Influence of the surface electric field in ion-beam-surface interaction at grazing incidence

We have measured the polarization of light emitted after ion surface scattering at small angle of incidence. The measurements are carried out with H⁺-, H ₂ ⁺ - and He⁺-ions under UHV-conditions with mono- and polycrystalline targets. We explain the typical variation of the polarization as “post collision Stark interaction” (PCSI) in the surface electric field, which can force transitions between nearly degenerate terms. The electric field is composed of two different contributions, a strong but short range surface field which is “seen” by atomsand ions and a long range but weak field due to the image charge which is “seen” to first orderonly by ions. The influence of the electric field on H-Balmer radiation is negligible at typical survival distances r_s≧0.35nm. But in contrast to H-atoms He⁺-ions feel the additional influence of the image field leading to a strong alteration of the polarization of the emitted light. The polarization of the Balmer-radiation stemming from Coulomb exploding H ₂ ⁺ -beams is observed to be modified by the electric field of the “spectator proton”.     

Crystal electric field next to a hydrogen-like interstitial— µ+ in PrNi5

Muon spin rotation measurements of the temperature dependence and the anisotropy of the μ⁺ Knight shift in single crystals of the crystal electric field singlet ground state system PrNi₅ reveal pronounced deviations from a linear scaling of the Knight shift with the bulk magnetic susceptibility atT≤50 K. They are explained by a μ⁺ induced modification of the atomic susceptibility of neighboring Pr³⁺ ions. From the Knight shift anisotropy atT> 50 K it is determined that the implanted μ⁺ occupy a single intersitial site, namely the 6i site (0.5, 0, 0.21±0.02). Using this site information, good model fits to the measured data are obtained assuming a μ⁺ induced perturbation of the crystal electric field at the Pr³⁺ ions next to the μ⁺. Apparently, the presence of the μ⁺ leads to a lowering of the local symmetry, causing a lifting of the degeneracy and a pronounced rearrangement of the low lying crystal electric field levels for these ions.     

Nanofabrication using liquid helium films

We propose here a technique for precision deposition of single atoms or ordered arrays of atoms onto a substrate by first suspending the atoms as ions within a superfluid ⁴He film adhering to the substrate via van der Waals forces. The ions are held within the film by a combination of image forces and an externally applied electric field. Turning off the electric field causes the ions to fall toward the substrate and bond to the substrate surface. If the applied electric field comes from a scanned probe above the film, individual atoms can be deposited with atomic precision. A uniform applied electric field can be used to deposit a crystal of ions onto the substrate.     

GeTe和GeSe 分子在外电场下的特性研究

对Ge原子采用6-311++G^**基函数,Te和Se原子采用SDB-cc-pVTZ基函数,利用密度泛函理论的局域自旋密度近似方法优化得到了GeTe和GeSe分子的稳定构型,并计算了外电场作用下GeTe和GeSe基态分子的平衡核间距、总能量、最高已占据分子轨道能量E_H、最低未占分子轨道能量E_L、能隙、谐振频率和红外谱强度. 在上述计算的基础上利用单激发组态相互作用-局域自旋密度近似方法研究了GeTe和GeSe分子在外电场下的激发特性. 结果表明:随着正向电场强度的增大,分子核间距逐渐增大,分子总能量逐渐降低,谐振频率逐渐减小,红外谱强度则逐渐增大. 在0-2.0569×10¹⁰ V·m^-1的电场范围内,GeTe分子的E_H 均高于GeSe分子的E_H;随着正向电场的增大,GeTe与GeSe的E_H差逐渐变大,GeTe的E_L低于GeSe的E_L,它们的E_L均随正向电场的增大而增大. 无外场时,GeTe分子的能隙比GeSe分子的能隙要小;在外电场反向增大的过程中, GeTe和GeSe的分子能隙始终减小. 外电场的大小和方向对GeTe和GeSe分子的激发能、振子强度及跃迁的波长均有较大影响. 关键词： GeTe GeSe 外电场 激发态     

Experimental measurements and modelling of the structure of the radial electric field in RFX

