits
0 50 100 150 200 250 3000
20
40
60
80
100
120
140
'Tl0.4
SrCoO3+
'
'Ca3Co
4O
9'
S(V
/K)
T(K)
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0 50 100 150 200 250 300
0
20
40
60
80
100
120
140
160
As-prep.
Po2
S(V
/K)
T(K)
Unique behavior of CdI2 type layers: Comparison with other oxides
Perovskite Sr2/3Y1/3CoO8/3+
Corner shared octahedraedge shared octahedra
A. Maignan et al., JSSC178, 868 (2005)
Metallicity
Seebeck 0
NaxCoO2Misfits
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Oxygen content influence
Ca3Co4O9+Co4+
M. Karppinen et al., Chem. Mater. 16, 2790 (2004)
NaxCoO2Misfits
Misfits : S the largest for the smallest ‘Co4+’ content
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Doping effect in the misfit family
21 /4v
bbCo
Ca2CoO3NaCl-like
CoO2CdI2-like
Ca3Co4O9 Electronic neutrality :[Ca2CoO3±]RS[CoO2]b1/b2
2+ 2-3+ Co 2-
>0
Modification of vCo via and b1/b2
Link between vCo and S?
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0 100 200 300 400
100
101
102
BSCO
BPSCO
(m
cm
)
T(K)
BiSrPbCoO single crystals : modification of
[Bi1.5Pb0.5Sr2O4-δ][CoO2]1.86[Bi1.74Sr2O4][CoO2]1.82
Metallic behavior down to 5K with = AT2
Characteristic of electronic correlations
Substitution of Bi3+ by Pb2+ : decrease of Increase of vCo
21 /4v
bbCo
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0 50 100 150 200 250 3000
20
40
60
80
100
120
BSCO
BPSCO
S(V
/K)
T(K)0 100 200 300 400
100
101
102
BSCO
BPSCO
(m
cm
)
T(K)
Increase of ‘Co4+’ associated to a decrease of S
Generalized Heikes formula : increase of vCo
3.59 for BSCO and 3.65 for BPSCO
NaxCoO2Misfits BiSrPbCoO single crystals : modification of
)x1
xggln(
ekS
4
3B
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BiSrPbCoO single crystals : modification of
0 50 100 150 200 250 3000,000
0,005
0,010
0,015
BPSCO
BSCO
RH
(cm
3 /C)
T(K)
At 100K1.06 × 1021 cm-3 for BSCO 1.73 × 1021 cm-3 for BPSCO
W. Kobayashi et al., JPCM21, 235404 (2009)
t- J model : Linear T dependence of RHt ~10 – 40K
Justifies the Heikes formulaB. Kumar et al., PRB68, 104508 (2003)
Y. Wang et al., cond-mat/0305455G. Leon et al. , PRB78, 085105 (2008)
Increase of vCo3.113.18
NaxCoO2Misfits
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W. Kobayashi et al.
0 50 100 150 200 250 3000
2
4
6
8
10
12
14
BiBaCoO
BiSrCoO
BiCaCoO
(m
.cm
)
T(K)0 50 100 150 200 250 300
0
20
40
60
80
100
120
140
160
BiBaCoO
BiCaCoO
BiSrCoO
S (
V/K)
T(K)
0 50 100 150 200 250 3000.000
0.005
0.010
0.015
0.020
0.025
0.030
BiBaCoO
BiSrCoO
BiCaCoO
RH(c
m3 /C
)
T(K)
Influence of b1/b2
b1/b2
21Co b/b
4v
If b1/b2 , concentration of Co4+
S at 300K depends on Co4+
modified through b1/b2
NaxCoO2Misfits
1.65 1.70 1.75 1.80 1.85 1.90 1.95 2.0080
90
100
110
120
130
140
150
BiBa
BiSr
BiPbCa
BiCa
S 300K
(V/
K)
b1/b2
Carrier concentration ~ 1022 cm-3, larger than for conventional thermoelectrics
b1 : NaCl layers / b2 : CoO2 layers
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Heikes formula
)xx-1
ggln(
ekS
3
4B
Co valency in BiCaCoO/ BiSrCoO / BiBaCoO?
