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Spin pumping and spin transport in magne0c metal and insulator
heterostructures Eric Montoya
Surface Science Laboratory Simon Fraser University
Fe
Au
Fe Au
YIG
Au
Fe Au
Magne0c metal Magne0c insulator
Why use spin currents? We can eliminate circumvent these problems: • Joule Hea0ng • Circuit Capacitance • Electron migra0on
Outline: • Introduce spin pumping • Spin transport in Au • Spin pumping from magne0c insulator (if 0me)
Spin Dynamics (LLG) Landau Lifshitz Gilbert
γω
α=ΔH
Ferromagnetic Resonance (FMR)
FMR linewidth:
sMGγ
α =
Anritsu signal generator: 1-70 GHz electromagnet: 2.8 T
Bulk damping is noise in spin orbit (s-o) interaction Interface damping is spin pumping
Heff
M !
36GHz
∂
�M
∂t= −γ
��M ×
�Heff
�+ α
��M × ∂
�n
∂t
��n =
�M
Ms
NMFM1 FM2
0 Lx
�I �m
�mNM
�I �m
=−gµB4πMs
Re [g↑↓]
��M × ∂n̂
∂t
�⊗ x̂ ∂
�M
∂t=
1
dFM
∂�m
∂t
�m =
−gµB�
�S
Re [g↑↓] =1
2
�
n
[|r↑,n − r↓,n|2 + |t↑,n − t↓,n|2]
|r↑(↓),n|2 + |t↑(↓),n|2 = 1 r↑,n∗
r↓,n + t↑,n∗
t↓,n � 0
g↑↓ =�
n
[1− Re[r↑,n∗
r↓,n + t↑,n∗
t↓,n��
≈ kF2
4π∼ N2/3
Spin Pumping
Spin mixing conductance for metals
Density of electrons per spin direc0on in NM
Spin current arises from the 0me retarded response to interlayer exchange coupling The spin current can be expressed as an accumulated magne0c moment (/area)
NMFM1 FM2
0 Lx
�I �m
�mNM
Spin Pumping
�I �m
=−gµB4πMs
Re [g↑↓]
��M × ∂n̂
∂t
�⊗ x̂ ∂
�mNM∂t
= D∂2
�mNM∂x2
− 1τsf
�mNM
D =vF 2τm
3
Boundary FM1/NM FM1/NM/FM2
x = 0�I �m− 12vF
�mNM = −D ∂
�mNM∂x
x = L ∂�mNM∂x = 0 −D
∂�mNM∂x =
12vF
�mNM
The accumulated magne0c moment then diffuses away from then interface
δsd = vF
�τsfτm3
0 100 200 300 400 500 6000
3
6
9
dAu !AL"
Α10"3s"
!sf is only unknown parameter sf is only unknown parameter
Spin Pumping Theory
Fsd=F(!sf, !m, dNM, vF)×Fb sf, !m, dNM, vF)×Fb Fb=F(dFM, 4"MS, g⇅, g, #B)
• GaAs(001) Template – Atomic H etching – 650eV Ar+ spu^ering (con0nuous rota0on)
– 4x6 reconstruc0on RHEED monitored
• 16Fe and 12Fe have different FMR fields
• At 16Fe FMR, 16Fe acts as spin pump and 12Fe acts as spin sink GaAs(001)!
16Fe (2.3nm)!
12Fe (1.7nm)!20Au (4.1nm)!
300Au (61.2nm)!or!
20Au (4.08nm)!
Single Layers
Double Layers
Sample Growth by MBE
• Van der Pauw measurements – 10K-‐300K
• Contribu0on due to bulk phonon and interface sca^ering
• Using Mathiassen’s Rule:
• Interface sca^ering
contribu0on independent of temperature
1
τm=
1
τp+
1
τi
τm =σmene2
!
R88295 = 2.5
!