The experimental determination of the radial electric fieldE _r and the associatedE ×B drift velocity at the edge of RFX is presented and possible mechanisms responsible for its generation are discussed.E _r measurements by means of an array of Langmuir probes and those deduced from Doppler spectroscopy of impurity lines agree fairly well. In particular the rotation velocity of the plasma edge has been determined from the Doppler shift of a C III emission line. The observation of other ions characterised by different radial positions, such as B IV and C V, has allowed an estimate of the velocity shear. Typical values of plasma rotation at the edge are around 10 km/s while the velocity shear is of the order of (10⁵−10⁶)s⁻¹ in the spontaneous layer, a few cm thick, usually observed in standard discharges. Plasma rotation has been artificially modified by both positive and negative edge biasing and the associated increase or decrease of the fluid velocity is well in agreement with the radial electric field change. The modification ofE _r during edge biasing and Pulsed Poloidal Current Drive (PPCD) are also reported and interpreted within a momentum balance model. Analytical and self-consistent Monte Carlo models at the plasma edge suggest that impurities have a relevant role in the generation of the radial electric field, due to their relatively large Larmor radius. Presented at the Workshop on Role of Electric Fields in Plasma Confinement and Exhaust, Budapest, 18–19 June 2000.     

Fe-Hydroxysulphates from Bacterial Fe2+ Oxidation

The perturbed angular correlation method (PAC) was applied to investigate the lattice location of implanted ¹¹¹In probe ions in Hf₂Ni and Zr₂Ni intermetallic compounds. It is concluded that the ¹¹¹In/¹¹¹Cd probe nuclei experiencing the highly asymmetric electric field gradient (EFG) occupy the unique hafnium or zirconium 8(h) sites in the investigated phases. Above room temperature, the EFGs decrease linearly with temperature. The results are compared with that of previous PAC measurements with ¹⁸¹Ta probes.     

IMP AC in-beam and out-of-beam;g-factors and pre-equilibrium effects following ion-implantation

An out-of-beam IMPAC technique has been developed to measure theg-factors of the 2 _l ⁺ states in the neutron-deficient Pt isotopes. The hyperfme field for Pt in Fe in those measurements was close to the field obtained in spin-echo and radioactivity measurements, in contrast with in-beam IMPAC measurements for^194,196,198Pt, where smaller field strengths were observed. These data, and static fields from in-beam IMPAC measurements for other ions in the Pt region, show a correlation with the lifetime of the probe state, consistent with the static field being absent for about 10 ps after the ion has come to rest. New and previously published IMPAC data for₇₆Os,₇₇Ir,₇₈Pt and₇₉Au in Fe hosts, are examined to assess whether such measurements may be sensitive to the thermal spike created at the end of the range of an implanted ion.     

Rare earth substituted YBa2Cu3O x

We present some selected results obtained using rare earth Mössbauer spectroscopy, on YBa₂Cu₃O _x partially and/or totally substituted by Yb³⁺, Er³⁺ or Dy³⁺. We report measurements of the single ion crystal field anisotropy and of the size, direction and ordering temperature of the rare earth sublattice magnetic moments. We use dilute¹⁷⁰Yb³⁺ ions to probe both the Cu(2) derived internal (molecular) fields and the fluctuation frequencies of the short range correlated Cu(2) moments. We monitor these frequencies as the carrier level is changed up towards the threshold needed to stabilise superconductivity.     

Adsorption sites of111In and111mCd on Pd(111) surfaces characterized by the electric field gradient

PAC measurements of the electric field gradient at the nucleus of isolated probe atoms on Pd(111) surfaces lead to the identification of five adsorption sites successively occupied by the parents¹¹¹In and^111mCd during annealing between 80K and 600K. The data are consistent with an estimated activation energy for Pd surface self diffusion of E_a=0.76(8)eV.     

Dependence of negative ion formation on inhomogeneous electric field strength in atmospheric pressure negative corona discharge

The dependence of negative ion formation on the inhomogeneous electric field strength in atmospheric pressure negative corona discharge with point-to-plane electrodes has been described. The distribution of negative ions HO^-, NO_x ^- and CO_x ^- and their abundances on the plane electrode was obtained with a mass spectrometer. The ion distribution on the plane was divided into two regions, the center region on the needle axis and peripheral region occurring the dominant NO_x ^- and CO_x ^- ions and HO^- ion, respectively. The calculated electric field strength in inhomogeneous electric field established on the needle tip surface suggested that the abundant formation of NO_x ^- and CO_x ^- ions and HO^- ion is attributed to the high field strength at the tip apex region over 10⁸ Vm^-1 and the low field strength at the tip peripheral region of the order of 10⁷ Vm^-1, respectively. The formation of HO^-, NO_x ^- and CO_x ^- has been discussed from the standpoint of negative ion evolution based on the thermochemical reaction and the kinetic energy of electron emitted from the needle tip.     

