Quantum effects in Magnetic Salts Part II G. Aeppli London Centre for Nanotechnology.
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Transcript of Quantum effects in Magnetic Salts Part II G. Aeppli London Centre for Nanotechnology.
Quantum effects in Magnetic Salts Part II
G. Aeppli
London Centre for Nanotechnology
London Centre for NanotechnologyLondon Centre for Nanotechnology
Talk 1
• TF Ising model in 3d shows interesting QM effects in real experiments
• ‘slaved’ degrees of freedom which are classically irrelevant can have qualitative quantum impact
outline
Introduction – saltsquantum mechanicsclassical magnetism
RE fluoride magnet LiHoF4 – model quantum phase transition
1d model magnets
2d model magnets – Heisenberg & Hubbard models
collaborators
• G-Y Xu (BNL)• C.Broholm (Hopkins)• J.F.diTusa(LSU)• H. Takagi (Tokyo)• Y. Itoh(Tsukuba)• Y-A Soh (Dartmouth)• M. Treacy (Arizona)• D. Reich (Hopkins)• D. Dender (NIST)
Example #2 - Heisenberg antiferromagnet
• H=JSiSj with J>0
• classical ground state
Consider commutator again
Mfm=Szl (ferromagnet)
Maf=(-1)l Szl (antiferromagnet)
[M,H]=... (-1)l([Szl,Sl](Sl-1+Sl+1)
-([Szl-1,S l-1]+[Sz
l-1,S l-1])Sl)
for FM, [M,H]=0 while not so for AFM
Antiferromagnets can self-destruct
does the classical picture ever go wrong- look at spin wave
amplitudes |<Q|S+|0>|2
• Diverge as 1/Q when Qmagnetic zone center for AFM
• ~ constant for FM
Break-down of S-W theory
• <M2>=S(S+1)=static piece + fluctuating piece
• <M2>= Mo2+ (E-Eo(Q))|<Q|S+|0>|2 dEddQ
=Mo2+ (1/Q)ddQ(AFM) (Mo=ordered moment)
• clearly a problem for AFM in d=1
>,
<> - >
> + >J
Consequence- antiferromagnetism can be
unstable, especially for low d
What do experiments say?
S=1/2 chain AFM (CuGeO3)
S=1/2 for zero field
No magnetic orderpairs of fermionic excitations rather than harmonic spin wavesbut at first sight, difficult to distinguish from multimagnon series
expansion...
Want something qualitatively different…
For a conventional antiferromagnet in a field, only
rounding effects, both types of modes have peak intensity at
-1 -0.5 0 0.5 1
1||B
B
Dender et al., Phys. Rev. Lett. 79(9), pp. 1750-1753, (1997)
E=0.21meV
Dender et al., Phys. Rev. Lett. 79(9), pp. 1750-1753, (1997)
Zeeman-split spinon Fermi surface
Dender et al., Phys. Rev. Lett. 79(9), pp. 1750-1753, (1997)
Consider S=1 AFM chain compound YBaNiO5
S(Q)=S<SlSm>expi|l-m|Q
equal-time correlationfunction = liquid structure factor
no AFM order, only fluctuations
width =1/xo where xo~7a
An unstable antiferromagnet
0
20
40
60
0 0.5 1 1.5 2
q
h (
meV
)
Xu et al, unpublished
a gapped ‘spin liquid’(Haldane)
Why?
rationalization #1 Sz=-1,0,+1 -+-+-+0-+-+-+0-0+-+-+ (‘floating zeroes)
rationalization #2(‘valence bond solid’)- consider JHund<JNi-Ni
Ni +2
Just a simple liquid?
secret order(quantum coherence) in explanations, but apparently not visible in the equal-time two-spin
correlation function <0|S-
-q S+q|0>= S(q,
can we measure coherence length for this new state?
0
20
40
60
0 0.5 1 1.5 2
q
h (
meV
)
S(q
,
S(q
,
m
eV)
Xu et al, unpublished
Theory by Sachdev et alXu et al, unpublished
Mesoscopic phase(>15nm) phase coherence in quantum spin fluid
as T0, |<triplet|S+q|collective singlet ground state>|2q
even while the 2-spin correlations in ground state are short-ranged:
<0|SiSj|0>=exp-|i-j|/ where ~7
T=0 quantum coherence limited only by inter-impurity spacing
dephasing at finite T observed
What happens when we insert incorrect bonds?
via Ca substitution for Y which adds holes mainly to oxygens
on chains(DiTusa et al ‘94)
…Ni2+-O2--Ni2+- O 2--Ni2+-O--Ni2+-O2--Ni2+ ...
Subgap bound statesin Ca-doped YBaNiO5
Xu et al, unpublished
G. Xu et al., Science, 289(5478), pp. 419-422, (2000)
Ca-doping induces subgap resonance
incommensurability which does not seem to depend on x
sharper at low x
net spectral weight well in excess(~4 times larger) of spectral
Weight for S=1/2 one might associate with added hole
S=1/2 X S=1/2 X S=1/2
O-
Strong coupling JO-Ni between oxygen & nickel spins
net ferromagnetic(no matter what is sign of JO-Ni )
bond of strength JO-Ni 2
S(Q)=cos2(Q) peaks at 2n, nodes at (2n+1)
-4 -3 -2 -1 0 1 2 3 40
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1
but really JHund>>JNi-Ni
Jhund<<JNi-Ni
dispersionless VB state real S=1 chain
•antiferromagnetism survives on a length scale >lattice spacing•edge states are more extended than single lattice spacing
Therefore-
2
coscosh
2/cos)1()()(
Q
QeQFQS
1/
1 2 3 4 50
5
10
15
202
…interference between left and right hand side of bound state wavefunction produces two incommensurate peaks centered around
for finite(rather than infinitesimal) impurity density, interference effect no longer perfect, and node at
partially relieved
Test: No interference effect when chain is cut rather than FM bond inserted -
Direct observation of effective S=1/2 edge state for chain cut by substitution of
nonmagnetic Mg for magnetic Ni
M. Kenzelmann et al. Physical Review Letters , 90, 087202/1-4, (2003)
Immobile holes in 1-d quantum spin liquid nucleate subgap edge states
Incommensurate structure factor
- not from charge ordering Fermi surface etc.
- but from delocalized quantum spin degree of freedom which extendsover several Ni-Ni spacings into QSF and accounts for large spectral weight
summary
Antiferromagnets in 1d avoid classical order & display mesoscopic quantum effects
1d magnets a good experimental laboratory for edge states in quantum systems