High-Field Solid-State NMR: The Tools and Their Application in … · 2010. 10. 3. · High-Field...
Transcript of High-Field Solid-State NMR: The Tools and Their Application in … · 2010. 10. 3. · High-Field...
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High-Field Solid-State NMR:The Tools and Their Application
in Materials Research
High-Field Solid-State NMR:The Tools and Their Application
in Materials Research
Arno KentgensDepartment of Physical Chemistry / solid-state NMR,Institute for Molecules and Materials,Radboud University Nijmegen, The Netherlands.
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OutlineOutline�Basic NMR Introduction
�Solid-State NMR
�NMR tools for spin 1/2�Case Study: melaminephosphate flame retardants�NMR tools for quadrupolar nuclei
�NMR tools for the future
�NMR above 30 T (1.27 GHz)�Microcoil NMR�Polarization Enhancement Techniques�Mechanical Detection of Magnetic Resonance
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Nijmegen Science Faculty &Goudsmit Pavilion for NMR Research
Nijmegen Science Faculty &Goudsmit Pavilion for NMR Research
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The Concept of SpinThe Concept of Spin
Goudsmit en Uhlenbeck 1925: Electrons have anintrinsic magnetic moment caused by the rotation of
the electron
Goudsmit Pavilion for NMR Research
Goudsmit -Pauli – Stern 1926: nuclear
spin
Zeeman effect
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Nuclear Spin HamiltonianNuclear Spin Hamiltonian� Quantum state of the entire sample is fully described by a wave
function |ψfull>
� Effects of rapidly moving electrons is blurred out, their “average”effect is contained in the spin Hamiltonian:
)(ˆ)( tHitdt
dfullfullfull ψψ −=
)(ˆ)( tHitdt
dspinspinspin ψψ −= Magnetic
Field
ElectricField
MagneticMoment
ElectricCharge
++
+
+
++
Study Malcolm H. LevittSpin Dynamics, Wiley, 2001
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Nuclear Zeeman InteractionNuclear Zeeman Interaction
�Spin interacts with external magnetic field:
0,// ˆˆˆˆˆ 0 BIHBIBH zjj
jZeeman
zBjjj
jZeeman γγµ −= →−=⋅−=
rr
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Transverse RF fieldTransverse RF field
xy
z
Coil
B0
B (t)RF
time
B RF
+
x
xx
y
y
y
z
z z
Oscillating
Rotating
1
,0,01
2
1frequencynutation
}ˆ)sin(ˆ){cos(2
1ˆ
B
ItItBH
jnut
yjpxjpjj
RF
γω
φωφωγ
=
+++=
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Precession in the Magnetic FieldPrecession in the Magnetic Field
Larmorprecessionfrequency
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The basic NMR experimentas viewed from the rotating frame
The basic NMR experimentas viewed from the rotating frame
� The magnetization is tipped over by a rf-pulse. The precession of the magnetization in the field induces a voltage in the receiver coil.
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From Free Induction Decayto Spectrum
From Free Induction Decayto Spectrum
Fourier Transform
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Chemical ShiftChemical Shift
HFML Nijmegen
diamagnetism
zjzzjjj
CS
zzjzyjzxj
yzjyyjyxj
xzjxyjxxj
inducedj
inducedjlocj
IBH
B
B
BBB
,,0
0,,,
,,,
,,,
,
,0,
ˆ)(ˆ :ionapproximatsecular
0
0
θδγ
δδδδδδδδδ
−≅
⋅
=
+=
r
rr
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Ethanol: CH3CH2OHEthanol: CH3CH2OHPackard, Stanford 1951
Purcell: “Indeed certain branches of this work are now being pursued in chemical laboratories.”
