极性分子摆动态的三体量子关联

极性分子具有较长的相干时间和较强的偶极-偶极相互作用,因此它被视为量子信息处理的有效量子载体.基于分子摆动态作为量子比特,研究了处于热平衡状态下三极性分子线性链系统的三体量子关联特性,分析了三体负性熵纠缠度、测量诱导扰动和三体量子失协随与电场强度、分子电偶极矩、分子转动常数、偶极-偶极相互作用和温度等参数有关的三个无量纲变量之间的变化关系.研究表明:在其他参数给定的情况下,随电场强度的增加,三体量子关联均变小;随偶极-偶极相互作用强度的增大,三体量子关联先增加到峰值再逐渐变小;温度越高,负性熵纠缠度和三体量子失协越小,但测量诱导扰动随温度的改变在电场强度和偶极-偶极相互作用影响下呈现不同的变化趋势.此外,通过调节电场强度、偶极-偶极相互作用和温度,可改变与操控极性分子摆动态的三体量子关联.     

Narrow states in38,40Ar via alpha +34,36S scattering

Excitation functions of the elastic scattering α+ ^34,36 S has been measured at beam energies E _α =12.56–15.00 MeV. Strongly fluctuating large cross sections in backward angles have been observed. Angular distributions were measured in the range θ _lab =98°–173° for fourteen energies, and many of them turned out to be dominated by one exclusive angular-momentum value, a behaviour typical for resonance scattering.     

Reactive scattering of a supersonic oxygen atom beam O+ICl

Reactive scattering of O atoms with ICl molecules has been studied at an initial translational energy E = 40 kJ mol^-1 using a supersonic beam of O atoms seeded in He and at E = 15 kJ mol^-1 using O atoms seeded in Ne. Velocity distributions of OI product were measured by cross-correlation time-of-flight analysis. Full contour maps of the differential reaction cross-section have been obtained which show peaking almost equally in the forward and backward directions at both initial translational energies. The product translational energy distributions are consistent with a long-lived O-I-Cl collision complex dissociating via a loose transition state. The stability of the O-I-Cl complex is attributed to the low electronegativity of the central I atom compared with the peripheral atoms. This electronegativity ordering rule also determines the stability of the intermediates in the other reactions of oxygen atoms with halogen molecules. The mild peaking of the product angular distributions for O + ICl and IBr indicates that collision complexes have quite modest collision angular momenta L ～ 40 ? corresponding to impact parameters b ～ 1·4 Å and that the angular momentum of the OI molecule in the loose transition state may be approximately half the product orbital angular momentum.     

Inelastic electron scattering from low-lying states in the nuclei 36Ar and 40Ar

The low-lying level structure of ³⁶Ar and ⁴⁰Ar has been investigated using the technique of inelastic electron scattering. Data were collected at the National Bureau of Standards Linear Accelerator with incident electron energies between 65 and 115 MeV and scattering angles of 92.5° and 110°. The data span a range of momentum transfer squared between 0.29 and 0.92 fm^?2. Tassie model and Helm model analyses have been applied to data for levels at 1.97 and 4.18 MeV in ³⁶Ar and at 1.46, 2.52, 3.21 and 3.68 MeV in ⁴⁰Ar. A 2⁺ assignment to the 3.21 MeV state in ⁴⁰Ar is suggested. Transition strengths, transition radii, and mean lifetimes for these states are computed and compared with results of previous experiments.     

Polarization spectroscopy of ion-pair states of ICl

Molecular constants for the E0⁺(³P₂) and 1(³P₂) ion-pair states of ICl vapor have been determined using sequential two-photon polarization-labeling spectroscopy. The two states are coupled by a heterogeneous perturbation which is analyzed in some detail for low-lying vibrational levels of 1(³P₂). The I³⁵Cl potential constants for the 1(³P₂) state and the rotation-vibration constants for the set of f sublevels—i.e., the constants unaffected by coupling with the E state—are (in cm⁻¹) 1(³P₂): Y_0,0= 39103.814(32), Y_1,0= 170.213(15), Y_2,0= −0.4528(22), Y_3,0= −7.0(12) × 10⁻⁴, Y_4,0= −1.48(24) × 10⁻⁵ and Y_5,0= −6.6(19) × 10⁻⁸, Y^(f)_0,1= 5.6878(17) × 10⁻² Y^(f)_1,1= −2.110(24) × 10⁻⁴, Y^(f)_2,1= −1.23(62) × 10⁻⁷, and Y^(f)_0,1= −3.08(22) × 10⁻⁸Likewise, the I³⁵Cl constants determined for the E 0⁺(³P₂) state are E 0⁺(³P₂: Y_0,0= 39054.38(61), Y_1,0= 166.96(10), Y_2,0 = −0.3995(42), Y_0,1= 5.738(31) × 10⁻², and Y_1,1= −1.67(26) × 10⁻⁴Practical constraints in pumping the sequence E 0⁺ ← B 0⁺ ← × 0⁺ restrict the analysis of the E state to levels v = 9–15. Given the long extrapolation to the equilibrium state the 3σ statistical uncertainties quoted for these constants should be treated with caution.     

