Time resolved ESR study on energy difference of quartet and doublet states in radical-triplet encounter pairs

The energy difference J of quartet and doublet states in a radical-triplet pair (RTP) has been studied in pairs of triplet naphthalene (Np) derivative/galvinoxyl(Galv) and triplet biphenyl (Biph) derivative/Galv systems by time resolved ESR spectroscopy. Most of the systems studied show an unusual positive sign for J that corresponds to the relative location of the quartet state being below the doublet state. In order to explain this unusual sign of J in RTPs, the effects of intermolecular charge transfer (CT) states were examined. The observation was explained by introducing configuration interaction between zero-order RTP (RTP⁰) and CT (CT⁰) states in the encounter pair, where the RTP⁰ state is located above the CT⁰ state. Among the RTP systems examined, triplet 1-chloro-Np/Galv, triplet 1-bromo-Np/Galv and triplet 4-cyano-Biph/Galv systems show a normal negative value of J. On the basis of the estimated energy gap between the RTP⁰ and CT⁰ states, it was concluded that configuration interaction is not significant in these three RTP systems. The value of J in these RTP systems is dominated by exchange interaction, giving a negative sign. The solvent effect on the sign of J in a triplet Np/Galv system is also reported, as evidence that the sign of J is controlled by the CT⁰ state.     

自由基-三重态对化学诱导动态电子极化强度的全哈密顿计算(英文)

基于考虑含E(S2Tξ-S2Tη)项的相互作用全哈密顿,利用密度矩阵运动方程,对自由基-三重态对机理的CIDEP强度进行了详细的理论计算.计算结果表明:四重态母体自由基-三重态机理(QP-RTPM)和二重态母体自由基-三重态机理(DP-RTPM)分别使稳定自由基形成发射+发射/吸收(E+E/A)和吸收+吸收/发射(A+A/E)型多重性极化,其中净E(A)极化由零场分裂相互作用产生,超精细相关E/A(A/E)极化由超精细相互作用产生.另外,零场分裂相互作用项E(S2Tξ-S2Tη),使稳定自由基的净极化减弱     

FT-EPR study on the sign of exchange interaction in triplet naphthalene-galvinoxyl encounter pair

Chemically induced dynamic electron polarization (CIDEP) created in the quenching of triplet naphthalene by galvinoxyl were investigated by time-resolved Fourier-transform electron paramagnetic resonance (FT-EPR) measurements with monitoring a free induction decay signal of a pulsed microwave irradiation. Transient FT-EPR spectra of galvinoxyl with CIDEP were observed in various nonpolar solvents with different viscosity. A transient FT-EPR signal phase shows remarkable dependence on the viscosity: FT-EPR signal phases were absorption and emission in the solvents with low and high viscosity, respectively. Time evolutions of the FT-EPR signal of galvinoxyl were well simulated by a model of the radical-triplet pair mechanism (RTPM) for CIDEP. A sign of theJ value in the triplet naphthalene-galvinoxyl system in various solvents were discussed on the basis of the sign rule in the RTPM and the transient FT-EPR signal phase. One of possible explanation for the solvent viscosity dependence of the transient FT-EPR signal phase was pressented on the basis of hypothetical model of theJ value.     

Theoretical study of the intensity of chemically induce dynamic electron polarization of radical-triplet pairs

Considering the interaction between encited triplet molecule and cloublet radical,based on the second-order perturbation theroy and the motion equation of density matrix,the polarzation intersity of RTPM were theoretically calculated with the overpopulated doublet spin states and quartet spin states of radical0triplet paris as initial conditions the radical result from the zero-field-splitting(zfs)and the multiplet A/E and E/A polarization result from hyperfine (hf) interactions of the triplet molcule,The hyperfine ralated A A/E or E E/A CIDEP on the radical were the overpopulation of the net abscrptive or emissive polarization and multiple A/E or E/A polarization.     