)(3
1
ˆˆ
:shift chemical averaged
motionally liquids isotropicIn
,,,,
,,0,
zzjyyjxxjisoj
zjisojjj IBH
isoCS
δδδδ
δγ
++=
−≅
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Anisotropic InteractionsAnisotropic InteractionsLiquid: rotational and translational motions
Single crystal
B0
ω
PowderSpectrum
IndividualPeaks
δ11
δ33
δ22
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What Information Can NMR GiveWhat Information Can NMR Give
Site Identification
•Chemical Shift�Identification of structural building blocks (1H,13C).�Coordination of 27Al, 69,71Ga, 29Si etc).�Hydrogen bonding (1H,15N,17O)�Majority of periodic table is accessible
•Knight shifts, Fermi-contact shifts etc (Lecture Berthier).�Li-ions in paramagnetic battery materials
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Anisotropic 13C interactionsAnisotropic 13C interactions
alignment
identificationMolecular motions
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Site IdentificationSite Identification
δcs Tetrahedral Al-O-Si
in aluminosilicates
27Al NMR of oxides
4-fold coordinated Al: 80 - 40 ppm
5-fold coordinated Al: 40 - 20 ppm
6-fold coordinated Al: 20 - -10 ppm
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Anisotropic InteractionsAnisotropic Interactions
� Broad lines
☺ Structural information
☺ study dynamics
☺ Manipulation in ordinary and spin space
� use adequate tools
Na3PO4
Na4P2O7
(NaPO3 )n
31P powder spectra
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Tool: Magic-Angle SpinningTool: Magic-Angle SpinningAveraging of anisotropic interactions in
ordinary coordinate space. 12000 Hz
870 Hz
static
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Direct dipole-dipole interactionsDirect dipole-dipole interactions
jk j k
( )
( )( )( )( )kzjzjkjkjk
jkDD
kjkzjzjkjkjkjk
DD
jk
kjjkkjkjjkjk
DD
IIbH
IIIIbH
e
IIeIeIbH
ˆˆ21)(cos3)(ˆ :earheteronucl
ˆˆˆˆ31)(cos3)(ˆ :rhomonuclea
:ionapproximatsecular
k and jspin connectingr unit vecto theis
ˆˆ)ˆ)(ˆ(3ˆ
2
2
−=
⋅−−=
⋅−⋅⋅=
θθ
θθ
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Anisotropic Dipolar InteractionAnisotropic Dipolar Interaction
r12
Pake doublet
For abundant spins MAS is only effective if spinning speed significantly exceeds the line width
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What Information Can NMR GiveWhat Information Can NMR Give
Intersite correlations•Dipolar Interactions (through space)
�Spatial proximity of nuclei (~1/r3)�Homonuclear�Heteronuclear
•J-couplings (mediated through chemical bonds)�Existence of chemical bonds.
•Hyperfine interactions (coupling to electron spin > Lecture Berthier).
r12
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Tool: Radio Frequency IrradiationTool: Radio Frequency Irradiation
Manipulation of interactions in spin space.
� Heteronuclear decoupling of nuclei by CW-irradiation with resonant RF waves. Pulsed alternatives TPPI, XiXetc.
� Homonuclear decoupling by CW irradiation at the magic angle (Lee-Goldburg decoupling). Pulsedalternatives: WAHUHA, MREV-8, FSLG, Dumbo etc.
CW-decoupling<Iz>=0
LG-decoupling<3Ij,zIk,z-IjIk>=0
<Iz>=1/√3 Iz
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Combining ToolsCombining Tools
�Combined Rotational and Multiple Pulse Decoupling
�Recoupling of dipolar interactions using radio-frequency sequences synchronized with sample spinning and matched rf-field strength.