Reactive scattering of oxygen atoms: O+I2, ICl,Br2

Angular and velocity distribution measurements of IO reactive scattering from crossed beams of O atoms and halogen molecules I₂, ICl are reported. Angular distribution measurements are reported for BrO from O + Br₂. The O atom beam was generated at ～350 K from a microwave discharge source and the halogen molecule beam from a supersonic nozzle source at ～380 K. The product time-of-flight distribution was recorded at each laboratory scattering angle by a mini-computer. The scattering data are found to be in excellent agreement with the RRKM-AM model of reactive scattering via a long-lived collision complex. The observation of IO product from O + ICl identifies the complex with a bound O-I-Cl triplet state, previously observed for O-Cl-Cl in matrix isolation studies, as proposed by Herschbach. The maximum centrifugal barrier B _m′ for dissociation of the long-lived complex can be accurately determined, particularly for O + I₂. The B _m′ values indicate that both the entrance and exit valleys of the potential energy surface are governed by centrifugal barriers in the region of long-range van der Waals potentials. The comparatively small reaction cross section (e.g. Q ～ 2 Ų for O + Br₂ from discharge flow measurements) is attributed primarily to an orientation requirement for reaction. The RRKM-AM model indicates a ‘tight linear’ transition state for dissociation of the O-I-I complex, corresponding to significant long-range IO orienting forces in the exit valley of the potential energy surface.     

Accurate Ne−H+ and Ar−H+ interactions from spectroscopic and scattering states: A comparison of theory with experiments

Summary The groud-state interaction potentials for the Ne(¹S) and Ar(¹S) systems with H⁺ as a partner have been obtained in a rather simple analytic form and with a parameter optimization that took into consideration a broad range of experimental data, thus extending and verifying earlier work which considered only scattering experiments. It is clearly shown by the present work that the available spectroscopic data on the location of the diatomic bound states and on the transitions between them, the measured differential cross-sections at various collision energies and the mobility coefficients at variousE/N values are all well reproduced by our final potential forms, as apposed to the poorer performances of earlier analytic potential forms, as apposed to the poorer performances of earlier analytic potentials that had been suggested for the same systems. As a consequence of the present analysis very accurate, multiproperty potential functions are thus obtained and provided for the two systems under study. To speed up publication, the authors of this paper have agreed to not receive the proofs for correction.     

Photostop of iodine atoms from electrically oriented ICl molecules

The dynamics of photostopping iodine atoms from electrically oriented ICl molecules was numerically studied based on their orientational probability distribution functions. Velocity distributions of the iodine atoms and their production rates were investigated for orienting electrical fields of various intensities. For the ICl precursor beams with an initial rotational temperature of~1 K, the production of the iodine atoms near zero speed will be improved by about~5 times when an orienting electrical field of~200 k V/cm is present. A production rate of~0.5‰ is obtained for photostopped iodine atoms with speeds less than 10 m/s, which are suitable for magnetic trapping. The electrical orientation of ICl precursors and magnetic trapping of photostopped iodine atoms in situ can be conveniently realized with a pair of charged ring magnets. With the maximal value of the trapping field being~0.28 T, the largest trapping speed is~7.0 m/s for the iodine atom.     

气体-表面相互作用的分子动力学模拟研究

采用分子动力学模拟方法研究了气体分子Ar在光滑和粗糙Pt表面上的散射规律.提出了一种速度抽样方法,计算了不同温度条件下气体分子对光滑和粗糙表面的切向动量适应系数和吸附概率.结果显示：光滑表面条件下,气体分子的切向动量系数和吸附概率都随着温度的升高而降低;粗糙度对气体分子切向动量与表面的适应具有极大的促进作用,当粗糙度足够大时,切向动量适应系数的大小趋近于1.0,对温度的敏感性也逐渐降低.采用粒子束方法对气体分子在光滑和粗糙表面上的散射规律进行了定量分析.总结了散射过程中气体分子的典型轨迹和动量变化规律,将气体分子在光滑表面的散射分为两种类型：单次碰撞后散射和多次碰撞后散射.单次碰撞后散射的气体分子平均切向动量有所减小,而经过多次碰撞后散射的气体分子则倾向于保持原有的平均切向动量.对于粗糙表面,粗糙度的存在使气体分子与表面间的动量和能量适应更加充分,导致气体分子在较粗糙表面上散射后的平均切向动量大幅减小并接近于0,且气体分子在表面上经历的碰撞次数越多,其散射后的能量损失越严重.     

