Ar?NO团簇的同步辐射光电离研究

利用国家同步辐射实验室合肥光源的真空紫外同步辐射，使NO分子和Ar原子混合物的超声分子束发生光电离，测量了Ar，NO和异类团簇Ar·NO的光电离效率谱. 在谱中，在与Ar原子的共振线对应的能量区域(11.5—12.0 eV)观察到一个强的类共振结构. 这个结果表明，在异类团簇Ar·NO的内部，稀有气体Ar原子的激发能转移到与它接触的分子NO上，使分子NO发生电离. 关键词： Ar·NO团簇 同步辐射 光电离 能量转移     

355 nm激光光电离甲醛飞行时间质谱的研究

利用脉宽为5 ns脉冲Nd: YAG 355 nm激光在功率密度为10¹¹–10¹² W/cm²条件下实现了甲醛含水团簇多光子电离, 并用飞行时间质谱对其电离产物和电离过程进行了研究. 实验中观测到了甲醛的质子化团簇系列 (CH₂O)_nH⁺(n=1–4), 甲醛的去质子化团簇系列(CH₂O)_nCHO⁺ (n=1–3), 以及两个起源于H₂CO去质子和质子化的含水团簇系列HCO⁺(H₂O)_n(n=1,3,5)和H₃CO⁺(H₂O)_n(n=1,3,5), 并对其中的一些团簇结构构型进行了猜测. 研究在不同的激光功率密度下甲醛团簇质谱峰的变换情况, 当激光密度达到9.3× 10¹¹ W/cm², 开始出现CH₂O和H₂O本体及其光致碎片的信号, 但对应的各质量峰没有明显地分辨开, 而是以包络的形式出现, 这是激光电离产生高能离子释放的一种表现, 提出认等离子体动力学鞘层加速机制(模型)来解释高能离子形成的物理机制. 关键词： 甲醛 团簇 飞行时间质谱 激光电离     

CS2团簇增强的激光多价电离现象的质谱研究

利用脉宽为25ns的脉冲Nd: YAG 532 nm的激光，在8×10¹⁰W/cm²的强度下，用飞行时间质谱对CS₂的激光电离过程进行了研究.观察到了较强的C²⁺和S²⁺高价离子信号，这些高价离子C²⁺，S²⁺的最可几平动能高达144 eV，112 eV.不同进样方式，激光延迟以及束源压力的实验结果表明，这些高价离子可能来源于CS₂团簇的库仑爆炸过程.多光子电离引发，逆韧致吸收加热-电子碰撞电离模型可能是高价离子产生的机理. 关键词： 2')" href="#">CS₂ 团簇 高价离子 激光电离     

原子团簇对飞秒激光的吸收

使用800nm飞秒脉冲激光研究了Xe,Ar,He等原子团簇对激光的吸收.实验结果表明,脉冲阀门的工作压力、所使用的气体种类等因素对团簇的尺寸及团簇对激光的吸收影响很大.在阀门工作压力为20×10⁵Pa、激光功率密度为1×10¹⁵W/cm²的条件下,Xe团簇对激光的吸收高达45%.激光预脉冲的存在会降低原子团簇对激光能量的吸收.离子能量测量结果表明,团簇对激光的高效吸收导致较高离子温度等离子体的生 关键词： 原子团簇 飞秒激光 能量吸收效率 高能离子     

Ar·CO团簇光电离的实验和理论研究

利用同步辐射光电离质谱装置,测量了Ar·CO范德瓦尔斯 (van der Waals, vdW) 团簇的的光电离质谱和光电离效率曲线.将它们与CO分子的绝对光吸收光谱比较, 发现在13.9到14.6 eV能量范围内的Ar·CO⁺的光电离效率曲线主要反映了收敛到 CO⁺ (X²∑⁺, v'= 1,2和3) Rydberg系列和收敛到 CO⁺ (A²Π)的n= 3的振动序列(v'= 6–9)的特点; 在14.6–15.75 eV光子能量范围内的Ar·CO的光电离效率曲线主要反映了CO的光吸收特性. 然而,由于Ar和CO之间的相互作用,其中的5个重要的光谱结构发生了蓝移; 而在15.75–15.80 eV光子能量范围内的Ar-CO的光电离效率曲线,它的属性受到组分Ar和CO的共同影响. 与此同时,也从理论上计算了Ar·CO团簇的电离能、Ar·CO团簇和Ar·CO⁺ 团簇离子的离解能. 关键词： Ar·CO团簇 同步辐射 光电离     

纳秒强激光中丙酮团簇增强的多价电离现象

利用脉宽为25 ns的脉冲Nd: YAG 532 nm的激光，在10¹⁰—10¹¹ W/cm²的强度下，用飞行时间质谱对丙酮团簇的激光电离过程进行了研究. 观察到了较强的O^q+(q=2—4)和C^q+(q=1—4)高价离子信号，这些高价离子 C⁴⁺，C³⁺，C²⁺，O⁴⁺，O³⁺，O²⁺的最大概然平动能分别为240 eV，70 eV，30 eV，90 eV，80 eV，40 eV. 高价离子的强度和平动能随激光强度的增大而增大. 我们提出一个多光子电离引发，逆韧致吸收加热-电子碰撞电离模型来解释高价离子的产生. 关键词： 丙酮 团簇 库仑爆炸 高价离子     