Possible mechanism of charge stripe formation based on the ring exchange interaction

Using the numerical diagonalization of the finite-cluster t–J model, we investigate the mechanism of the charge stripes based on the ring exchange interaction. We calculate the many-hole correlation functions related with the two-types of charge stripes; the vertical and diagonal types of the charge stripe. As a result, we present a phase diagram including the two stripe phases and a phase separation phase.     

Study of deuteron-proton charge exchange reaction at small transfer momentum

The charge exchange reaction at 1 GeV projectile proton energy is studied in the multiple-scattering expansion technique. This reaction is considered in a special kinematics, when the momentum transfer from the beam proton to the fast neutron is close to zero. The differential cross-section and a set of polarization observables are calculated. It was shown that the contribution of the final-state interaction between two protons is very significant.Received: 29 April 2004, Published online: 5 October 2004PACS: 21.45. + v Few-body systems - 13.75.-n Hadron-induced low- and intermediate-energy reactions and scattering (energy 10 GeV) - 25.45.Kk Charge-exchange reactions     

Long-distance quantum state transfer through cavity-assisted interaction

We propose a scheme for long-distance quantum state transfer between different atoms based on cavity-assisted interactions. In our scheme, a coherent optical pulse sequentially interacts with two distant atoms trapped in separated cavities. Through the measurement of the state of the first atom and the homodyne detection of the final output coherent light, the quantum state can be transferred into the second atom with a success probability of unity and a fidelity of unity. In addition, our scheme neither requires the high-Q cavity working in the strong coupling regime nor employs the single-photon quantum channel, which greatly relaxes the experimental requirements.     

Effect of exchange on charge density waves in layered compounds

The first-order (exchange) correction π₁(q) to the static polarizability of an interacting two-dimensional electron gas is calculated numerically, and is found to be sharply peaked at q=2k_F. An estimate of the magnitude of this correction in metallic layered compounds shows that the exchange enhancement of the polarizability is comparable to the band structure enhancement. Exchange and correlation therefore play an important role in the charge density wave instabilities observed in these compounds.     

低电荷态离子原子碰撞过程中的转移电离机理的研究

介绍了使用位置灵敏技术和飞行时间方法研究中低能低电荷态离子-原子碰撞过程中转移电离与单电子俘获过程.对于确定的入射离子电荷态,通过理论分析及与实验数据对比给出了转移电离与单电子俘获截面比R_TS随着入射离子速度V_P的变化规律和转移电离过程中电离的电子主要来自靶原子的最外亚壳层. 关键词： 转移电离 逃离半径 电离半径 俘获半径     

Amplitude analysis of πN charge exchange at large momentum transfer

We have found evidence for the right-signature zero at t ≈ ?1.5 (GeV/c)² and the second wrong-signature zero at t ≈ ?2.5 (GeV/c)² in the helicity flip ?-Regge-pole exchange from an amplitude analysis of πN charge exchange extended to large momentum transfer. Reconstruction of the imaginary part of the nonflip amplitude suggests a remarkable degree of Regge behaviour out to large ?t. Confirmation of such behaviour would undermine the basic features of absorptive cut models.     

Effect of exchange interaction on the spin fluctuations of localized electrons

A microscopic theory of spin fluctuations in an ensemble of electrons localized on donors in a bulk semiconductor has been developed. Both the hyperfine interaction of the electron spin with spins of host lattice nuclei and the exchange interaction between the electrons have been taken into account. A model of clusters to calculate spin noise spectra of the ensemble of localized charge carriers has been proposed. It has been shown that the electron-electron exchange interaction leads to an effective averaging of random nuclear fields and a shift of the peak in the spin-fluctuation spectrum towards lower frequencies.     

Exchange interaction of S state ions with charge carriers in SnTe

ESR investigations of Mn, Eu and Gd in highly degenerate SnTe - a p-type semiconductor with metallic behaviour - prove the existence of an exchange interaction between localized magnetic moments and charge carriers. The ratio of the exchange parameters J_Mn and J_Eu between charge carriers and Mn or Eu ions, respectively, amounts to |J_Mn/J_Eu| = 8 ± 1.5. The consequence this result has on long range spin-spin interaction via charge carriers as well as on hyperfine interaction is discussed.     

