Photoinduced magnetism and random magnetic anisotropy in organic-based magnetic semiconductor V(TCNE){x} films, for x approximately 2

The V(TCNE){x}, x approximately 2 is an organic-based amorphous ferrimagnet, whose magnetic behavior is significantly affected in the low field regime by the random magnetic anisotropy. It was determined that this material has thermally reversible persistent change in both magnetization and conductivity driven by the optical excitation. Here, we report results of a ferrimagnetic resonance study of the photoinduced magnetism in V(TCNE){x} film. Upon optical excitation (lambda approximately 457.9 nm), the ferrimagnetic resonance spectra display substantial changes in their linewidths and line shifts, which reflect a substantial increase in the random magnetic anistropy. The results reflect the role of magnetic anisotropy in disordered magnets and suggest a novel mechanism of photoinduced magnetism in V(TCNE){x} induced by the increased structural disorder in the system.     

Bonding, backbonding, and spin-polarized molecular orbitals: basis for magnetism and semiconducting transport in V[TCNE]x approximately 2

X-ray absorption spectroscopy (XAS) and magnetic circular dichroism (MCD) at the V L{2,3} and C and N K edges reveal bonding and backbonding interactions in films of the 400 K magnetic semiconductor V[TCNE]x approximately 2. In V spectra, d{xy}-like orbitals are modeled assuming V2+ in an octahedral ligand field, while d{z{2}} and d{x{2}-y{2}} orbitals involved in strong covalent sigma bonding cannot be modeled by atomic calculations. C and N MCD, and differences in XAS from neutral TCNE molecules, reveal spin-polarized molecular orbitals in V[TCNE]x approximately 2 associated with weaker pi bonding interactions that yield its novel properties.     

X-ray magnetic circular dichroism and resonant photomission of V(TCNE)x hybrid magnets

Thin films of V(TCNE)x were deposited in ultrahigh vacuum using a film growth technique based on in situ chemical vapor deposition of tetracyanoethylene, TCNE, and bis-benzene vanadium, V(C6H6)2. The in situ preparation method enabled, for the first time, experimental analysis of oxygen-free films. X-ray magnetic circular dichroism measurements recorded at the V L(2,3) edge confirmed room temperature magnetic ordering. A combination of conventional photoelectron spectroscopy (PES) and resonant photoemission (RPE) measured at the V L3 edge shows that the highest occupied electronic state is V(3d) derived. The rearrangements of the TCNE- related valence electronic states observed in PES and the evidence of V(3d) and TCNE- pi(pi*) orbital overlap contained in RPE spectra, indicate that strong, covalent type bonding occurs between the vanadium and the TCNE molecules.     

Photoinduced magnetization in the organic-based magnet Mn(TCNE)(x)* y(CH2Cl2)

Photoinduced magnetization in a magnet based on organic species is reported for the first time. Upon optical excitation in the blue region of spectrum, Mn(tetracyanoethylene)(x)*y(CH2Cl2) (x approximately 2, y is approximately 0.8) exhibits increased magnetic susceptibility at temperatures as high as 75 K, accompanied with photoinduced absorption in the visible and infrared spectral regions. These effects are partially reversible by lower energy visible light and fully reversible by thermal treatment. The results suggest trapping of the photoexcited charge in a metastable state with enhanced exchange interaction.     

Electrical spin injection from an organic-based ferrimagnet in a hybrid organic-inorganic heterostructure

We report the successful extraction of spin-polarized current from the organic-based room temperature ferrimagnetic semiconductor V[TCNE](x) (x～2, TCNE: tetracyanoethylene; T(C)～400 K, E(G)～0.5 eV, σ(300?K)～10(-2) S/cm) and its subsequent injection into a GaAs/AlGaAs light-emitting diode. The spin current tracks the magnetization of V[TCNE](x～2), is weakly temperature dependent, and exhibits heavy-hole-light-hole asymmetry. This result has implications for room temperature spintronics and the use of inorganic materials to probe spin physics in organic and molecular systems.     

Field-dependent anisotropy change in a supramolecular Mn(II)- [3 x 3] grid

The magnetic anisotropy of a novel Mn(II)- [3x3] grid complex was investigated by means of high-field torque magnetometry. Torque vs field curves at low temperatures demonstrates a ground state with S>0 and exhibits a torque step due to a field-induced level crossing at B(*) approximately 7.5 T, accompanied by an abrupt change of magnetic anisotropy from easy-axis to hard-axis types. These observations are discussed in terms of a spin Hamiltonian formalism.     

