Charge/orbital ordering structure of Pr(1-x)Ca(x)MnO(3)(x = 3/8) examined by low-temperature transmission electron microscopy

The structural phase transition of Pr(1-x)Ca(x)MnO(3)(x = 3/8) was investigated by means of low-temperature transmission electron microscopy. Superlattice reflection spots with a modulation wave vector q(1) = (0,1/2,0) appeared below 230 K, indicating formation of the d(3x(2-r(2))/d(3y(2)-r(2)) type of charge/orbital ordering. Below 150 K, a new series of superlattice reflection spots with a modulation wave vector q(2) = (1/4,1/4,1/2) appeared, suggesting an additional ordering of excess 1/8 Mn(3+), necessary due to the deviation of x from 1/2, with the occupation of the d(3z(2-r(2)) type of e(g) orbital.     

Charge and spin order on the triangular lattice: NaxCoO2 at x=0.5

The nature of electronic states due to strong correlation and geometric frustration on the triangular lattice is investigated in connection to the unconventional insulating state of NaxCoO2 at x=0.5. We study an extended Hubbard model using a spatially unrestricted Gutzwiller approximation. We find a new class of charge and spin ordered states at x=1/3 and x=0.5 where antiferromagnetic (AFM) frustration is alleviated via weak charge inhomogeneity. At x=0.5, we show that the square root of 3a x 2a off-plane Na dopant order induces weak square root of 3a x 1a charge order in the Co layer. The symmetry breaking enables successive square root of 3a x 1a AFM and 2a x 2a charge- or spin-ordering transitions at low temperatures. The Fermi surface is truncated by the 2a x 2a hexagonal zone boundary into small electron and hole pockets. We study the phase structure and compare to recent experiments.     

双层钙钛矿(La_(1-x)Gd_x)_(4/3)Sr_(5/3)Mn_2O_7(x=0,0.05)的相分离

采用传统固相反应法制备(La1-xGdx)4/3Sr5/3Mn2O7(x=0,0.05)多晶样品,并通过测量样品的磁化强度与温度的变化曲线(M-T曲线)、电子自旋共振谱(ESR谱)和电阻率与温度的变化曲线(ρ-T曲线),研究了x=0和x=0.05样品的相分离现象.研究结果表明,两样品在低温部分出现了反铁磁与铁磁相互竞争的现象,体现出团簇自旋玻璃态的特征.x=0和x=0.05样品分别在125—375 K和100—375 K范围内观察到类Griffiths相,同时发现掺杂使得三维铁磁有序温度(T3Dc0≈125 K和T3Dc1≈100 K)降低,而对类Griffiths温度(TG≈375 K)没有明显影响.在TG温度以上两样品均表现出纯顺磁特性.其电特性表明,x=0样品在整个测量范围内出现两次绝缘-金属转变,这是由钙钛矿锰氧化物共生现象所致.而x=0.05样品只出现一次绝缘-金属转变,表明掺杂能抑制共生现象的产生.通过对ρ-T曲线的拟合发现两样品在高温部分的导电方式基本都遵循三维变程跳跃的导电方式.     

Quantum magnetism in the paratacamite family: towards an ideal kagomé lattice

We report muon spin rotation measurements on the S=1/2 (Cu2+) paratacamite ZnxCu4-x(OH)6Cl2 family. Despite a Weiss temperature of approximately -300 K, the x=1 compound is found to have no transition to a magnetic frozen state down to 50 mK as theoretically expected for the kagomé Heisenberg antiferromagnet. We find that the limit between a dynamical and a partly frozen ground state occurs around x=0.5. For x=1, we discuss the relevance to a singlet picture.     

Magnetic Properties and Spin State Transition of Gallium Doped Perovskite Cobaltite Oxide

A series of Ga doping perovskite cobaltite La2/3Sr1/3 （Co1-y Gay）03 （y = 0, 0.1, 0.2, 0.3 and 0.4） are prepared by the standard solid-state reaction method. Their magnetic properties and Co ions spin state transitions are studied. Upon doping, no appreciable structure changes can be found. However, the corresponding Curie temperature sharply decreases and the magnetization is greatly reduced, indicating that Ga doping destroys the ferromagnetic interaction in the system. In addition, the high temperature magnetization data follow the Curie-Weiss law. At least one kind of Co ions （Co^3＋ or Co^4＋） favours the mixed spin state, and most Co ions are at the lower spin state （low and intermediate state）. With increasing Ga content, more Co ions transit to the higher spin state.     