The effect of external electric fields on molecular liquids and induced translational motion

A computer simulation is reported of the enantiomer S CHBrClF subjected in the liquid state to intense external fields of force : i) uniaxial electric field E_Z; ii) circularly polarised field at optical frequencies. The molecular dynamics are quantified in detail at field - on equilibrium in case i) using a range of auto correlation functions. The foremost result of the investigation is that the simple uniaxial field E_Z makes the sample $\text{translate}$ in a well defined direction. The direct effect of E_Z on an isolated molecule of S-CHBrClF is purely rotational, but intramolecular rotation/translation coupling converts this rotation into coherent centre of mass translation. This gives rise to direct, $\text{laboratory frame}$, cross correlations of the type <v(t)$\text{J}$^T(o)> where $\text{v}$ is the molecular centre of mass translational velocity and $\text{J}$^T the transposed molecular angular momentum vector. (The existence of these invalidates the classical theory of the Kerr effect.) The molecular dynamics of the hypothetical chiral ion S-CHBrClF^? are looked at with a view to corroborating the predictions by Baranova et al. concerning their response to electric field treatment. Despite the inherent instability of such an ensemble of like-charged ions the simulation can be used to produce a range of auto and cross-correlation functions with which to characterise the ionic dynamics. The effect of treating the ionic ensemble with a field E_Z is reported briefly in terms of the non-vanishing ensemble averaged centre of mass velocity <v_Z&>;.The induced translation in an electric field may be demonstrated on most liquids using a simple experimental set up. Its importance in optically active systems is such that it may be used to separate a racemic mixture into its enantiomers, the translational motion induced in the one enantiomer is necessarily, by symmetry, opposite to that induced in the other enantiomer. The observation therefore has technological importance. Other applications are discussed.     

The magnetic hyperfine field and the electric field gradient at181Ta impurities in Gd metal

The magnetic hyperfine fieldH _hf and the electric field gradientV _zz at¹⁸¹Ta impurties in metallic Gd were determined by time differential perturbed angular correlation measurements with the 133 keV K-conversion electron 482 keV -cascade of¹⁸¹Ta. The sources for these measurements were prepared by implantation of radioactive¹⁸¹Hf ions into Gd. The results are: |H _hf(TaGd; 77 K)|=285(14)kG, and |V _zz(TaGd; 330 K)|=5.32(15)·10¹⁷V/cm². The value ofH _hf fits well into the systematics for 5d impurities in Gd and indicates a positive core polarisation contribution, which is expected if the conduction electrons of Gd have to a large extent d-character. The electric field gradients of the 5d impurities in Gd are not consistent with a proportionality between the ionic and the electronic contribution.     

外电场下二氧化锆的分子结构及其特性

对O原子采用6-311++G*基组,Zr原子采用aug-cc-pVTZ-PP基组,利用密度泛函(B3P86)方法优化得到了ZrO2分子的稳定构型,并研究了不同外电场(0—0.025 a.u.)作用下ZrO2基态分子键长、能量、电荷分布、偶极矩和能级的变化规律.在优化构型的基础上,利用含时密度泛函(TD-B3P86)方法研究了ZrO2分子在外电场作用下前6个激发态的激发能、跃迁波长和振子强度的激发特性.研究结果表明:随着电场强度的增大,Zr—2O的键长增大,而Zr—3O的键长均匀减少,总能量降低,偶极矩增大;最高占据轨道能量基本保持不变,最低未占据轨道和能隙均减小.电场的增大使得激发能减小,各个激发态跃迁波长均发生不同程度的红移现象,因而,利用外电场可以控制ZrO2的发光光谱范围在可见-红外区域扩展.     

