Preparation of graphene on SiC by laser-accelerated pulsed ion beams

Laser-accelerated ion beams (LIBs) have been increasingly applied in the field of material irradiation in recent years due to the unique properties of ultra-short beam duration, extremely high beam current, etc. Here we explore an application of using laser-accelerated ion beams to prepare graphene. The pulsed LIBs produced a great instantaneous beam current and thermal effect on the SiC samples with a shooting frequency of 1 Hz. In the experiment, we controlled the deposition dose by adjusting the number of shootings and the irradiating current by adjusting the distance between the sample and the ion source. During annealing at 1100 ℃, we found that the 190 shots ion beams allowed more carbon atoms to self-assemble into graphene than the 10 shots case. By comparing with the controlled experiment based on ion beams from a traditional ion accelerator, we found that the laser-accelerated ion beams could cause greater damage in a very short time. Significant thermal effect was induced when the irradiation distance was reduced to less than 1 cm, which could make partial SiC self-annealing to prepare graphene dots directly. The special effects of LIBs indicate their vital role to change the structure of the irradiation sample.     

Pulsed laser deposition of pure fluoroapatite film without OH groups

The relation between O₂ pressure and composition in the pulsed‐laser deposition of fluoroapatite was investigated using both on‐axis and off‐axis methods to determine the optimal conditions for obtaining a pure fluoroapatite film without OH groups. Through this, it was found that an O₂ pressure of 10 Pa, combined with an off‐axis method, results in P/Ca and F/Ca values (0.6 and 0.2, respectively) that match closely with a stoichiometric composition of Ca₁₀(PO₄)₆F₂. Fourier transform infrared spectroscopy analysis confirmed that this optimized film was almost pure fluoroapatite, with no evidence of any OH groups originating from hydroxyapatite. X‐ray diffraction also revealed that this fluoroapatite film crystallizes with a c‐axis orientation perpendicular to its surface.     

Surface analysis of ripple pattern on PS and PEN induced with ring‐shaped mask due to KrF laser treatment

The approach for ripple nanopattern construction on surface of two polymer substrates [polyethylene naphthalate (PEN) and polystyrene (PS)] exposed by a KrF pulse excimer UV laser through a contact lithographic mask with circular slit was proposed in this paper. Thin layer of gold was deposited on samples after the laser treatment. Changes in the morphology of the surface of both the shielded and exposed areas of the substrates, as well as the dimensions of the laser‐induced periodic surface structures, were determined (by atomic force microscopy, laser confocal microscopy and scanning electron microscopy), compared with observations and measurements made on samples treated directly (without a contact mask) under the same conditions. The morphology of the interface between the treated and untreated regions was also closely studied. Surface chemistry of treated samples was studied in detail by X‐ray Photoelectron Spectroscopy. The detailed study of surface chemistry of modified PEN and PS revealed a significant increase of oxygen concentration for laser treated PS and increase of carboxyl groups in case of PEN. The potential application of this research can be found in biotechnology, micro technology and several other fields. Copyright © 2016 John Wiley & Sons, Ltd.     

Coarse Metal Powder-Assisted pulsed CO2 Laser-induced Breakdown Spectroscopy for the Direct Determination of Heavy Metals in Soil

A novel method of laser-induced plasma spectroscopy utilizing a pulsed transversely excited atmospheric CO₂ laser has been developed for the high-sensitivity determination of heavy metals in soil. A coarse metal powder was used to trap the soil and to assist with plasma generation. When the CO₂ laser (10.6?µm, 1.5?J, 200?ns) was irradiated on the metal and soil powder, a high-temperature and long-lifetime luminous plasma was induced. Fine particles of soil were dissociated and were excited in the plasma region. The method was used for the rapid determination of Cr, Pb, and Hg in loam. The limits of detection for Cr, Pb, and Hg were approximately 0.8, 15, and 0.7?mg/kg, respectively.     

Calibration for Elemental Dental Tissue Analysis by Laser Ablation Inductively Coupled Plasma Mass Spectrometry

Teeth retain different elements at particular stages of life. Hence, the exposure over a selected time span may be characterized by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). A Nd:YAG laser with emission at 266?nm was coupled to a quadrupole ICP-MS for the quantitative study of historical human teeth for Sr and Ba, elements of anthropological significance. A calibration approach incorporating the experimentally derived k coefficient is reported. The coefficients were established based on the mean concentrations of the analytes determined by pneumatic nebulization ICP-MS using acid-digested calcium phosphate standards and the intensities recorded during laser ablation of corresponding standards as pellets. The k values were 0.54?±?0.05 (µg?g^?1)^?1 and 4.49?±?1.09 (µg?g^?1)^?1 for Sr and Ba, respectively. This calibration approach provided local quantitative data and demonstrated statistically significant differences in Sr concentrations in enamel and dentine.     