Muon spin relaxation and susceptibility studies of the pure and diluted spin 1/2 kagomé-like lattice system (CuxZn(1-x))3V2O7(OH2) 2H2O

Muon spin relaxation and magnetic susceptibility measurements have been performed on the pure and diluted spin 1/2 kagomé system (CuxZn(1-x))3V2O7(OH)2 2H2O. In the pure x=1 system we found a slowing down of Cu spin fluctuations with decreasing temperature towards T approximately 1 K, followed by slow and nearly temperature-independent spin fluctuations persisting down to T=50 mK, indicative of quantum fluctuations. No indication of static spin freezing was detected in either of the pure (x=1.0) or diluted samples. The observed magnitude of fluctuating fields indicates that the slow spin fluctuations represent an intrinsic property of kagomé network rather than impurity spins.     

First-Principles Studies for the Electronic Structures of Diluted Magnetic Semiconductors （Ga, Fe）As

First-principles LMTO-ASA band calculations are performed for Ga1-xFezAs (x = 1, 1/4, 1/8) by assuming supercell structures. It is found that the antiferromagnetic (AFM) state is stable for x = 1/4. For x = 1/8, ferromagnetic (FM) state is more stable than AFM state, and no stable magnetic state exists for x = 1. In both the cases the magnetic moments of As and Ga atoms are parallel to those of the nearest Fe atoms due to the p-d hybridization. Fhrther, the band structure shows rather localized Fe 3d state in the gap, and the parallel polarization is confined rather in the vicinity of Fe site.     

Stripes induced by orbital ordering in layered manganites

Spin-charge-orbital ordered structures in doped layered manganites are investigated using an orbital-degenerate double-exchange model tightly coupled to Jahn-Teller distortions. In the ferromagnetic phase, unexpected diagonal stripes at x = 1/m ( m = integer) are observed, as in recent experiments. These stripes are induced by the orbital degree of freedom, which forms a staggered pattern in the background. A pi shift in the orbital order across stripes is identified, analogous to the pi shift in spin order across stripes in cuprates. At x = 1/4 and 1/3, another nonmagnetic phase with diagonal static charge stripes is stabilized at intermediate values of the t(2g)-spins exchange coupling.     

First-Principles Studies for the Electronic Structures of Diluted Magnetic Semiconductors (Ga, Fe)As

First-principles LMTO-ASA band calculations are performed for Ga1-xFexAs (x = 1, 1/4, 1/8) by assuming supercell structures. It is found that the antiferromagnetic (AFM) state is stable for x = 1/4. For x = 1/8, ferromagnetic(FM) state is more stable than AFM state, and no stable magnetic state exists for x = 1. In both the cases the magneticmoments of As and Ga atoms are parallel to those of the nearest Fe atoms due to the p-d hybridization. Further, theband structure shows rather localized Fe 3d state in the gap, and the parallel polarization is confined rather in thevicinity of Fe site.     

On Essential Self-Adjointness for Magnetic Schrödinger and Pauli Operators on the Unit Disc in $${\mathbb {R}^2}$$

We study the question of magnetic confinement of quantum particles on the unit disk \({\mathbb {D}}\) in \({\mathbb {R}^2}\) , i.e. we wish to achieve confinement solely by means of the growth of the magnetic field \({B(\vec x)}\) near the boundary of the disk. In the spinless case, we show that \({B(\vec x)\ge \frac{\sqrt 3}{2}\cdot\frac{1}{(1-r)^2}-\frac{1}{\sqrt 3}\frac{1}{(1-r)^2\ln \frac{1}{1-r}}}\) , for \({|\vec x|}\) close to 1, insures the confinement provided we assume that the non-radially symmetric part of the magnetic field is not very singular near the boundary. Both constants \({\frac{\sqrt 3}{2}}\) and \({-\frac{1}{\sqrt 3}}\) are optimal. This answers, in this context, an open question from Colin de Verdière and Truc (Ann Inst Fourier 2011, Preprint, arXiv:0903.0803v3). We also derive growth conditions for radially symmetric magnetic fields which lead to confinement of spin 1/2 particles.     

