Resonant X-ray Diffraction (REXD)
Transcript of Resonant X-ray Diffraction (REXD)
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Resonant X-ray Diffraction (REXD)
where Diffraction meets Spectroscopy
Yezhou Shi
Department of Materials Science and Engineering, Stanford University
7th SSRL School on Synchrotron X-ray Scattering Techniques
June 3, 2014
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outline
1. motivation: why do we/you care?
2. technique: how does this work?
3. design experiments: what to consider?
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site-specific chemical information
important to understanding properties o materials property depends directly on site occupancies
o complex oxides: multiple sites, multiple cations & anions
perovskite: ABO3 spinel: A2BO4
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o elemental/chemical selectivity
• different elements and/or oxidation states
o site selectivity:
• site A vs. site B
• substitution vs. interstitial
requirements of an ideal technique
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o relatively fast to perform and can refine both elemental and site information
o refine a variety of structural parameters (occupancy, strain, displacement, etc…)
o limitations
• have to deal with all phases/structures in the sample
• elements with similar z chemical selectivity lost
• Alternative: neutron scattering best with large mass
Large-range diffraction +
Rietveld refinement
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outline
1. motivation: why do we/you care?
2. technique: how does this work?
3. design considerations
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principles of resonant X-ray diffraction
2)( hklFEI )(2),( lzkyhxi
i
iihkl eEQfxF
1 2( ) ( ) ( )of f Q f E if E
Bragg (h,k,l)
site selectivity element
selectivity
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model fitting to extract site occupancies
2)( hklFEI )(2),( lzkyhxi
i
iihkl eEQfxF
real part: f1
imag. Part: f2 Combine the best of two worlds:
simultaneously chemical and structural info.
occupancy
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data collection: diffraction scans at
various incident X-ray energies
ϕ incident x-ray
(tunable energy) diffracted x-ray
sample
Co K edge
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The other half of the story:
experimentally determined f1 & f2
KKT
imaginary: f2 real part: f1
measured spectra
near the abs. edge Absorption
coefficients
Stitched to
theoretical values
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outline
1. motivation: why do we/you care?
2. technique: how does this work?
3. design considerations
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designing your experiments:
practical considerations
o is resonant diffraction the tool? • Sr vs Ti in STO • Fe vs Ti in Fe doped STO • 0.1% doped Fe?
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designing your experiments:
practical considerations (cont’d)
o ideally, single phase with known composition
o can you identify one or a set of Bragg peaks to extract site-
specific information?
o trade off between absorption and diffracted intensity
• textured thin films: easiest to work with
• powder/nanocrystals: fine
• polycrystalline film: diffraction too weak
Material/Mass More Less
Absorption More (bad) Less (good)
Diffraction Singal Strong (good) Weak (bad)
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designing your experiments:
drawbacks and limitations
o insensitive to low Z elements or O vacancy (generally true to
hard X-ray based techniques)
o relatively long data acquisition time (30 to 50 energies per
element 6 to15 hrs) – plan your experiments carefully
o model fitting is required to understand the data (no
commercial software to do this)
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designing your experiments:
resources at SSRL
o in-situ experiments possible (elevated T, gas environments…)
o “sweet spot” elements: Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge
• K edges readily accessible with large photon flux
o who to talk to?
• Kevin Stone, Badri Shyam and me
beamline # motors sample form comments
2-1 Two-circle Powder / nanocrystals Less crowded
10-2 Four-circle Thin film/single crystal Sufficient for most purposes
7-2 Six-circle Thin film/single crystal Strange geometries available
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BONUS (Example):
Mn occupancies in Cr2MnO4 spinels
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spinel structure and anti-site defects
• two structurally inequivalent sites: tetrahedral vs. octahedral
• intrinsic anti-site defects created by cross-substitution
4
2
2
3 ][)( OBA TdOh
4121 ][)( OBABA Td
yy
Oh
xx
acceptor
states
donor
states
2
OhB 3
TdA(222)
peak
(422)
peak
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spinel oxide thin film fabrication
• pulsed laser deposition of
Cr2MnO4 on top of SrTiO3
single crystal substrate
• two different compositions
from two PLD targets
•XRD confirm the film is
biaxially textured
ϕ
SrTiO3 substrate (a = 3.9 Å)
Cr2MnO4 (a = 8.4 Å)
2θ/ω scan: Out-of-plane
ϕ scan: in-plane
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Cr2MnO4 spinel: spectroscopy offers
a qualitative yet incomplete picture
Shi, Y. et al, Chem. Mater., 2014, 26 (5), pp 1867–1873
Cr edge: Cr (III) only Mn edge: (II) + (III)
1 2 1 4( ) [ ]Oh Td
x x y yMn Cr Mn Cr O
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site-dependent chemical shifts near Mn edge
• chemical shift related to Mn oxidation states
• a larger shift is observed for MnOh than the MnTd in both samples
screen and actually point where the dips
Cr2MnO4
theoretical edge: 6539 eV
Td site dip: 6546 eV Oh site dip: 6549 eV
Cr1.5Mn1.5O4
Td Td
Oh Oh
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fitted site occupancies for Cr2MnO4
Shi, Y. et al, Chem. Mater., 2014, 26 (5), pp 1867–1873
• how do we know Mn are indeed (II) on Td sites
and (III) on Oh sites?
compare dip position and fine features
• Td site data (422 reflections) are very similar to
the simulated REXD of Fe2MnO4 with Mn(II)
• Oh site data (222 reflections) are very similar to
the simulated REXD of Mn2O3 with Mn(III)
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fitted site occupancies for Cr2MnO4
• compare Mn edge data to references: Td site is Mn(II) whereas Oh site
is Mn(III)
• four data sets are fitted independently to give site occupancies –
occupancies sum up to unity for both sites
Shi, Y. et al, Chem. Mater., 2014, 26 (5), pp 1867–1873
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complimentary information from
absorption & emission spectroscopies N
orm
aliz
ed a
bso
rban
ce XES @ SSRL 6-2
No
rmal
ized
inte
nsi
ty
XAS @ SSRL 4-1
Film
Composition
(XRF)
Site Occupancies
(REXD)
Calculated Mn
Ox. States
(REXD)
Averaged Mn
Ox. States
(XANES)
Averaged Mn
Ox. States
(XES)
Cr1.83Mn1.17O4 Cr1.7Mn1.3O4 2.23 ± 0.02 2.13 ± 0.12 2.25 ± 0.04
Cr1.33Mn1.67O4 Cr1.4Mn1.6O4 2.38 ± 0.03 2.26 ± 0.11 2.33 ± 0.04
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Thank you for your attention.