R10295 = 6.1
Charge Transport
Ferromagne0c Resonance
• FMR followed Gilbert damping phenomenology:
• Enhanced Gilbert damping due to spin pumping is an interface effect
• Spin momentum accumulates at the Fe/Au interface
∆H(ω) = αω
γ+∆H(0)
��
��
��
��
�� �
�
��
��
�� �
�� �
��
�
�
��
�
�
0 10 20 30 400
50
100
150
f �GHz�
�H�Oe�
Gilbert Damping
• $sp greatest in ballis0c limit for sp greatest in ballis0c limit for double layer
• $sp increases with decreasing sp increases with decreasing temperature for double layers
• $sp decreases with decreasing sp decreases with decreasing temperature for single layers
100 150 200 250 3000
3
6
9
Temperature !K"
Α!10"3 "
20Au DL
20Au SL
300Au SL
300Au DL
Relaxa0on parameters
0 50 100 150 200 2500.0
0.5
1.0
1.5
2.0
2.5
Temperature �K�
Τ�10�13
s�
τsf(290K)
τp(290K)= 8.4
τsf(90K)
τp(90K)= 22.1
• !sf increases faster than !p sf increases faster than !p as temperature decreases
• !i very weakly dependent on temperature
Spin flip sca^ering dominated by phonon processes
Combined influence of temperature dependent spin flip sca^ering at interfaces and bulk phonon sca^ering?
or Mul0-‐phonon sca^ering that does not contribute strongly to
resis0vity?
Previous Studies
three fitting parameters remained: S↑ ,S↓, and Pvac/Au. Unfor-tunately a unique fit to the data was not achieved with thedata in Fig. 6 alone.
The magnetoresistance data from Au/Fe/Au/Fe/GaAs!001" was used to help determine the specularity pa-rameters. A necessary simplifying assumption that all Fe/Auinterfaces had the same degree of specularity !S↑ and S↓"reduced the number of fitting parameters. The reflectivity atthe outer Au interface Pvac/Au was first set to zero, and thenall possible combinations of S↑ and S↓ that gave the correctconductivity for a parallel and antiparallel configuration inthe Au/Fe/Au/Fe/GaAs sample were determined, as shownby the curves joining the two sets of triangles in Fig. 7. Thepoints where these curves intersected gave the correct mag-netoresistance. The calculation was repeated for Pvac/Au=0.25 and 0.50. The points of intersection for the variousPvac/Au lay roughly on straight lines, shown by the twodashed lines in Fig. 7. The specularity parameters decreasedapproximately linearly with increasing Pvac/Au. The GMRdata alone indicated that the reflection from the outer Auinterface was mostly diffuse, Pvac/Au!0.5, and one spinchannel had a specularity in the range 0.6"S"0.8.
Fits to Au conductivity data in Fig. 6 were subsequentlyconstrained by the requirement that the parameters P ,S↑ andS↓ produce the correct magnetoresistance for Au/Fe/Au/Fe!lines A and B in Fig. 7". P=0 gave the best fit to the Auconductivity. The solid line in Fig. 6 represents the fit to thedata using either !P=0.0, S↑=0.55, and S↓=0.77" or !P=0.0, S↑=0.83, and S↓=0.53". When P was increased, the #2also increased. The dashed line in Fig. 6 represents !P=0.41, S↑=0.03, and S↓=0.65", the fit having the highest #2!satisfying the constraint of line A in Fig. 7". The results ofthe fits are displayed in Table II. A lower $Au would haveresulted in larger specularity parameters.
The diffuse scattering modeled by S↑ and S↓ describe theinfluence of interface imperfections. Unfortunately, no calcu-
lations or measurements were available for the spin asymme-try of Au impurities in Fe for comparison to the fits. It was,however, interesting to compare the spin asymmetry of diluteCu and Ag impurities in Fe since these elements were iso-electronic with Au and therefore were expected to scatter in asimilar fashion. Mertig recently calculated a spin asymmetry%↓ /%↑=8.20 for Cu and 12.22 for Ag.25 This would suggestthat Au defects at the Fe/Au interface would also diffuselyscatter minority electrons more strongly. Based on this argu-ment, one tends to favor the parameters from line A.
The fit of the Au thickness with first-principles calculationdescribed the data well for large thicknesses, but failed todescribe the conductivity for small thicknesses, in particularthe 5 ML Au film. One had expected a drop in the conduc-
FIG. 6. In situ measurement of the conductivity as a function ofAu thickness deposited on 28 ML Fe/GaAs!001". The two curvesare calculated using first-principles density functional calculations.The solid line !P=0, S↑=0.55, S↓=0.77" is the best fit given the setof parameters described by line A in Fig. 7 below. The dashed line!P=0.41, S↑=0.03, S↓=0.65" has the highest #2 among the param-eters on line A, which demonstrates the sensitivity of the fit to thefitting parameters.