Li(AlxCo1-x)O2晶体中Co3+电子态的变化及对结构演化的影响

研究了应用于锂二次电池正极的新型高能量密度存贮材料Li(AlxCo1-x)O2 (x=01—05)的磁性.发现Al3+的掺杂可导致Co3+中d电子自旋态发生变化，即有部分d电子进入高自旋态.伴随Co3+中电子状态的改变，材料结构演化也发生了相应变化，表现为c/a比增大明显减缓，较好地解释了材料结构对Vegard定律的正偏离.这对材料的微观结构与性能设计具有重要意义. 关键词： 锂电池材料 Li（AlxCo1-x）O2 磁性 自旋态 结构演化     

Spin dynamics in the carrier-doped S=1/2 triangular lattice of NaxCoO2.yH2O

We probed the local electronic properties of the mixed-valent Co+4-x triangular lattice in NaxCoO2.yH(2)O by 59Co NMR. We observed two distinct types of Co sites for x > or =1/2, but the valence seems averaged out for x approximately 1/3. Local spin fluctuations exhibit qualitatively the same trend down to approximately 100 K regardless of the carrier concentration x, and hence the nature of the electronic ground state. A canonical Fermi-liquid behavior emerges below approximately 100 K only for x approximately 1/3.     

Antiferromagnetic spin fluctuations above the dome-shaped and full-gap superconducting states of LaFeAsO1-xFx revealed by (75)As-nuclear quadrupole resonance

We report a systematic study by (75)As nuclear-quadrupole resonance in LaFeAsO(1-x)F(x). The antiferromagnetic spin fluctuation found above the magnetic ordering temperature T(N) = 58 K for x = 0.03 persists in the regime 0.04 ≤ x ≤ 0.08, where superconductivity sets in. A dome-shaped x dependence of the superconducting transition temperature T(c) is found, with the highest T(c) = 27 K at x = 0.06, which is realized under significant antiferromagnetic spin fluctuation. With increasing x further, the antiferromagnetic spin fluctuation decreases, and so does T(c). These features resemble closely the cuprates La(2-x)Sr(x)CuO(4). In x = 0.06, the spin-lattice relaxation rate (1/T(1)) below T(c) decreases exponentially down to 0.13T(c), which unambiguously indicates that the energy gaps are fully opened. The temperature variation of 1/T(1) below T(c) is rendered nonexponential for other x by impurity scattering.     

Glassy spin dynamics in non-fermi-liquid UCu5-xPdx, x = 1.0 and 1.5

Local f-electron spin dynamics in the non-Fermi-liquid heavy-fermion alloys UCu5-xPdx, x = 1.0 and 1.5, have been studied using muon spin-lattice relaxation. The sample-averaged asymmetry function G(t) indicates strongly inhomogeneous spin fluctuations and exhibits the scaling G(t,H) = G(t/H(gamma)) expected from glassy dynamics. At 0.05 K gamma(x = 1.0) = 0.35+/-0.1, but gamma(x = 1.5) = 0.7+/-0.1. This is in contrast to inelastic neutron scattering results, which yield gamma = 0.33 for both concentrations. There is no sign of static magnetism approximately greater than 10(-3)(B)/U ion in either material above 0.05 K. Our results strongly suggest that both alloys are quantum spin glasses.     

Ab initio study of the electronic and magnetic properties of Sr(2-x)La(x)Fe(1+y/2)Mo(1-y/2)O6 double perovskites

Using the first-principles full potential linearized augmented plane wave method, the electronic structure of Sr(2-x)La(x)Fe(1+y/2)Mo(1-y/2)O6 (SLFMO) double-perovskite systems is investigated for x = 1/2 and 1 and for y = +1 and -1. Substituting Sr atoms by La atoms allows one to tune the electrons added into the minority spin band and enhances the half-metal feature--according to the rigid band shift model--even if the magnetization decreases with increasing La concentration. By taking into account the chemical disorder on the Fe and Mo sites, resulting from the introduction of La as shown experimentally, it is shown (i) that a supplemental magnetization reduction occurs because the magnetic moment on the Fe antisite is opposite to the one on the Fe regular sites and (ii) that the half-metal feature is preserved in SLFMO for x = 1/2 and 1 contrary to the case for SFMO. Finally, because surface or interface Fe deficiency should have a more limited impact on the spin polarization than for SFMO, SLFMO/SrTiO3 multilayers are investigated in order to confirm this prediction by determining the spin polarization at the interface, which is found to remain high.     