Nanomagnetic droplets and implications to orbital ordering in LA(1-x)Sr(x)CoO3

Inelastic cold-neutron scattering on LaCoO3 provided evidence for a distinct low energy excitation at 0.6 meV coincident with the thermally induced magnetic transition. Coexisting strong ferromagnetic (FM) and weaker antiferromagnetic correlations that are dynamic follow the activation to the excited state, identified as the intermediate S = 1 spin triplet. This is indicative of dynamical orbital ordering favoring the observed magnetic interactions. With hole doping as in La(1-x)Sr(x)CoO3 , the FM correlations between Co spins become static and isotropically distributed due to the formation of FM droplets. The correlation length and condensation temperature of these droplets increase rapidly with metallicity due to the double exchange mechanism.     

Electronic structure of thin film iron-tetracyanoethylene: Fe(TCNE)<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>

Thin film iron-tetracyanoethylene Fe(TCNE) _x , x∼2, as determined by photoelectron spectroscopy, was grown in situ under ultra-high vacuum conditions using a recently developed physical vapor deposition-based technique for fabrication of oxygen- and precursor-free organic-based molecular magnets. Photoelectron spectroscopy results show no spurious trace elements in the films, and the iron is of Fe²⁺ valency. The highest occupied molecular orbital of Fe(TCNE) _x is located at ∼1.7 eV vs. Fermi level and is derived mainly from the TCNE⁻ singly occupied molecular orbital according to photoelectron spectroscopy and resonant photoelectron spectroscopy results. The Fe(3d)-derived states appear at higher binding energy, ∼4.5 eV, which is in contrast to V(TCNE)₂ where the highest occupied molecular orbital is mainly derived from V(3d) states. Fitting ligand field multiplet and charge transfer multiplet calculations to the Fe L-edge near edge X-ray absorption fine structure spectrum yields a high-spin Fe²⁺ (3d⁶) configuration with a crystal field parameter 10Dq∼0.6 eV for the Fe(TCNE) _x system. We propose that the significantly weaker Fe-TCNE ligand interaction as compared to the room temperature magnet V(TCNE)₂ (10Dq∼2.3 eV) is a strongly contributing factor to the substantially lower magnetic ordering temperature (T _C ) seen for Fe(TCNE) _x -type magnets.     

Magnetic excitations in EuCu(2)(Si(x)Ge(1-x))(2): from mixed valence towards magnetism

We report the inelastic neutron scattering study of spin dynamics in EuCu(2)(Si(x)Ge(1-x))(2) (x?=?1, 0.9, 0.75, 0.6), performed in a wide temperature range. At x?=?1 the magnetic excitation spectrum was found to be represented by the double-peak structure well below the energy range of the Eu(3+) spin-orbit (SO) excitation (7)F(0)→(7)F(1), so that at least the high-energy spectral component can be assigned to the renormalized SO transition. Change of the Eu valence towards 2?+ with increased temperature and/or Ge concentration results in further renormalization (lowering the energy) and gradual suppression of both inelastic peaks in the spectrum, along with developing sizeable quasielastic signal. The origin of the spectral structure and its evolution is discussed in terms of excitonic model for the mixed valence state.     

Dy3+掺杂Sr1-xCaxMoO4的制备及发光性能研究

采用高温固栩法制备了Dy<'3+>掺杂的Sr1-xCaxMoO<,4>荧光粉.利用XRD、SEM、激发发射光谱以及色参数等研究了所制备荧光粉的结构和发光性能以及x值埘荧光粉性能的影响.XRD图像农明当x=1和x=0时样品为CaMoO<,4>和SrMoO<,4>单一相.SEM 图像表明在750℃下煅烧3 h制备的样品粒径为0.2～1.0μm,适合同态发光器件的要求.监测576 nm得到的样品的激发光谱由250～340 nm之间的一个宽带和340～460 nm之间的一系列尖峰组成.改变Sr/Ca的值,电荷迁移带激发峰位置发生变化,而窄带跃迁的激发峰强度发生变化.用350 nm波长激发样品得到的发射谱由峰值位于480和576 nm的两个窄带组成,它们是由和跃迁引起的.黄色发射峰和监色发射峰的强度比Y/B随着Sr/Ca比值的变化而变化.     