0,0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1,0-300
-200
-100
0
100
200
300
400
500
600
Spin degeneracyCo3+ S = 1/2 + Co4+ S=0 : =1/2
Heikes = 0
Spin and orbital degeneracyCo3+ LS + Co4+ LS : =1/6
S Hig
hT(
V/K)
x
3.05 -3.153.5 -3.7 for g4 / g3 = 6Hall effectHeikes (S at 300K)
NaxCoO2Misfits
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Carrier concentration10
8
6
4
2
0
10
8
6
4
2
0
single hole-like fermi surface (a1g character)
21Co b/b
4v
kF=0.57±0.05 Å-1 for BiBaCoO
similar to kF of NaxCoO2 (x=0.7)
Collaboration with V. Brouet et al., LPS Orsay
Co3.3+ for BiBaCoO
Reliable data for vCo are obtained for BiBaCoO
Co3.2+ for BiSrCoOCo3.1+ for BiCaCoO
(=const)
V. Brouet et al., PRB76, 100403 (2007)
ARPES
NaxCoO2Misfits
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Heikes formula
)x1
xggln(
ekS
4
3B
g3 / g4 = 1/2 instead of 1/6 Confirms the results in BiCaCoO : vCo = 3.24
M. Pollet et al., JAP101, 083708 (2007)
0,0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1,0-300
-200
-100
0
100
200
300
400
500
600
Spin degeneracyCo3+ S = 1/2 + Co4+ S=0 : =1/2
Heikes = 0
Spin and orbital degeneracyCo3+ LS + Co4+ LS : =1/6
S Hig
hT(
V/K)
x
NaxCoO2Misfits
Co valency in BiCaCoO/ BiSrCoO / BiBaCoO
3.24M. Pollet et al.,
JAP101, 083708 (2007)
3.1 -3.3J. Bobroff et al., PRB76, 100407
(2007)
3.3V. Brouet et al.,PRB76, 100403
(2007)
3.05 -3.15W. Kobayashi et al.
3.33P. Limelette et al., PRL97, 046601
(2006)
3.5 -3.7
SusceptibilitéBiCaCoO
RMNARPESBiBaCoO
Effet HallSeebeck avec S(H)g3/g4 = 1BiCaCoO
Heikesg3/g4 = 1/6S à 300K
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Orbital filling in NaxCoO2 and misfit cobaltiteswith edge-shared CoO6
Ligand field splitting :trigonal distortion
MB Lepetit
LS Co3+/Co4+ mixed-valency
metallicity
a1g
e’g
= 1/61 for Co3+ but 2 instead of 6 for Co4 +
= 1/2
NaxCoO2Misfits
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NaxCoO2Misfits Influence of electronic correlations
P. Limelette, PRB71, 233108 (2005)
csteeNTSq Av
For T→0
P. Limelette, PRL97, 046601 (2006)
S ~ T
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Low T : Spin entropy
BiCaCoO : excess of S at low TA. Maignan et al., JPCM 15, 2711 (2003)
Observed also in NaxCoO2[Wang et al. Nature 423, 425 (2003)]
NaxCoO2Misfits
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Scaling MR et MTEPLien avec la susceptibilité
Spin entropy at low TMisfit BiCaCoO
Na0.7CoO2
A. Maignan et al., JPCM15, 2711 (2003)
Y. Wang et al., Nature423, 425 (2003)
Scaling law for S(H) : paramagnetic spins S=1/2Brillouin function
P. Limelette et al., PRL97, 046601 (2006)
Decrease of S under field at low TDue to the alignement of paramagnetic spins
Peak of susceptibility
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Misfits
CoO2 (type CdI2)
NaCl-like triple layer (RS)
Co3+ (3d6) / Co4+ (3d5)Low spin : t2g orbitals+ triangular network
0 50 100 150 200 250 300100
101
102
103
104
BiBaCoOBiSrCoO
BiCaCoO
(m
.cm
)
T(K)
0 50 100 150 200 250 3000
20
40
60
80
100
120
140
160
BiBaCoO
BiCaCoO
BiSrCoO
S (
V/K)
T(K)
For T > 100K : metallicity + large S
• High T : Seebeck depends on Co4+
Heikes formula with spin / orbital degeneracye)
• Low T : electronic correlations : S ~ T+ spin entropy depending on doping
• High T limit : small t from Hall effect. Justifies the Heikesformula
S. Hébert et al., PRB64, 172101 (2001), P. Limelette et al., PRL97, 046601 (2006), W. Kobayashi et al., JPCM21, 235404 (2009)
Misfit oxidesNaxCoO2Misfits
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0 50 100 150 200 250 3000
20406080
100120140160
S(V
/K)
T(K)
Thermoelectric power of misfits
Spin entropy (depending on doping)Electronic correlations : S ~ T
High T Seebeck, depends on Co4+
(Heikes formula with = 1/2)
BiCaCoO
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Power factor
0 100 200 3000
1
2
3
4
Temperature (K)
Pow
er F
acto
r (W
/cm
K2 )
BiSrCoO
BiPbSrCoO
BiBaCoO
BiCaCoO
enhancement for BiBaCoO and BiPbSrCoO
P is almost independent of carrier concentration
In conventional semiconducting thermoelectric material such as Bi2Te3, n is an important parameter to tune the properties.