Polarization spectroscopy of ICl: The D′, a and a′ states

Three previously-unanalyzed states of ICl are reported, an ion-pair state D′(Ω =2) which converges to the limit I⁺(P₂+ Cl^-(S_o), and two shallow states a(Ω = 1) and a′(Ω = 0⁺) both of which converge to the ground states of separated atoms I(P_{$\text{3}\text{2}$}) + Cl(P_{$\text{3}\text{2}$}). The a(0⁺) state is responsible for the well-known interruption of the B(0⁺) state above υ_B = 3. Spectroscopic constants are given for the D′ and a′ states.     

High-spin states in38Ar

Theγ-decay of 93³⁸Ar levels between 6.84 and 10 MeV excitation energy has been measured using the³⁵Cl(α,pγ) reaction atE _α=14 MeV. A previous measurement of the same reaction could be exploited in the light of the present results, yielding spin(-parity) assignmentsJ ^π(7,070)=5^-, J(7,507)=7,5,J ^π(8,077)=7⁺, J(8,129)=5,6 and J(8,488)=7,5. Theγ-decay modes of yrast levels, which have been previously observed in heavy ion induced reactions, are revised leading to major changes in their spin-parity assignments. New candidates for theJ ^π=8^- and 9⁺ levels were found in the levels at 9,644 and 9,928 keV excitation energy, respectively. A comparison of yrast levels with shell-model calculations is satisfying.     

Observation of transitions involving core-excited states in Ar III and Ar IV and high-lying singly excited states in Ar I–Ar IV

In this paper we present a comprehensive analysis of beam-foil and beam-gas excited spectrum of argon observed in small wavelength region, 2965–3090 Å, using Ar^+/2+ ions in the energy range 200–650 keV. The comparison of beam-foil spectrum (BFS) at different incident beam energy and with that of beam-gas spectrum (BGS), one can find solution for blending problem in beam-foil spectroscopy. Many new transitions were identified on the basis of calculated wavelength from the accurately known energy levels of Ar I, Ar II, Ar III and Ar V. The transitions of Ar I originate from highly excited states (10p to 17p and 10f to 17f). Based on TOPbase estimates using close-coupling approximation five transitions involving core-excited states and nine transitions originating from highly excited states in the spectrum of Ar III and Ar IV were also identified. Radiative life time of two core excited quintet states (3s3p⁴(⁴P)6d ⁵D and 3s3p⁴(⁴P)8f⁵F^o) of Ar III were measured and found to be in ‘good’ agreement with that of the calculated value using close-coupling approximation.     

Probing electronic states of Ne2+ and Ar2+ by measuring kinetic-energy-release distributions

Dissociative decay of metastable, electronically excited neon and argon dimer ions produces fragment ions with strikingly dissimilar kinetic-energy-release distributions. The distributions have been modeled based on ab initio calculations of potential energy curves. The unusual bimodal distribution observed for dissociation of Ne2+ arises from competition between radiative and nonradiative decay of the long-lived II(1/2)(u) state. For Ar2+, however, electronic predissociation is insignificant.     

Measurement of the lifetime of the3 P 2 and4 P 5/2 states in Ar16+ and Ar15+

Promptly decaying levels in Li- and Be-like Ar could be identified in the delayed x-ray and electron spectrum in addition to the four known metastable (1s2s)¹ S ₀, (1s2s)³ S ₁, (1s2p)³ P ₂, and (1s2s2p)⁴ P _5/2 states in He- and Li-like systems. The states having lifetimes of about 10^?14s still contribute to the spectrum observed 10^?9s after the ions have passed a foil. This observation is explained by cascading processes from states of high principal quantum numbern≧14. The measured lifetime of the⁴ P _5/2 state subtracting the contribution of cascades is (0.594±0.016) ns and slightly larger than the theoretically predicted value of 0.563 ns. The³ P ₂ state is depopulated at short distances behind the foil by cascading processes. Its measured lifetime of (1.44±0.08) ns compares to a theoretical value of 1.48 ns.     

Metastable Decomposition of Ar3+ Cluster Ions Into Ar2+ and Ar+

In this note we present the first account of a study of metastable (unimolecular decay) and collision-induced dissociation of Ar₃+ cluster ions using an experimental setup consisting of a molecular beam-electron impact ion source and a double focussing (reversed Nier Johnson geometry) mass spectrometer. The existence of the following metastable decay processes (accessible by our sampling time window) could be demonstrated: Ar₃⁺* → Ar₂+ and Ar₃⁺* → Ar⁺. The processes were studied as a function of electron impact energy. The present results are of importance in order to provide some guidance for the development of appropriate theoretical models for the dissociation of cluster ions.     

Rotational and vibrational states of excitonic molecules in CuBr studied by the two-photon-resonant Raman scattering

Excited states of excitonic molecules are found in the study of the two-photon-resonant Raman scattering. These states consist of four levels and have binding energies of 1.0–1.8 meV, which are very small compared with those of the ground states. They are considered to be the rotational and vibrational states of excitonic molecules.