Phosphoprotein Analysis by MALDI-TOF Mass Spectrometry using On-Probe Tandem Proteolysis and Dephosphorylation

In this investigation, methods based on on-probe enzymatic cleavage matrix-assisted laser desorption/ionization time-of-flight mass spectrometric (MALDI-TOF-MS) analyses have been developed, allowing the rapid assignment of phosphorylation sites within phosphoproteins. The procedures involved robotic sample deposition of a phosphoprotein, such as intact bovine β-casein, on stainless steel or gold MALDI plates, on-probe proteolysis with trypsin for 10–180?s at 37°C, on-probe dephosphorylation for 1–10?min at 37°C with alkaline phosphatase, followed by differential mass spectrometry with peptide mass mapping. The dephosphorylation conditions were initially optimized using in-solution tryptic digestion of the phosphoprotein performed in the presence of MS-compatible anionic surfactant sodium 3-[(2-methyl-2-undecyl-1,3-dioxolan-4-yl)methoxy]-1-propanesulfonate. Two methods of trypsin deactivation were investigated, cooling and quenching by acidification, which resulted in the surfactant either staying intact or becoming cleaved, respectively. Since the surfactant had no detrimental effects on dephosphorylation of phosphopeptides, the acidification and neutralization steps were not included in the final analytical method. A protocol, comprising on-probe tandem, surfactant-aided proteolysis for 3?min followed by on-probe dephosphorylation for 10?min was thus established, allowing the rapid identification of location and sequence of phosphopeptides within a phosphoprotein by these procedures.     

Progress in thermal-mechantical effects induced by laser

对激光辐照诱导的热与力学问题研究进展进行了综述,包括材料在高温、高升温速率下的本构关系,典型薄板和柱壳等结构在激光辐照下的热力破坏效应,多层材料体系的激光破坏行为等几个方面,并着重介绍了包含相变与烧蚀过程的激光破坏分析模型与机制研究,激光辐照效应的流-热-固耦合数值模拟方法,以及短脉冲激光引起的冲击与破坏机理等方面的研究新进展.     

激光辐照下有界圆厚板的热弹性弯曲响应分析

考虑板弯曲运动的旋转惯性效应和剪切变形效应，建立了轴对称热能沉积作用下，边界固支或简支圆厚板的热弹性弯曲运动控制方程。利用数学变换和摄动法，导出了各种温度－力学边界条件下板的热弹性弯曲挠度及截面广义转角的解析公式。给出了在空间Ｇａｕｓｓ型分布激光束辐照下，板整体弯曲响应的代表性数值计算结果，直观显示了板弯曲挠度的时空变化规律。     

关于激光捷联惯性导航系统姿态算法的分析

圆锥误差和量化误差是激光捷联惯性导航系统姿态解算误差的两个最主要的误差源.从分析圆锥误差产生的机理出发,分别分析了以角度和角速度为计算参数的圆锥误差补偿算法,并对量化误差对圆锥误差补偿算法的影响进行了研究.通过理论分析和数字仿真,得出在实际工程应用中,采用角速度为输入信息的激光捷联惯性导航系统姿态算法应该在考虑量化误差的情况下,采用以角速度为计算参数的圆锥误差补偿算法.     

Boundary layer effect on thermal NO decomposition behind incident shock waves

The thermal decomposition of nitric oxide (diluted in Argon) has been measured behind incident shock waves by means of IR diode laser absorption spectroscopy. In two independent runs the diode laser was tuned to the=0 =1² _3/2 R(18.5)-rotational vibrational transition and the=1 =2² _3/2 R(20.5)-rotational vibrational transition of nitric oxide, respectively. These two transitions originating from the vibrational ground state (=0) and the first excited vibrational state (=1) were selected in order to probe the homogeneity along the absorption path. The measured NO decomposition could satisfactorily be described by a chemical reaction mechanism after taking into account boundary layer corrections according to the theory of Mirels. The study forms a further proof of Mirels' theory including his prediction of the laminar-turbulent transition. It also shows, that the inhomogeneities from the boundary layer do not affect the IR linear absorption markedly.This article was processed using Springer-Verlag T_EX Shock Waves macro package 1.0 and the AMS fonts, developed by the American Mathematical Society.