�Transfer of coherence of coupled nuclei
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1H Spectroscopy1H Spectroscopy
A. Lesage, L. Duma, D. Sakellariou, and L. Emsley, J. Am. Chem. Soc. 123, 5747 (2001)
static
MAS
30 kHz MAS
RF
FSLG12.5 kHz MAS
Alanine
CH2
CHNH3
+
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Combining ToolsCombining ToolsNatural RubberAdamantane
13C Single Pulse Excitation
+ 1H CW Decoupling
+ Magic Angle Spinning
+ MAS + 1H LG decoupling
+ MAS + 1H CW decoupling
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Two-dimensional NMRTwo-dimensional NMR(π/2)
φrec
φdig
,φ2
(π/2)φ1
1t 2t
1t
1t
2t
2t
Fourier Transformt2 and t1
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Case Study: Environment-Friendly Condensed Phase Flame Retardants
Case Study: Environment-Friendly Condensed Phase Flame Retardants
Melamine
MPhosphoric Acid
P
+Melamine Phosphates:
MP(MP)2 (Pyrophosphate)
M Polyphosphate
Polymerization
Conversion ~200 °°°°C - 260°°°°CAbove 260 °°°°C decomposition
Crystal structures unknownPolymerization process unknown
FR Mechanism unknown
A. Brinkmann, E.R.H van Eck & A.P.M. KentgensMagnetic Resonance in Chemistry, 2007 submitted
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Site ID with added anisotropic information
Site ID with added anisotropic information
MP
(MP)2
MPpoly
PO4
P2O7
(PO3 )n
σ11 = 46 ppm
σ22 = 4 ppm
σ33 = -51 ppm
σ11 = 68 ppm | 64 ppm
σ22 = -12 ppm | -8 ppm
σ33 = -84 ppm |-91 ppm
σ11 = 77 ppm
σ22 = 14 ppm
σ33 = -168 ppm
31P Spectraωr/2π = 12 kHz
B0 = 7.1 T
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1D 1H Spectra at 18.8 T1D 1H Spectra at 18.8 T
MP
(MP)2
MPpoly
1H SpectraMAS
ωr/2π = 49 kHzB0 = 18.8 T
ωr/2π = 12 kHzB0 = 7.1 T
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Heteronuclear Correlation 1H-31PHeteronuclear Correlation 1H-31P
1H
31P
MPωr/2π = 12 kHz
ττττct = 0.1 ms ττττct = 2.5 ms
31P
1H
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Heteronuclear Correlation 1H-13CHeteronuclear Correlation 1H-13C
ωr/2π = 12 kHzB0 = 7.1 T
13C
1H
1H Spectrum
B0=18.8 T
13C
1H
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Homonuclear: 15N-15N in MPHomonuclear: 15N-15N in MP
ωr/2π = 12 kHzB0 = 7.1 T
N9/N10
N6/N7
N11
N8
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15N-1H distance measurements15N-1H distance measurementsDipolar recoupling Echo: refocus 15N chemical shift,
keep 15N-1H dipolar interaction
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MP: AssignmentMP: Assignment
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Hydrogen Bonding & π−π StackingHydrogen Bonding & π−π Stacking
MP MPyro MPpoly
Combined NMR and X-ray Powder
Diffraction
V. Brodski, R.Pescharand H. Schenk
Univ. Of Amsterdam
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Hydrogen bonding in biological molecules
Hydrogen bonding in biological molecules
17O is a quadrupolar I=5/2 nucleus
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Quadrupolar InteractionQuadrupolar Interaction
+++
++ +
+
+
−−Spin > 1/2
( ))(
)12(4
3)(with
ˆˆˆ3)(ˆ :ionapproximatsecular
,
2,
θθω
ωθ
ZZjjj
jj,Q
jjjzQjj
Q
VII
eQ
IIIH
−=
⋅−=
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First order quadrupolar interactionFirst order quadrupolar interaction
(Hz)-100000100000 -200000200000 0
a
b
c
Qω /2π
d
e
23Na (I=3/2) in NaNO3
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Second order quadrupolar interactionSecond order quadrupolar interaction
As Coordinations in AlGaAs
75As NMR @ 18.8TAl0.47Ga0.53As
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What Information Can NMR GiveWhat Information Can NMR Give
Site Identification
•Quadrupolar Interaction�Determination of local symmetry (distortions).�17O NMR parameters are sensitive to H-bond formation.�Majority of periodic table has I>1/2
www.pascal-man.com
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Cqc
c(M
Hz)
Li
Na
KRb
Cs
Quadrupolar Interaction: Site Symmetry
Quadrupolar Interaction: Site Symmetry
Framework aluminosilicate glasses with varying charge-balancing cations (Li, Na, K, Rb, Cs)Dirken, Nachtegaal and Kentgens, Solid State Nucl. Magn. Reson. 5 (1995) 189.