Surface states of cobalt nanoislands on Cu111

The electronic structure of thin Co nanoislands on Cu(111) has been investigated below and above the Fermi level (E(F)) by scanning tunneling spectroscopy at low temperature. Two surface related electronic states are found: a strong localized peak 0.31 eV below E(F) and a mainly unoccupied dispersive state, giving rise to quantum interference patterns of standing electron waves on the Co surface. Ab initio calculations reveal that the electronic states are spin polarized, originating from d3(z(2)-r(2))-minority and sp-majority bands, respectively.     

Disordered states in IPA-Cu(ClxBr1-x)3 induced by bond randomness

The mixtures of two spin-gap compounds IPA-Cu(ClxBr1-x)3 are studied by electron paramagnetic resonance and magnetization processes [M(H)]. From electron paramagnetic resonance spectra, the symmetry of the spin-gap state breaks down, even for x=0.99. From M(H) curves for x=0.95 and 0.92, however, spin gaps survive below mu0Hc1=10+/-1 T, and the M(H) slopes bend at mu0Hc3=40+/-1 T, below the saturation field Hc2. Such a curvature suggests an exotic phase transition: Bose-Einstein condensation of spin triplets occurs at Hc1 相似文献   

Rapid collapse of spin waves in nonuniform phases of the second Landau level

The spin degree of freedom in quantum phases of the second Landau level is probed by resonant light scattering. The long wavelength spin wave, which monitors the degree of spin polarization, is at the Zeeman energy in the fully spin-polarized state at ν = 3. At lower filling factors, the intensity of the Zeeman mode collapses, indicating loss of polarization. A novel continuum of low-lying excitations emerges that dominates near ν = 8/3 and ν = 5/2. Resonant Rayleigh scattering reveals that quantum fluids for ν < 3 break up into robust domain structures. While the state at ν = 5/2 is considered to be fully polarized, these results reveal unprecedented roles for spin degrees of freedom.     

Spin,parity, and nature of the xi(1620) resonance

Using a unitary extension of chiral perturbation theory with a lowest-order s-wave SU(3) chiral Lagrangian we study low-energy meson-baryon scattering in the strangeness S=-2 sector. A scattering-matrix pole is found around 1605 MeV which corresponds to an s-wave Xi resonance with J(P)=1/2(-). We identify this resonance with the Xi(1620) state, quoted by the Particle Data Group with I=1/2 but with unknown spin and parity. The addition of the S=-2 state to the recently computed Lambda(1670), Sigma(1620), and N(1535) states completes the octet of J(P)=1/2(-) resonances dynamically generated in this chiral unitary approach.     

O1s and Mn2p NEXAFS on single-layered La1-xSr1+xMnO4: crystal field effect versus orbital coupling mechanism

O1s and Mn2p near-edge X-ray absorption spectroscopy on La_1-xSr_1+xMnO₄ (0 ≤x ≤0.5) single crystals shows that Sr doping does not only provide holes to the system but also induces a continuous transfer of electrons from out-of-plane d_3z2-r2 to in-plane d_3x2-r2/d_3y2-r2 orbitals. Furthermore, a non-vanishing electron occupation of in-plane d_x2-y2 and out-of-plane d_3z2-r2 orbitals is observed up to relatively high doping contents. These findings demonstrate that the energy difference between all these orbital types has to be very small and manifest that the orbital degree of freedom is determined not just by crystal field effects but also by orbital coupling. Moreover, the doping-dependent transfer of spectral weight observed in the current data identifies La_1-xSr_1+xMnO₄ as a charge-transfer insulator.