乙醚团簇在纳秒激光场中的多价电离及其电子能量分布的研究

用5ns,1064nm的脉冲Nd:YAG激光,研究了乙醚团簇与纳秒激光的相互作用.在10¹¹ W/cm²量级光强下,观察到价电子完全剥离的O⁶⁺,C⁴⁺,且这些高价离子的强度比值基本不随激光能量而变化.用阻滞电压方法测量了电离过程中溢出电子能量分布,在最大激光能量4.0×10¹¹ W/cm²,溢出电子的平均能量为56eV,最大能量为102eV.实验结果支持了高价离子产生的“多 关键词： 高价离子 电子能量 纳秒激光 乙醚团簇     

团簇增强的纳秒激光电离产生Xez+(z≤20)高价离子

利用功率密度为1011—1012W·cm-2的1064nm纳秒激光电离氙原子团簇，在飞行时间质谱中观察到电离态高达+20的高价离子.不同脉冲束位置实验表明，仅当激光作用于分子束的中段时，才能观察到高价离子，且高价离子的强度随束源压力的增加而迅速增强.实验结果表明束中大尺寸团簇的存在与高价离子的形成密切相关.讨论了高价离子产生的可能机理. 关键词： 氙 纳秒激光 高价离子 飞行时间质谱     

超短强激光脉冲激励甲烷团簇的内电离机理

采用三维粒子动力学模拟方法研究了甲烷团簇在超短强激光脉冲激励下的爆炸动力学行为,重点讨论了几种典型的内电离机理对团簇爆炸过程中离子的价态和动能的影响.研究表明,在激光脉冲强度比较小的情况下,团簇中的原子主要是在光场作用下通过隧道电离的方式发生电离.当激光场进一步增强时,势垒压低电离是电离的主要方式.在相同的较高激光强度下,团簇更容易通过势垒压低电离达到高的电离价态.团簇发生电离后,其内部库仑电场的点火电离效应和内部滞留自由电子的碰撞电离效应也将增强团簇的再次电离过程. 关键词： 超短强激光脉冲 甲烷团簇 内电离     

双驱动x射线激光等离子体能谱特性研究

用时间积分空间分辨的平晶千电子伏谱仪测量了钽激光等离子体发射波长范围为045— 075nm的软x射线能谱，精确测量和准确辨认出类镍、类钴和类铁离子的共振线及类镍离子 的内壳层跃迁线-对实验结果处理，获得了辐射线谱的强度-通过谱线比率的诊断推断脉冲激 光时差对等离子体状态的影响，至少也可部分解释激光上能级的粒子数及等离子体的 电离程度- 关键词： 离子谱特性 软x线能谱强度 谱线辨认     

Hindered Coulomb explosion of embedded Na clusters — stopping,shape dynamics and energy transport

We investigate the dynamical evolution of a Na₈ cluster embedded in Ar matrices of various sizes from N=30 to 1048. The system is excited by an intense short laser pulse leading to high ionization stages.We analyze the subsequent highly non-linear motion of cluster and Ar environment in terms of trajectories, shapes, and energy flow. The most prominent effects are: temporary stabilization of high charge states for several ps, sudden stopping of the Coulomb explosion of the embedded Na₈ clusters associated with an extremely fast energy transfer to the Ar matrix, fast distribution of energy throughout the Ar layers by a sound wave. Other ionic-atomic transfer and relaxation processes proceed at slower scale of few ps. The electron cloud is almost thermally decoupled from ions and thermalizes far beyond the ps scale.     

超强激光与Ar团簇相互作用中X射线的研究

本文主要研究了超强超短激光与Ar团簇相互作用过程中X射线能谱、K壳层光子产额、能量转换效率以及激光对比度对X射线光子产额的影响.实验中得到K壳层的光子产额约为1× 10¹¹/发,能量转换效率约为2.8× 10^-5．同时观测到较强预脉冲离化团簇会导致预电离,产生膨胀等离子体,然而主脉冲与膨胀的等离子体相互作用的强度较未膨胀时降低了,从而导致K壳层光子产额降低,而使用高对比度的激光能增加X射线光子产额.     

Ar原子团簇与飞秒强激光相互作用产生的高能离子计算

利用改进的“等离子体球”模型模拟了Ar原子团簇与飞秒强激光相互作用的物理过程.改进后的模型弱化了原模型在共振吸收附近团簇内部屏蔽电场的异常增强行为，从而使其更为合理，计算得到的Ar离子平均动能与以往的实验结果符合.还定量地研究了Ar离子平均动能及其平均电荷态与团簇尺寸以及激光参数之间的变化关系. 关键词： 团簇 飞秒激光 高能离子 共振吸收     

The structures and stabilities of mixed inert gas cluster ions: NeHe+ n and ArHe+ n

DIM-type matrices for RgHe⁺ _n clusters have been established from the results of ab initio calculations on RgHe and RgHe⁺ (Rg = Ne and Ar). The method has been tested against ab initio calculations on linear and T shaped RgHe⁺ ₂ and found to be satisfactory. Rotational invariance has been established for larger clusters, and the geometries and energies of clusters up to n = 16 have been determined. Ne cluster ions are more stable than Ar cluster ions because of the greater contribution from charge transfer, and are structurally different. The relative stabilities of these cluster ions are consistent with the available experimental data.     