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Tool: Magic Angle SpinningTool: Magic Angle Spinning
~ 1/B0
spin-½ spin>½
P2 P4
ωωωωr/2ππππ=12 kHz
ωωωωr/2ππππ=870 Hz
static
[13C2]-glycine
(13C)
fast magic-angle spinning
not averagedaveraged
Use high fields !
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Tools: Double Rotation (DOR)Dynamic Angle Spinning (DAS)Tools: Double Rotation (DOR)Dynamic Angle Spinning (DAS)
))(cos(),(),())(cos(),(),(),( 44422200, θβαυθβαυυυ PmICPmICmICmm ⋅⋅+⋅⋅+⋅=−
1 2 3 4 5
10°
30°
50°
70°
90°
k = t2/t1
θ2
θ1
Mechanicallyinvolved
DedicatedHardware needed
Samoson, Lippmaa and Pines, Mol. Phys. 65 (1988) 1013. / Llor and Virlet, Chem.Phys.Lett. 152 (1988) 248.Mueller, Baltisberger, Wooten and Pines, J. Phys. Chem. 96 (1992) 7001.
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Multiple-Quantum MASMultiple-Quantum MAS
Frydman and Harwood, J.Am.Chem.Soc. 117 (1995) 5367
SHEARING
Sensitivity issue (multiple-quantum excitation and conversion)
))(cos(),(),())(cos(),(),(),( 44422200, θβαυθβαυυυ PmICPmICmICmm ⋅⋅+⋅⋅+⋅=−
MAS
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27Al MQMAS
�High Field (14.1 T)
�Fast MAS (27 kHz)
�MQ→1Q DFS conversion
1.0
4.16
55
=
==
η
σMHzC
ppm
qcc
iso
Dehydrated H-ZSM5Dehydrated H-ZSM5
Kentgens, Iuga, Kalwei and Koller, J.Am.Chem.Soc. 123 (2001) 2925.
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rDFS 17O MAS NMR rDFS 17O MAS NMR
17O challenging because of low γ and large CQ~4.3 S/N Enhancement for biologically relevant material
17O MAS (25 kHz) @ 14.1T 1968 transients
Experiments:δiso= 87 ppmCQCC= 8.52 MHzη=0.74
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Heteronuclear Recoupling:17O-1H distance measurement
Heteronuclear Recoupling:17O-1H distance measurement
rOH distance 104 pm is within 5% of the distance determined by neutron diffraction (99 pm).
O-H libration slightly averages dipolar interaction.
A. Brinkmann & A.P.M. KentgensJ. Phys. Chem. B 110 (2006) 16089
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Heteronuclear Recoupling:17O-1H distance measurement
Heteronuclear Recoupling:17O-1H distance measurement
H’’
Hη
rO-H’’ distance 161 pm
A. Brinkmann & A.P.M. KentgensJ. Am. Chem. Soc. 128 (2006) 14758
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Summary of Internal HamiltoniansSummary of Internal Hamiltonians
int^
MAGNETIC(all spins)
ONE-SPIN TWO-SPIN
ELECTRIC (spin >1/2 only)
CHEMICALSHIFT
SPIN-ROTATION
DIPOLE-DIPOLE
J-COUPLING
QUADRUPOLECOUPLING
Malcolm H. Levitt, Spin Dynamics, Wiley, 2001
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ConclusionsConclusions�Solid state NMR is a powerful analysis technique
�Probes microscopic interactions (1-100Å)�Study structure and dynamics
�Works in crystalline, partly disordered and amorphous compounds
�Non-destructive technique needing no special sample preparation
�Novel methodological developments will open new applications in advanced materials science
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Sensitivity enhancement is driving methodological developments
Sensitivity enhancement is driving methodological developments
Options for signal enhancement: Potential gain• Double B0 3• Cryo-cooled rf coils 3• Population transfer in coupled or quadrupolar spin systems 2-5
• Low temperature MAS 10• Microcoil detection 100• Dynamic Nuclear Polarization (DNP) 103
• Optical polarization (ODMR / OPMR) 104
• Hyper polarized Xe, He, Kr 104
• Para-Hydrogen 104