FIG. 7. Fitting of the conductivity of 20 ML Au/10 MLFe/7 ML Au/28 ML Fe/GaAs!001" using first-principles calcula-tions. The filled points correspond to the parameters which give thecorrect sheet resistance for a parallel configuration of magnetic mo-ments !resistance at saturation in Fig. 2" and the open points givethe correct sheet resistance for an antiparallel !zero applied field"configuration. The triangles, diamonds, and squares are calculatedfor Pvac/Au=0, 0.25, and 0.5, respectively. The dashed lines labeledA and B are interpolations of the points of intersection which givethe correct GMR.
TABLE II. The GMR fitting parameters determined from Fig. 7that gave the best fit to the thickness dependence of the Au conduc-tivity shown in Fig. 6. The confidence interval column !CI" shownfor each set of solutions A and B was the range of the specularityparameters within the 90% confidence interval of the fit. The 90%confidence interval is a region in the parameter space of #2 where90% of experiments will be fitted by a set of parameters fallingwithin that region.
Best fit !A" CI !A" Best fit !B" CI !B"
P 0.0 0.0–0.16 0.0 0.0–0.20S↑ 0.55 0.55–0.34 0.83 0.83–0.74S↓ 0.77 0.77–0.72 0.53 0.53–0.32
MONCHESKY et al. PHYSICAL REVIEW B 71, 214440 !2005"
214440-8
single magnetic layer structure F/NM the boundary condi-tions at the F/NM interface are5
jm − 0.5vFmNM = − D!mNM
!x. !5"
For the outer interface we used a free magnetic moment con-dition
!mNM!x
= 0. !6"
For a magnetic double layer structure F1/NM/F2 the bound-ary conditions at the F1/NM interface are equivalent to Eq.!5". The boundary conditions at the NM/F2 interface are5
−!mNM
!x= 0.5vFmNM. !7"
The boundary conditions in Eq. !7" are valid for the casewhen the layer F2 is off resonance and therefore contributesnegligibly to spin pumping. The coefficient 0.5 correspondsto the effective transmission coefficient from the NM to Flayers and is given by Eq. !13" in Ref. 5. The right hand sideof Eq. !7" represents the magnetic current from NM into F2and acts as a driving field for the magnetic moment in F2.
The purpose of the studies presented in this paper was toidentify the spin diffusion coefficient and spin flip relaxationtime in Au. We carried out two experiments. D and !sf weredetermined by FMR employing a single magnetic structureF/NM. Similar experiments were done by Mizukami et al.6
on the Cu /permalloy /Cu /Pt films. In addition the propaga-tion of spin current in NM was investigated by time andspatial resolved Kerr effect technique. For this case we useda double magnetic layer F1/NM/F2 where F1 was used forspin pumping and the layer F2 was used as a detector of thespin current.
The Fe films were deposited at room temperature on acommonly used 4"6-GaAs!001" reconstructed template.The 4"6 surface reconstruction was obtained by annealingthe GaAs wafer at #600 °C following hydrogen cleaningand Ar+ sputtering at 650 eV. The following structures weregrown: !a" nAu /16Fe /GaAs!001", where n=20, 80, 150,200, 250, 300 and the integers represent the number ofatomic layers; and !b" 20Au /12Fe /300Au /16Fe /GaAs!001"and 20Au /12Fe /300Ag /16Fe /GaAs!001".
The FMR studies were carried out using standard micro-wave spectrometers using 10, 24, 36, and 73 GHz, see de-tails in Ref. 7. For both bulk and interface Gilbert damping#H is strictly linearly dependent on the microwave angularfrequency $, #H=%!$ /&".
The NM layer increases magnetic damping when itsthickness becomes comparable to the spin diffusion length'sd=vF!!sf!el /3"0.5. For dNM('sd#H is given only by theintrinsic Gilbert damping of the Fe layer. For dNM)'sd the#H increases by the loss of spin momentum in NM. Theequations of motion !1" and !4" with the boundary conditions!5" and !6" were solved self-consistently, and were employedfor fitting the measured spin pumping coefficient %, see Fig.1. The spin pumping Gilbert damping parameter, %sp, as afunction of the Au thickness was fitted with the following
parameters: %intr=3.5"10−3, g̃↑↓=2.4"1015 cm−2, !el=1.2"10−14 s, !sf=15"10−14 s, and the Fermi velocity was as-sumed to be *F=1.4"108 cm /s. The fitted parameters resultin the spin diffusion length 'sd of 34 nm. It is interesting tonote that Kurt et al.8 studied the spin diffusion length byusing current–perpendicular-to-plane !CPP" giant magnetore-sistance !GMR" measurements using polycrystalline Au /Cuspacers. They obtained 'sd=35 nm, which is very close toour result. The ratio r=12.5 indicates that in our samples !sfis one order of magnitude larger than !el.