Near resonance charge transfer from a laser excited donor state

A laser induced charge transfer from Na(3p) to hydrogen-ions at different kinetic energies has been studied. An enhancement factor of about 90% in the production rate of Lyman-α radiation has been demonstrated to occur only with H⁺ and Na(3p) atoms reaction; no enhancement was observed with either H ₂ ⁺ or H ₃ ⁺ ions. Absolute cross-section for the production of Lyman-α radiation during the collision of H⁺, H ₂ ⁺ and H ₃ ⁺ ions and Na(3p) and Na(3s) atoms have been measured in the energy range 1–600eV. The charge exchange reactions involving hydrogen-ions and Na(3p) atoms created by two different methods have also been compared.     

Effect of vacancy charge state on positron annihilation in silicon

The charge-state-dependent lattice relaxation of mono-vacancy in silicon is studied using the first-principles pseu- dopotential plane-wave method. We observe that the structural relaxation for the first-neighbor atoms of the mono-vacancy is strongly dependent on its charge state. The difference in total electron density between with and without charge states in mono-vacancy and its relevant change due to the localized positron are also examined by means of first-principles simu- lation, demonstrating the strong interplay between positron and electron. Our calculations reveal that the positron lifetime decreases with absolute charge value increasing.     

Long-range repulsive interaction between molecules on a metal surface induced by charge transfer

The adsorption of a molecular electron donor on Au(111) is characterized by the spontaneous formation of a superlattice of monomers spaced several nanometers apart. The coverage-dependent molecular pair distributions obtained from scanning tunneling microscopy data reveal an intermolecular long-range repulsive potential, which decreases as the inverse of the molecular separation. Density functional theory calculations show a charge accumulation in the molecules due to electron donation into the metal. Our results suggest that electrostatic repulsion between molecules persists on the surface of a metal.     

Effect of palladium oxidation state on the kinetics and mechanism of the charge transfer reaction taking place at the Pd/YSZ interface

Electrode polarization and conductivity measurements were carried out at the Pd/YSZ interface and at conditions close to the Pd–PdO thermodynamic equilibrium. The steady-state current–overpotential characteristics were analyzed with a Butler–Volmer type of equation. Both, apparent exchange current density, I_o, and anodic/cathodic charge transfer coefficients (α_a/α_c), were calculated. Based on the experimental results, it was concluded that the charge transfer at the electrode is rate-determining in the case of PdO during anodic operation and Pd during cathodic operation, while in the other case mass transport of adsorbed oxygen species along the electrode/solid electrolyte interface is in competition with the charge transfer process.     

Effect of charge exchange collisions on the static properties of afully collisional ion sheath

The effect of charge exchange collisions on the properties of a fully collisional, static ion sheath is considered. The existing collisional law, which excludes the effect of electrons, is derived from the fluid equations. The effect of electrons are later considered and an approximate power law solution for the potential is obtained. The effect of collisionality on the sheath properties is discussed. The approximate power law solution, derived with the help of fluid equations, is applied to find the ion energy distribution at the electrode     

最近邻弱交换相互作用对spin-1纳米管磁化强度的影响

利用有效场理论研究了纳米管上最近邻原子间弱交换相互作用对Blume-Capel模型磁化强度的影响,得到了系统格点的磁化强度与最近邻弱交换相互作用和晶场强度的关系。结果表明：最近邻弱交换相互作用和晶场强度等诸多因素相互竞争,使系统表现出丰富的磁学特性。正晶场促进系统的磁化强度,而负晶场对其有抑制作用;负晶场作用下,磁化强度基态饱和值小于1,且系统发生一级相变;不同位置的弱交换相互作用对系统的磁化强度影响程度不同。