How to modify the electronic properties?Influence of the block layer?
2.10-4 Wm-1K-2 at 300K
NaxCoO2Misfits
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Role of the block layer?
• Role of Na+ : Curie-Weiss behavior obtained by introducing theelectrostatic potential of Na+ (Co3+ S = 0 / Co4+ S = 1/2)C. Marianetti et al., PRL98, 176405 (2007)
•Kagomé lattice in NaxCoO2 with x = 2/3 : strong electronic correlationsF. Lechermann et al., PRL107, 236404 (2011)
Curie-Weiss
NaxCoO2Misfits
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NaxCoO2Misfits High T measurements in Ca3Co4O9
Increase of S at high T
Measurements in air?
M. Shikano et al., APL82, 1851 (2003)
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NaxCoO2Misfits Thermal conductivity
Measurements of single crystals (Harman method)
A. Satake et al., JAP96, 931 (2004)
smaller in misfits
Influence of incommensurability?
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• Charge transfer between the layers : S300K mostly depends on the ratio Co3+/Co4+
• Low T : electronic correlations influence (S ~ T) + S(H) term
• Small
Power factor is constant : modification of the block layers? Influence on thermal conductivity?
NaxCoO2Misfits Conclusion
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Nanostructuration
![Page 94: Oxides for thermoelectricity - UCSB MRSECseshadri/2012-SummerSchool-Talks/UCSB-2012-Hebert.pdf · influence of electronic correlations K. Behnia et al. JPCM 16, 5187 (2004) Free electron](https://reader033.vdocument.in/reader033/viewer/2022042105/5e834b03f53adc6f8d490149/html5/thumbnails/94.jpg)
2DEG SrTiO3
Nanostructuration :Increase of S
2D electron gas in SrTiO3H. Ohta et al., Nat. Mater. 6, 129 (2007)
‘ZT’ = 2.4!
of SrTiO3 single crystals
SrTi1-xNbxO3
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NaxCoO2 nanowires
Sol-gel electrospinning
F. Ma et al., J. Phys. Chem. C 114, 22038 (2010)
~ .m?Resistivityoverestimated by 3 orders ofmagnitude by themeasurementtechnique?
Same technique as for Ca3Co4O9
Lin et al., J. Phys. Chem. C 114, 10061
(2010)
Nanostructuration
![Page 96: Oxides for thermoelectricity - UCSB MRSECseshadri/2012-SummerSchool-Talks/UCSB-2012-Hebert.pdf · influence of electronic correlations K. Behnia et al. JPCM 16, 5187 (2004) Free electron](https://reader033.vdocument.in/reader033/viewer/2022042105/5e834b03f53adc6f8d490149/html5/thumbnails/96.jpg)
J. Ravichandran et al., PRB85, 085112 (2011)
Strong correlations + Size effects
Correlation effect :
Behavior different from the oneclassical observed through thesurface diffusion mechanism(Fuchs – Sondheimer model)
Thin films of BiSrCoO misfits
Decoupling of resistivity and Seebeck?