20Au /12Fe /nAu /16Fe /GaAs!001" structures were em-ployed in the study of propagation of spin currents across theNM film. Time-resolved magneto-optical Kerr effect!TRMOKE" measurements are an ideal tool for investigatingthe propagation of spin currents in these structures. Strobo-scopic measurements of magnetization precession in the10 GHz frequency range were carried out with picosecondtime resolution and submicrometer spatial resolution, using acoplanar transmission line carrying repetitive picosecondmagnetic excitation pulses. After excitation the 100 fs dura-tion laser pulses probed the top 12Fe layer via the perpen-dicular component of precessing magnetization !polarMOKE" at the delay time tD, see detailed description in Ref.9. Spin currents generated by the bottom 16Fe layer propa-gated across the normal metal spacer and resulted in rf exci-tations of the top 12Fe film. The resonant frequencies of theFe layers are strongly affected by the interface anisotropies,see Ref. 10. Therefore the 12Fe and 16Fe films have theirresonant frequencies 4.5 GHz apart and therefore the spincurrent induced magnetization precession in the 12Fe filmcan be in principle easily distinguished. However, the iden-tification of absorbed spin current is complicated by the pres-ence of a direct TRMOKE signal from the bottom 16Fe layerwhich becomes observable when the spacer thickness is lessthan 250 atomic layers. A Au spacer with the thickness of300 atomic layers was sufficient to suppress the signal fromthe bottom 16Fe film. No measurable MOKE signal was ob-served on the 300Au /16Fe /GaAs!001" sample. Therefore,further studies with the Au spacer were carried out using the20Au /12Fe /300Au /16Fe /GaAs!001" structure. The timedependence of the picosecond resolved Kerr signal and itsfast Fourier transform !FFT" are shown in Figs. 2!a" and
FIG. 1. Dependence of the additional damping by spin pumping, %sp, on theAu cap layer thickness dAu in the Au /16Fe /GaAs!001" samples. The !•"symbols represent the measured data from the #H dependence on micro-wave frequency f , #H!f". #H!f" followed well a linear dependence on f .The error bars were determined from small slope variations in the #H!f"measurements. The solid line shows fitting using the spin pumping theorywith the following parameters.: g̃↑↓=2.4"1015 cm−2, !el=1.2"10−14 s, and!sf=15"10−14 s.
07C509-2 Kardasz et al. J. Appl. Phys. 103, 07C509 "2008#
Downloaded 19 Apr 2011 to 142.58.93.159. Redistribution subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions
T. Monchesky et. al. Phys.Rev.B. 71 (2005) B. Kardasz et. al. J.Appl.Phys. 103 (2008)
From 80-‐5nm thickness of Au !i increases by a factor of 12 !sf only increases by a factor of 1.5 sf only increases by a factor of 1.5
!sf can only weakly be dependent on interface sca^ering sf can only weakly be dependent on interface sca^ering
Temperature dependence of !sf governed by mul?-‐phonon scaAering sf governed by mul?-‐phonon scaAering
Spin pumping at YIG/Au interface
recently new ideas and systems being developed for generation of pure spin currents for driving Spin Transfer Torque (STT) devices
John Slonczewski has shown higher spin efficiency can be achieved by thermal gradients
using Magnetic Insulator (MI)/NM heterostructures
new emerging field spincoloritronics
Arne Brataas and Gerrit Bauer have shown that the spin pumping generation is determined at MI/NM interfaces by spin mixing conductance
?????what is at the YIG/Au interface ????
!
g"#
J. Slonczewski, PRB 82, 054403 (2010)
!
g"# =
1
2| r
n
" $ rn
#|2 + | t
n
" $ tn
#|2( )
n
%
!
tn
"#= 0
!
rn
"#=1$ e
i%n"#
g!" = 1# cos(!n! #!
n
")( )
n
$
B. Heinrich et al. PRL, 107, 066604 (2011) C. Burrowes et al. APL , 100, 092403 (2012)
Spin mixing conductance in magne0c insulators
XPS
YC
O Fe
YIG surface chemistry
YIG: Y3Fe2(FeO4)3
• Grown on (111) Gd3Ga5O12 substrate by PLD at 700C and 0.1Torr O2
• Thickness d=9nm (low angle XRD) • 4"Ms=1.31kG(SQUID), g=2.027 Ms=1.31kG(SQUID), g=2.027
(FMR) • Surface roughness 0.5nm (AFM)
As prepared YIG has surface deficiency of Fe
Common for even thick
PLD prepared YIG
!!