Evolution from a non-Fermi liquid Kondo lattice to intermediate valence behaviour in CeRhSn(1-x)In(x)

We present investigations of the magnetic and electric transport properties, specific heat, and electronic structure of the intermetallic and strongly correlated system of CeRhSn(1-x)In(x) compounds. The main goal of this paper is to determine the hybridization energy between the f electron and conduction electron states, V(cf), and its influence on the ground state properties of the system. The complementary experimental data are discussed on the basis of the Anderson model for a periodic Kondo lattice. CeRhSn is known as a non-Fermi liquid, while CeRhIn is a valence fluctuating system. We discuss the ground state properties of CeRhSn(1-x)In(x) and compare the results with those obtained for the doped Ce-based Kondo insulators.     

顺磁性物质中法拉第磁光效应及其温度特性的量子理论

在某些顺磁性物质中,包括交换作用和外磁场在内的有效场H_i可导致基态能级的分裂。在温度T高于居里点T_c范围内,基态分裂的两个能级上均可存在一定的电子几率分布,从而可导致基态双能级跃迁。根据这一理论进行的计算表明,顺磁性物质的法拉第效应存在多种温度特性。在外磁场不太大的情况下,有些物质的费尔德常数V与磁化率X的比值V/X=A(1+BT);有些物质中V/X=A(1+B/T)。计算还表明,法拉第旋转的实部θ′和虚部θ″均与有效场H_i成正比,并在非吸 关键词：     

Critical point and the nature of the pseudogap of single-layered copper-oxide Bi2Sr2-xLaxCuO6+delta superconductors

We apply strong magnetic fields of H=28.5 to 43 T to suppress superconductivity (SC) in the cuprates Bi2Sr2-xLaxCuO6+delta (x=0.65, 0.40, 0.25, 0.15, and 0), and investigate the low temperature (T) normal state by 63Cu nuclear spin-lattice relaxation rate (1/T1) measurements. We find that the pseudogap (PG) phase persists deep inside the overdoped region but terminates at x approximately 0.05, which corresponds to the hole doping concentration of approximately 0.21. Beyond this critical point, the normal state is a Fermi liquid that persists as the ground state when superconductivity is removed by the magnetic field. A comparison of the superconducting state with the H-induced normal state in the x=0.40 (Tc=32 K) sample indicates that there remains substantial part of the Fermi surface even in the fully developed PG state, which suggests that the PG and SC are coexisting matters.     

Relation between the superconducting gap energy and the two-magnon raman peak energy in Bi(2)Sr(2)Ca(1-x)Y(x)Cu(2)O(8+delta)

The relation between the electronic excitation and the magnetic excitation for the superconductivity in Bi(2)Sr(2)Ca(1-x)Y(x)Cu(2)O(8+delta) was investigated by wide-energy Raman spectroscopy. In the underdoping region the B(1g) scattering intensity is depleted below the two-magnon peak energy due to the charge-spin interactions. The depleted region decreases according to the decrease of the two-magnon peak energy, as the carrier concentration increases. This two-magnon peak energy also determines the B(1g) superconducting gap energy as 2Delta approximately alphaPlanck's over 2piomega(two-magnon) approximately J(eff) (alpha = 0.34-0.41) from under to overdoping hole concentration.     

Magnetic field effect on the static antiferromagnetism of the electron-doped superconductor Pr1-xLaCexCuO4 (x=0.11 and 0.15)

Effects of magnetic fields (applied along the c axis) on static spin correlation were studied for the electron-doped superconductors Pr1-xLaCexCuO4 with x=0.11 (T(c)=25 K) and x=0.15 (T(c)=16 K) by neutron-scattering measurements. In the x=0.11 sample, which is located near the antiferromagnetic (AF) and superconducting phase boundary, a commensurate magnetic order develops below around T(c) at zero field. Upon applying a magnetic field up to 9 T both the magnetic intensity and the onset temperature of the order increase with the maximum field effect at approximately 5 T. In contrast, in the overdoped x=0.15 sample any static AF order is neither observed at zero field nor induced by the field up to 8.5 T. Difference and similarity of the field effect between the hole- and electron-doped high-T(c) cuprates are discussed.     