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Oxide modules
![Page 98: Oxides for thermoelectricity - UCSB MRSECseshadri/2012-SummerSchool-Talks/UCSB-2012-Hebert.pdf · influence of electronic correlations K. Behnia et al. JPCM 16, 5187 (2004) Free electron](https://reader033.vdocument.in/reader033/viewer/2022042105/5e834b03f53adc6f8d490149/html5/thumbnails/98.jpg)
Modules Oxide prototypes
W. Shin et al., JJAP39, 1254 (2000)
n : Ba0.4Sr0.6PbO3 Z = 2.10-4 K-1 at 673K (ZT = 0.13)p : Li0.025Ni0.975O Z = 0.75 10-4 K-1 at 1273K (ZT = 0.095)
One leg : 4.8 ×4.9 × 17.5 mm3
One pair : 7.91mWTH = 987KT = 552K
1st prototype in 2000
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Oxide prototypes
I. Matsubara et al., APL 78, 3627 (2001)
n : Ca0.92La0.08MnO3 / p : Ca2.75Gd0.25Co4O98 pairs 3 × 5 × 30 mm3
Th = 1046K , T = 390K, P=63.5mW
Modules
TC = 370°CTH = 650°C
Stability
![Page 100: Oxides for thermoelectricity - UCSB MRSECseshadri/2012-SummerSchool-Talks/UCSB-2012-Hebert.pdf · influence of electronic correlations K. Behnia et al. JPCM 16, 5187 (2004) Free electron](https://reader033.vdocument.in/reader033/viewer/2022042105/5e834b03f53adc6f8d490149/html5/thumbnails/100.jpg)
Modules La0.9Bi0.1NiO3 / Ca2.7Bi0.3Co4O9
R. Funahashi et al., APL 85, 1036 (2004)R. Funahashi et al., JAP99, 066117 (2006)
n : La0.9Bi0.1NiO3 / p : Ca2.7Bi0.3Co4O91 jonction : TH = 1073K, T = 500K, P = 94mW
140 pairesTH = 1072K, T = 551K
For mobile phoneTH = 1072K!
![Page 101: Oxides for thermoelectricity - UCSB MRSECseshadri/2012-SummerSchool-Talks/UCSB-2012-Hebert.pdf · influence of electronic correlations K. Behnia et al. JPCM 16, 5187 (2004) Free electron](https://reader033.vdocument.in/reader033/viewer/2022042105/5e834b03f53adc6f8d490149/html5/thumbnails/101.jpg)
Modules
0.150.0162NCa0.95Sm0.05MnO3/ Ca0.95Sm0.05MnO3
Present work
0.570.0312PNCa3Co4O9 / Ca0.95Sm0.05MnO3Sudhakar et al.
0.820.0898PN(Gd) Ca3Co4O9 / (La) CaMnO3Matsubara et al.
0.30.0342PN(Li) NiO / (Ba, Sr) PbO3Shin et al.
0.150.031PNCa2.7Bi0.3Co4O9 / La0.9Bi0.1NiO3Funahashi et al.
MFPower (W)Nb CoupleTypeMaterialsName
Comparison of modules
Manufacturing factorMF = Rideal / Rint,
S. Lemonnier, C. Goupil et al.
Important to optimize the contacts quality!
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Type n : SrTiO3 dopé au La450mW/cm2 pour T = 360K
Modules and prototypesDevices
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Stability problems
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Thermal stability
Oxides : can be synthesized in air or controlled atmosphere at 800°C – 1500°C
Misfits : 800 - 1000 °C in air, or controlled atmosphereLa1-xSrxCo3+
1-xCo4+xO3 : 1250°C
Pr3+1-xCa2+
xCr3+/4+O3 : 1500°C in O2CuCr1-xMgxO2 : 1200°C in airCa0.9M0.1MnO3 : 1300°C in air
Zn1-xAlxO : 1400°C in airSr1-xLaxTiO3: 1400°CIn2O3 : 1300°C in air
Oxygen stoechiometry?
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Perovskites
B. Dabrowski et al., JSSC170, 154 (2003)
Type n : manganese oxides
CaMnO3Stable jusqu’à ~ 700 -800°C
sous O2
Thermal stability
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Misfits
Oxygen stoechiometry?
Y. Morita et al., JSSC177, 3149 (2004)
N2 annealing
Thermal stability
Thermogravimetric+ titration analysis
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Synthesis and measurements conditions : ZnO
D. Bérardan et al., GDR Thermoélectricité, Grenoble, juin 2010
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D. Bérardan et al., GDR Thermoélectricité, Grenoble, juin 2010
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Seebeck coefficient : Major role of the spin and orbital term
Importance of electronic correlations
Conclusion
• n type oxides : degenerate semi-conductorsSeebeck described in a first approach by Mott’s formula
• p type oxides
)xx-1ln(
ekS B
ZT (n type) < ZT (p type)Thermal conductivity : coming from the lattice
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How to enhance ZT??
Investigation of thermal conductivity
Nanostructuration and electronic correlations?
Low dimensional structures
Microstructures
Anionic subsitutions (oxyselenides)
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Collaborators
Laboratoire CRISMATWataru Kobayashi (Tsukuba), Hidefumi Takahashi (Nagoya),
Antoine Maignan, Christine Martin, Denis Pelloquin, Olivier Perez
Patrice Limelette, LEMA, ToursJulien Bobroff, Véronique Brouet, LPS Orsay
This work is supported by FP7 European Initial Training Network SOPRANO (GA-2008-214040)