!
!
0 10 20 30 400
10
20
30
40
50
60
frequency !GHz"
!H!Oe"
7.3 7.6 7.9
H !kOe"
Amplitude!a.u."
#a$
7.3 7.6 7.9
H !kOe"Amplitude!a.u."
#b$9nmYIG 9nm YIG/6.1nm Au/4.3nm Fe/6.1nm Au
g!" #1.3$1014cm
%2
12% efficiency compared to Fe
Spin pumping from YIG
∆H = 15.9Oe ∆H = 21.2Oe Transfer of angular momentum to Fe layer is seen as
loss of angular momentum in YIG layer
Damping!
Evalua0ng in Ar+ etched YIG
�� ��
�
�
�
�
0 10 20 30 400
20
40
60
80
100
120
f �GHz�
�H�Oe�
9YIG(etched)/6.1Au
9YIG(etched)/6.1Au/4.3Fe/6.1Au
! = 0.0069
! = 0.0014
g!" = 5.1#1014cm
$2
g!"
Low angle Ar+ etched 10minutes
0.8kV, 400o C
70% of predicted by first principles calculations
X. Jia et al. Europhysics Letters 96, 17005 (2011)
50% of Fe/Au
!"#$"#%&'#()%*&+(,-&
./01.&2(&
34&5&& 34&5&
./01.&2(&678&
698&
6:8&
6$8&
metallic state of Fe decreases rapidly g!" # 3.7$10
14cm
%2
required change for increased g!"
XPS on YIG
740 735 730 725 720 715 710 705 700
XPS
signa
l
Eb [eV]
Prolonged etching lead to metallic Fe -‐> Suppresses pumping
Conclusions:
spin pump/sink effect can be used to investigate the spin transport parameters in magnetic nanostructures
spin pumping at YIG/Au is efficient 70% of theory calc. 50% of Fe/Au
evidence that a time retarded interlayer exchange coupling creates spin pumping
Efficiency of spin pumping comparison Microwave driven: for f=10GHz and Θ=90o 2x1010 Thermal excitation: for ΔT=10 K , Vcoh=2.7x103 nm3 ωeff=2x102 MHz 1.0x108 STT (60% polarization): for 2x106 Acm-2 : 2x1010
!
!
4!"g!"sin
2# !
4!g!"!
2kBTYIG
m #TAu( )
VcohM
s
$
%
&&
'
(
))
!eff = "2kB TYIG
m !TAu( )VcohM
s
"
#
$$
%
&
''
J. Xiao et al. PRB 81, 214418 (2010)
nm-2
Acknowledgements: NSERC, CIfAR , NSF, NIST
Simon Fraser University Physics, Magnetism
Prof. Mingzhong Wu, Dr.Young-Yeal Song, and Dr. Yiyan Sun
Physics Department Colorado State University
Fort Collins, USA
Ken Myrtle Research Assistant
Dr. Bartek Kardasz research associate
Dr. Erol Girt Professor
Dr. Capucine Burrowes PDF
Dr. Bret Heinrich Prof. Emeritus
artist: Mr. Clarence Mills Charles Eyrich MSc Candidate
Dr. Monika Aurora PhD Candidate
Eric Montoya PhD Candidate
Dr. Wendell Huttema PDF
Conclusions Temperature dependence of !sf sf
from 290K to 90K
!sf increases by factor of 10 sf increases by factor of 10 !p increases by factor of 4 !i negligible dependence
Temperature dependence of !sf governed by mul0-‐phonon sca^ering sf governed by mul0-‐phonon sca^ering
Thickness dependence of !sf sf
from 80nm to 5nm !sf increases by factor of 1.5 sf increases by factor of 1.5
!p constant !i increases by factor of 12 i increases by factor of 12
deposition of Fe on bare YIG results in metallic state of Fe
no spin pumping
YIG surface H atom etching showed in XPS a strong presenceof metallic state of Fe
no spin pumping
spin current blockade by metallic Fe
704 708 712 716
Binding Energy [eV]
704 708 712 716 720
Binding Energy [eV]
metallic state of Fe
1 MLFe deposited at 500o C
YIG state of Fe