• Force detection 103-106
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• 33 T• 40 kA • 20 MW
14 T600 MHz
18.8 T800 MHz
SSNMR Beyond 1 GHzSSNMR Beyond 1 GHz
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Opportunities and ProblemsOpportunities and Problems
� Sensitivity (~B7/4)� Resolution (~B - B2)� High speed (proton) MAS� Quadrupolar nuclei
Opportunities� Intrinsic homogeneity (~10-3/cm)� Temporal stability (~10-5)
�power supply� temperature and flux
changes� Operation time
Problems
� Ferro-shims� High speed MAS� Reference deconvolution� Follow-B
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Field profile of a uniformly magnetized cylinder
Field profile of a uniformly magnetized cylinder
Field profile Ferroshim
Magnet field profile before and after Ferroshim
Shifting the shim off-axis allows reduction of radial gradientsMagic Angle Spinning averages residual gradients
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Field map D2O, after x-y optimization ferroshimField x-y gradient < 5 kHz (drift dominated) <25 ppm/cm
Field map with ferroshimField map with ferroshim
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Distorted spectrum
Reference signal ofdifferent nucleus
Deconvoluted spectrum
S
I
t
tttc
γγ
×=−
−
)(S)(W)(S
)(refexp
refideal
)]()(S[FT)( exp tctSc ×=ω
Reference DeconvolutionReference Deconvolution
Morris, Barjat and Horne, PNMRS 31 (1997) 197-257.
Metz, Lam and Webb, Concepts Magn. Reson. 12 (2000) 21-42.
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Reference DeconvolutionReference Deconvolution
� Discrete field steps� MAS: resolution is stability limited� Fourier spectrum distorted (chirp)� Length of FID determines resolution
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Triple-tuned MAS probe2D reference channel
Triple-tuned MAS probe2D reference channel
D
k H z1 2 0 1 2 0 . 5 1 2 1 1 2 1 . 5 1 2 2 1 2 2 . 5 1 2 3
- 5
0
5
1 0
x 1 07
D
T i m e ( µ s )0 0 . 5 1 1 . 5 2 2 . 5 3
x 1 04
- 2
- 1
0
1
2
x 1 04
ND4Cl reference signal lasts 30 - 50 msec, i.e. intrinsic homogeneity of about 0.15 ppm.
Jan van BentumErnst van EckJan van Os
Probe technology:Ago Samoson
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ppm C
sca
n
Field stability
-1000100200300
0
0.5
1
1.5
2
x 104
Field stability 10-50 ppm on 13C
Field StabilityField Stability13C MAS of alanine
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©Follow B option©Follow B option
� Use first 200 µsec of reference FID to determine field� Reset spectrometer frequencies � Use remaining part of ref-FID for deconvolution
BBBB
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Follow B + reference deconvolution
Follow B + reference deconvolution
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Bruker News and EventsAVANCE 900, first resultsBruker News and EventsAVANCE 900, first results
At 21.1 T separation of the two Sc sites is nearly achieved…
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1: Cq=15.4 MHz ηQ=0.612: Cq=23.4 MHz ηQ=0.10
Intensity ratioexp 1:2.995theor 1:3
Sc2O345Sc 309.5 MHz
64 scansMAS 38 kHzFixed phaseAveraging=> followB=> Ref. dec.
Systems with largequadrupolar interactions
Systems with largequadrupolar interactions
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Hydrogen storageHydrogen storage
32 MJ/ltr 13 MJ/ltr 10 MJ/ltr 8 MJ/ltr 2.4 MJ/ltr
gasoline Mg 2NiH4 LaNi 5H6 H2 liquid H 2 gas (200 bar)
� Solid H2 storage� (Complex) Metal hydrides,
like NaAlH4, NaBH4, LaNi5H6.