Femtosecond ionization of magnesium clusters grown in ultracold helium droplets

Magnesium clusters grown in helium droplets and ionized with femtosecond laser pulses have been studied by high resolution mass spectrometry. For moderate laser intensities the abundance spectra show characteristic features indicating electronic shell effects. Compared to clusters of s¹-electron metals additional shell closures appear resulting from an electron rearrangement. Irradiation with higher laser intensities leads to a decomposition of the magnesium clusters into atomic ions. Due to charge exchange with the surrounding helium matrix mainly singly and doubly charged magnesium ions remain. In addition, the occurrence of MgHe_N ⁺-complexes is observed. Their abundance depends on the shape of the laser field, i.e. the laser width and the optical delay when applying the pump-probe technique. Received 2 January 2001     

Mössbauer effect of57Co in LiTaO3 — Effects of a variety of heat treatments

LiTaO₃ single crystals were doped with⁵⁷Co. Heat treatments of the crystals in the various atmospheres (Ar, Ar/H₂ etc.) very sensitively influenced the charge states of iron formed after the EC of⁵⁷Co. Fe²⁺ Fe³⁺ and metallic clusters are formed depending on the treatments in the various atmospheres. The observed effects were found reversible by changing the reducing and oxidising atmospheres.     

Resonant coupling of small size-controlled lead clusters with an intense laser field

We exposed small size-controlled lead clusters with a few hundreds of atoms to laser pulses with peak intensities up to 10¹⁵ W cm^-2 and durations between 60 fs to 2.5 ps. We measured kinetic energies and ionic charge of fragments as a function of the laser intensity and pulse duration. Highly charged Pbⁿ⁺ ions up to n = 26 have been detected presenting kinetic energies up to 15 keV. For comparison with our experimental results, we have performed simulations of the laser coupling with a cluster-sized lead nanoplasma using a qualitative model that was initially proposed by Ditmire and co-workers at LLNL for the case of rare gas clusters. From these simulations we conclude that two mechanisms are responsible for the explosion dynamics of small lead clusters. As already observed for large rare gas clusters (n = 10⁶), fragments with charge states below +10 are driven by Coulomb forces, whereas the higher charged fragments are accelerated by hydrodynamic forces. The latter mechanism is a direct consequence of the strong laser heating of the electron cloud in the nanoplasma arising from a plasmon-like resonance occurring at n _e = 3n _c. In order to obtain an optimized laser-nanoplasma coupling, our results suggest that the plasma resonance should occur at the peak intensity of the laser pulse. Due to inertial effects, even for such small-sized clusters, the observed optimum pulse duration is in the order of 1 ps which is in good agreement with our theoretical results. Received 18 March 2002 Published online 19 July 2002     

Study on the interaction of intense femtosecond laser pulses with nanometre-sized hydrogen clusters

The interaction of intense femtosecond laser pulses with hydrogen clusters has been experimentally studied. The hydrogen clusters were produced from expansion of high-pressure hydrogen gas (backed up to 8\tm10⁶Pa) into vacuum through a conical nozzle cryogenically cooled by liquid nitrogen. The average size of hydrogen clusters was estimated by Rayleigh scattering measurement and the maximum proton energy of up to 4.2keV has been obtained from the Coulomb explosion of hydrogen clusters under 2×10¹⁶ W/cm² laser irradiation. Dependence of the maximum proton energy on cluster size and laser intensity was investigated, indicating the correlation between the laser intensity and the cluster size. The maximum proton energy is found to be directly proportional to the laser intensity, which is consistent with the theoretical prediction.     

Highly charged ions from laser-cluster interactions: local-field-enhanced impact ionization and frustrated electron-ion recombination

Our molecular dynamics analysis of Xe_{147-5083} clusters identifies two mechanisms that contribute to the yet unexplained observation of extremely highly charged ions in intense laser cluster experiments. First, electron impact ionization is enhanced by the local cluster electric field, increasing the highest charge states by up to 40%; a corresponding theoretical method is developed. Second, electron-ion recombination after the laser pulse is frustrated by acceleration electric fields typically used in ion detectors. This increases the highest charge states by up to 90%, as compared to the usual assumption of total recombination of all cluster-bound electrons. Both effects together augment the highest charge states by up to 120%, in reasonable agreement with experiments.     

飞秒激光惰性气体Ar原子多次电离过程的空间分辨研究

使用100飞秒、1014 W/cm2的强激光与惰性气体Ar原子相互作用,我们利用飞行时间质谱仪结合Z扫描技术获得了各次电离的Ar原子在激光焦点附近不同位置处强度分布.测量得到的各个不同电离态Ar n+(n=1～4)的产额随激光焦点位置变化关系与不同电离态的空间分布理论预言相一致.