Possible quantum critical point in La(2/3)Ca(1/3)Mn(1-x)Ga x O3

We study the magnetic ground state in La(2/3)Ca(1/3)Mn(1-x)Ga x O3 manganites, where a quantum critical point (QCP) has been theoretically predicted. The metallic ferromagnetic ground state for low Ga doping breaks down for x > or = 0.11, an insulating state being established at low temperatures. Long-range ferromagnetism coexists with short-range magnetic correlations in the concentration range 0.11 < or = x < or = 0.145 while only the short-range correlations survive for x > or = 0.16. We discuss the implications of such a QCP to the physics of manganites and compare to other QCP systems.     

Thin films of molecule-based charge transfer complex cobalt tetracyanoethylene: In situ X-ray photoemission study

Thin films of molecule-based charge transfer magnet, cobalt tetracyanoethylene [Co(TCNE)_x, x ~ 2] consisting of the transition metal Co, and an organic molecule viz. tetracyanoethylene (TCNE) have been deposited by using physical vapor deposition method under ultra-high vacuum conditions at room temperature. X-ray photoelectron spectroscopy (XPS) technique has been used extensively to investigate the electronic properties of the Co(TCNE)_x thin films. The XPS measurements show that the prepared Co(TCNE)_x films are clean, and oxygen free. The stoichiometries of the films, based on atomic sensitive factors, are obtained, and yields a ~ 1:2 ratio between metal Co and TCNE for all films. Interestingly, the positive shift of binding energy position for Co(2p), and negative shifts for C(1s) and N(1s) peaks suggest a charge-transfer from Co to TCNE, and cobalt is assigned to its Co(II) valence state. In the valence band investigation, the highest occupied molecular orbital (HOMO) of Co(TCNE)_x is found to be at ~ 2.4 eV with respect to the Fermi level, and it is derived either from the TCNE^? singly occupied molecular orbital (SOMO) or Co(3d) states. The peaks located at ~ 6.8 eV and ~ 8.8 eV are due to TCNE derived electronic states. The obtained core level and valence band results of Co(TCNE)_x, films are compared with those of V(TCNE)_x thin film magnet: a well known system of M(TCNE)_x type of organic magnet, and important points regarding their electronic properties have been brought out.     

Magnetic properties of (ErxY1−x)Al2: Magnetic measurements and neutron diffractions data

The ac susceptibility, the low field magnetization and neutron diffraction experiment have been performed for concentrations 0.1<x<1. For x<0.4 the typical spinglass properties have been observed: cusp in the susceptibility, the cusp is affected by small static magnetic fields of a few hundred Gauss. The thermal remanent magnetization has also been detected. However properties are also present for the high concentration x=0.6 or 0.8. Neutron diffraction experiments at the D1B of the ILL show that there exists $\text{no}$ sharp change from long range order to the spinglass regime. For higher x values approximately 80% of the Er ions form long range order whereas for x<40% most of the ions are in the frozen paramagnetic state. The magnetic phase diagram for the whole concentration range is discussed.     

Magnetic properties of multiferroics-semiconductors Eu(1-x)Ce(x)Mn2O5

Studies of magnetization, magnetoresistance, and magnetic oscillations in semiconductor-multiferroics Eu(1-x)Ce(x)Mn2O5 (x = 0.2-0.25) (ECMO) at temperatures ranging from 5 to 350 K in magnetic fields up to 6 T are presented. It is shown that phase separation and charge carrier self-organization in the crystals give rise to a layered superstructure perpendicular to the c axis. An effect of magnetic field cycling on the superstructure, magnetization, and magnetoresistance is demonstrated. X-ray diffraction studies of ECMO demonstrating the effect of magnetic field on the superstructure are presented. The de Haas-van Alphen magnetization oscillations in high magnetic fields and the temperature-induced magnetic oscillations in a fixed magnetic field are observed at low temperatures. Below 10 K the quantum corrections to magnetization due to the weak charge carrier localization in 2D superlattice layers occur. It is shown that at all the temperatures the Eu(1-x)Ce(x)Mn2O5 magnetic state is dictated by superparamagnetism of isolated ferromagnetic domains.     

23Na NMR evidence for charge order and anomalous magnetism in NaxCoO2

Oriented powder samples of NaxCoO2 are studied by 23Na NMR and SQUID magnetometry. In nominal 0.50相似文献