Temperature dependence of the electric quadrupole interaction at scandium impurities in zirconium and hafnium

The PAC probe⁴⁴Sc was employed to study the magnitude and temperature dependence of the electric quadrupole interaction at the site of the transition metal Sc in the hexagonal host lattices Zr and Hf. In Zr ∼ 100% of the probe atoms were situated on regular lattice sites and a quadrupole interaction frequency of υ_Q=7.8(1)MHz was measured at room temperature. For Hf the fraction of the probe atoms on regular lattice sites was smaller and a damping of the interaction pattern (υ_Q=9.3(5)MHz at 293 K) could not be excluded. The temperature dependence of the electric field gradient in both host lattices was found to be weak.     

外场下SnS分子结构及其特性

对S原子采用6-311++G**基组,Sn原子采用SDB-cc-pVTZ基组,利用密度泛函(B3P86)方法对SnS分子进行了基态结构优化,并研究了外场作用下SnS基态分子键长、能量、能级分布、电荷布居分布、谐振频率和红外谱强度的影响规律.然后利用含时密度泛函(TD-B3P86)方法研究了SnS分子在外场下的激发特性.结果表明,在所加的电场范围内(-0.04 a.u.-0.04 a.u.),随着正向电场的增大,分子键长和红外谱强度均是先减小后增大;总能E,SnS基态分子的最高已占据轨道能量EH和谐振频率均是先增大后减小;分子的最低未占空轨道能量EL和能隙Eg均随正向电场的增大而减小.随着正向电场的增大,SnS分子由基态至前9个单重激发态跃迁的波长增大,激发能则减小.     

外电场作用下Si_2O分子的激发特性

主要对2种Si2O分子异构体的激发特性进行研究,由计算结果可知,外电场对Si2O分子的激发能,振子强度,跃迁偶极矩及吸收光谱有着显著的影响.无外电场时三角型Si2O(C2v,1A1)分子在可见光区无吸收谱,外电场作用下其在可见光区(407.18—526.93nm)有比较弱的吸收谱.直线型Si-Si-O(C∞v,3Σ-)分子在有无外电场作用时在蓝光和紫光区均有一定的吸收谱,其中比较难得的是在蓝色光区(478.88—488.59nm)呈现较强的吸收谱.     

Mid-infrared dual-comb spectroscopy with 2.4 μm Cr2+:ZnSe femtosecond lasers

The mid-infrared part of the electromagnetic spectrum is the so-called molecular fingerprint region because gases have tell-tale absorption features associated with molecular rovibrations. This region can be for instance exploited to detect small traces of environmental and toxic vapors in atmospheric and industrial applications. Novel Fourier-transform spectroscopy without moving parts, based on time-domain interferences between two comb sources, can in particular benefit optical diagnostics and precision spectroscopy. To date, high-resolution and -sensitivity proof-of-principle experiments have only been reported in the near-infrared region where frequency-comb oscillators are conveniently available. However, as most of the molecular transitions in this region are due to weak overtone bands, this spectral domain is not ideal for sensitive and rapid detection. Here we present a proof-of-principle experiment of frequency-comb Fourier-transform spectroscopy with two Cr²⁺:ZnSe femtosecond oscillators directly emitting in the 2.4 μm mid-infrared region. The acetylene absorption spectrum in the region of the n₁+n₅¹\nu_{1}+\nu_{5}^{1} band, extending from 2370 to 2525 nm, could be recorded within a 10 μs acquisition time without averaging with 12 GHz resolution.     

Electromechanical-induced antiferroelectricben ferroelectric phase transition in PbLa(Zr,Sn,Ti)O3 ceramic

Antiferroelectric—ferroelectric (AFE—FE) phase transition in ceramic Pb_0.97La_0.02(Zr_0.75Sn_0.136Ti_0.114)O₃ (PLZST) was studied by dielectric spectroscopy as functions of frequency (10²—10⁵ Hz) and pressure (0—500 MPa) under a DC electric field. The hydrostatic pressure-dependent remnant polarization and dielectric constant were measured. The results show that remnant polarization of the metastable rhombohedral ferroelectric PLZST poled ceramic decreases sharply and depoles completely at phase transition under hydrostatic pressure. The dielectric constant undergoes an abrupt jump twice during a load and unload cycle under an electric field. The two abrupt jumps correspond to two phase transitions, FE—AFE and AFE—FE.