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Register a new userAnderson localization of spinons in a spin-1/2 antiferromagnetic Heisenberg chain
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Anderson localization is a general phenomenon of wave physics, which stems from the interference between multiple scattering paths1,2. It was originally proposed for electrons in a crystal, but later was also observed for light3-5, microwaves6, ultrasound7,8, and ultracold atoms9-12. Actually, in a crystal, besides electrons there may exist other quasiparticles such as magnons and spinons. However the search for Anderson localization of these magnetic excitations is rare so far. Here we report the first observation of spinon localization in copper benzoate, an ideal compound of spin-1/2 antiferromagnetic Heisenberg chain, by ultra-low-temperature specific heat and thermal conductivity measurements. We find that while the spinon specific heat Cs displays linear temperature dependence down to 50 mK, the spinons thermal conductivity ks only manifests the linear temperature dependence down to 300 mK. Below 300 mK, ks/T decreases rapidly and vanishes at about 100 mK, which is a clear evidence for Anderson localization. Our finding opens a new window for studying such a fundamental phenomenon in condensed matter physics.
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Inelastic neutron scattering was used to measure the magnetic field dependence of spin excitations in the antiferromagnetic S=1/2 chain CuCl_2 2(dimethylsulfoxide) (CDC) in the presence of uniform and staggered fields. Dispersive bound states emerge from a zero-field two-spinon continuum with different finite energy minima at wave numbers q=pi and q_i approx pi (1-2<S_z>). The ratios of the field dependent excitation energies are in excellent agreement with predictions for breather and soliton solutions to the quantum sine-Gordon model, the proposed low-energy theory for S=1/2 chains in a staggered field. The data are also consistent with the predicted soliton and n=1,2 breather polarizations and scattering cross sections.
We successfully synthesized the zinc-verdazyl complex [Zn(hfac)$_2$]$cdot$($o$-Py-V) [hfac = 1,1,1,5,5,5-hexafluoroacetylacetonate; $o$-Py-V = 3-(2-pyridyl)-1,5-diphenylverdazyl], which is an ideal model compound with an $S$ = 1/2 ferromagnetic-antiferromagnetic alternating Heisenberg chain (F-AF AHC). $Ab$ $initio$ molecular orbital (MO) calculations indicate that two dominant interactions $J_{rm{F}}$ and $J_{rm{AF}}$ form the $S=1/2$ F-AF AHC in this compound. The magnetic susceptibility and magnetic specific heat of the compound exhibit thermally activated behavior below approximately 1 K. Furthermore, its magnetization curve is observed up to the saturation field and directly indicates a zero-field excitation gap of 0.5 T. These experimental results provide evidence for the existence of a Haldane gap. We successfully explain the results in terms of the $S=1/2$ F-AF AHC through quantum Monte Carlo calculations with $|J_{rm{AF}}/J_{rm{F}}|$ = 0.22. The $ab$ $initio$ MO calculations also indicate a weak AF interchain interaction $J$ and that the coupled F-AF AHCs form a honeycomb lattice. The $J$ dependence of the Haldane gap is calculated, and the actual value of $J$ is determined to be less than 0.01$|J_{rm{F}}|$.
We report zero and longitudinal magnetic field muon spin relaxation measurements of the spin S=1/2 antiferromagnetic Heisenberg chain material SrCuO2. We find that in a weak applied magnetic field B the spin-lattice relaxation rate follows a power law B^n with n=-0.9(3). This result is temperature independent for 5K < T < 300 K. Within conformal field theory and using the Muller ansatz we conclude ballistic spin transport in SrCuO2.
We have investigated the thermal conductivity kappa_mag of high-purity single crystals of the spin chain compound Sr2CuO3 which is considered an excellent realization of the one-dimensional spin-1/2 antiferromagnetic Heisenberg model. We find that the spinon heat conductivity kappa_mag is strongly enhanced as compared to previous results obtained on samples with lower chemical purity. The analysis of kappa_mag allows to compute the spinon mean free path l_mag as a function of temperature. At low-temperature we find l_magsim0.5mum, corresponding to more than 1200 chain unit cells. Upon increasing the temperature, the mean free path decreases strongly and approaches an exponential decay ~1/T*exp(T*/T) which is characteristic for umklapp processes with the energy scale k_B T*. Based on Matthiesens rule we decompose l_mag into a temperature-independent spinon-defect scattering length l0 and a temperature dependent spinon-phonon scattering length l_sp(T). By comparing l_mag(T) of Sr2CuO3 with that of SrCuO2, we show that the spin-phonon interaction, as expressed by l_sp is practically the same in both systems. The comparison of the empirically derived l_sp with model calculations for the spin-phonon interaction of the one-dimensional spin-1/2 XY model yields reasonable agreement with the experimental data.
We study the spectrum and the nature of the excitations of an antiferromagnetic (AFM) Heisenberg chain with staggered long range interactions, both numerically using the time-dependent density matrix renormalization group (tDMRG) method and by means of a multi-spinon approximation that qualitatively explains its main features. The unfrustrated long-range nature of the exchange effectively increases the dimensionality of the system and the chain is able to undergo true symmetry breaking and develop long range order, transitioning from a gapless spin liquid to a gapless ordered AFM phase. We calculated the momentum resolved spin dynamical structure factor and found that for weakly decaying interactions the emergence of Neel order can be associated to the formation of bound states of spinons that become coherent magnons. The quasiparticle band leaks out from the two-spinon continuum that is pushed up to higher energies. Our physical picture is also supported by an analysis of the behavior of the excitations in real-time.
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