� Important technical issues are weight, volume, discharge/recharge rates, reaction heat, safety and cost
� IEA (International Energy Agency) targets: � at least 5-10 wt.% � H2 recoverable at < 80°C � Loading/unloading at 1 atm absolute pressure.
NaAlH4 ↔ Na3AlH6 + 2 Al + 3 H2
Na3AlH6 ↔ 3 NaH + Al + 3/2 H2
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Static 1H NMR on Ti-doped NaAlH4Static 1H NMR on Ti-doped NaAlH4
� Partly release of H2 -> NaAlH4 and Na3AlH6 are present
� Hahn-Solid-Hahn Echo to avoid spectral distortions� Two fractions with different relaxation times T1 and
different line widths.� Na3AlH6: Narrowing of the line shape -> proton
mobility in the crystal -> fast rotating AlH6 clusters
Spectrum
Fit
NaAlH4 FWHM = 42.0 kHz, T1 ~ 20s
Na3AlH6 FWHM = 13.3 kHz, T1 ~ 8s
NaAlH4 ↔ Na3AlH6 + 2 Al + 3 H2Na3AlH6 ↔ 3 NaH + Al + 3/2 H2
Margriet Verkuijlen, Jan van Bentum
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1H and 27Al high-speed (40 kHz) MASof Ti-doped Alanates at 30 T
1H and 27Al high-speed (40 kHz) MASof Ti-doped Alanates at 30 T
NaAlH4
Na3AlH6
Al27Al MAS NMR
M. Verkuijlen, E. van Eck, J. van Bentum,B. Dam (Free University of Amsterdam)
C. Baldé, K. de Jong (Utrecht University)
NaAlH4 ↔ Na3AlH6 + 2 Al + 3 H2
Na3AlH6 ↔ 3 NaH + Al + 3/2 H2
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SR662
90° 90° 90°
2H
13C
τmixt1 t2
synchronize synchronize
36τr
18060 180-60
2τr
SR662-RFDR
[R662]240[R66
2]0 [R66-2]0 [R66
2]120 [R66-2]120 [R66
-2]240 [R66-2]240
Broadband homonuclear recouplingBroadband homonuclear recoupling
Andreas Brinkmann, Jorge Garibay
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13C-13C homonuclear correlation13C labeled L-alanine
13C-13C homonuclear correlation13C labeled L-alanine
τm= 3.6 ms
SR662
90° 90° 90°
2H
13C
τmixt1 t2
synchronize synchronize
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13C-1H heteronuclear correlation
of L-alanine
13C-1H heteronuclear correlation
of L-alanine
CH3
CH
NH2OH
CP match ν1C=70 kHz; ν1H=30kHz; νr=40 kHz
Contact time 50µs Contact time 1ms
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Conclusion High Field NMRConclusion High Field NMR
�Using a combination of hardware solutionsand NMR tricks, one- and two-dimensionalsolid-state NMR at 30 Tesla is feasible.
�Quadrupolar systems with either very large orvery small quadrupolar interactions
�High resolution proton NMR
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AcknowledgementsAcknowledgements
Physical Chemistry / solid-state NMRJan van Bentum
Ernst van Eck
Andreas BrinkmannJorge Villenueva Garibay
Paul KnijnMargriet VerkuijlenSureskumar Vasa
Chandrakala GowdaAnna-Jo de Vries
Gerrit JanssenJan van Os
Hans Janssen
Universiteit TwenteHan Gardeniers
Jacob Bart
KBFI TallinnAgo Samoson
Tiit AnupoldJan Paast
Free University of AmsterdamBernard Dam
Ronald Griessen
University of UtrechtCees Baldé
Krijn de Jong
ETH ZürichJeroen van Bokhoven
Roel Prins
IMM groups of
Jan-Kees Maan
Rob de GrootGilles de Wijs
Floris RutjesJan van HestAlan Rowan
Roeland Nolte
TechnoCentrumE. Sweers
B. van den Berg