2.1GeV?Kr离子在聚碳酸酯膜中引起的辐照效应研究

用傅立叶变换红外光(FTIR)谱仪和紫外/可见光(UV/VIS)谱仪研究了2.1GeVKr离子在聚碳酸酯(PC)膜中产生的效应.研究结果表明,在高能Kr离子辐照下,PC膜中发生了断键、断链和键的重组,炔基的出现是键的断裂和重组的结果.这些效应与辐照剂量和电子能损有关.辐照也使PC膜中发生了从氢化非晶态碳向非晶态碳的转变,在UV/VIS中,波长为380,450和500nm处的相对吸光度随能量沉积密度的增加近似按线性变化.     

红外光吸收研究35MeV/u Ar离子辐照半晶质聚酯膜引起的效应

35MeV/u Ar离子在室温下辐照了多层堆叠的半晶质聚酯膜,采用傅立叶转换的红外光吸收技术分析和研究了由辐照引起的化学键断裂及其对离子剂量、离子在样品中的平均电子能量损失和吸收剂量的依赖性.结果表明,辐照导致聚酯膜中发生了明显的化学键断裂,断键过程主要发生在反式构型的乙二醇残留物和苯环的对位上,苯环的基本结构在辐照中变化较小.断键不仅强烈地依赖于离子的照射剂量,而且还跟样品中电子能量沉积密切相关,明显的断键发生在4.0MGy以上的吸收剂量.     

质子辐照铝膜反射镜的慢正电子湮没研究

采用分光光度计测定了60keV质子辐照后铝膜反射镜反射光谱的变化规律.用慢正电子湮没等分析技术研究了辐照损伤的微观机制.结果表明，当质子辐照主要作用于反射镜铝膜层中时反射镜在200—800nm波长范围内反射率随辐照剂量增加而下降.入射质子可对铝膜中的缺陷产生填充作用，减小铝膜中电子密度，增加弱束缚电子带间跃迁.紫外至可见光能量较高的波段可引起带间激发跃迁，使相应的谱段反射率下降，导致反射镜光学性能的退化. 关键词： 反射镜 光学性能 质子辐照 慢正电子湮没     

n-GaN肖特基势垒光敏器件的电子辐照效应

本文主要研究了n型GaN肖特基紫外光敏器件(包括GaN肖特基势垒紫外探测器,GaN肖特基二极管)的电子辐照效应和失效机理,以及辐照后二极管对不同波长光的光敏特性的变化。从实验中观测到,随着辐照注量的不断增加,GaN光敏器件的击穿电压明显减小,反向漏电流逐渐增大。证实了辐照后Au/GaN间产生的界面态是引起GaN肖特基势垒光敏器件辐照失效的原因。另外,在研究辐照效应对GaN肖特基二管光敏特性的影响时观测到,经过一定剂量的辐照后,GaN肖特基二管能探测到380nm的紫外光和可见光,而在辐照以前,它是探测不到的。这说明辐照效应将导致肖特基势垒光敏器件对较长波长的吸收,使得UV探测器中可见光成分的背景噪声增加。     

22 MeV/u的Fe离子在PET 膜中引起的辐照效应研究

用能量为22 MeV/u的 Fe离子在室温和真空条件下辐照了多层堆叠的半晶质聚酯膜, 采用傅里叶转换红外吸收光谱、 紫外/可见吸收光谱 和X射线衍射技术分析测量了辐照后聚酯膜的微观结构所发生的变化, 详细研究了分子结构的变化和非晶化转变与离子剂量、 离子在样品中的平均电子能损以及吸收剂量的依赖关系． 分析结果表明: 辐照导致化学键的断裂、 新化学键的形成和非晶化转变． 非晶化效应和化学键的断裂随离子剂量和电子能损的增加而增大, 但变化的总量仅依赖于总的吸收剂量, 表明在所涉及的能损范围里, 辐照产生的变化与辐照离子的种类和能量没有直接的关系, 而只决定于材料对辐照离子能量的吸收程度． Semicrystalline polyethylene terephthalate (PET) film stacks were irradiated with 22 MeV/u Fe ions at room temperature under vacuum. Ion beam induced microscopic structural modifications and amorphous transformation were investigated by means of Fourier transform infrared spectrosocopy (FTIR), ultraviolet visible absorption spectrosocopy (UV/Vis) and X ray diffractometer (XRD). It was found that irradiation induces bond breaking, formation of new free radiculs and amorphous transformation. These effects were found to depend on ion fluence , the electronic energy loss and aborbed dose. The creation of alkyne groups was found only at the aborbed dose higher than 5.0 MGy.     

第一性原理研究O和S掺杂的石墨相氮化碳(g-C_3N_4)_6量子点电子结构和光吸收性质

利用密度泛函和含时密度泛函理论研究了氧(O)和硫(S)原子掺杂的石墨相氮化碳(g-C_3N_4)_6量子点的几何、电子结构和紫外-可见光吸收性质.结果表明:掺杂后(g-C_3N_4)_6量子点杂质原子周围的C-N键长发生了一定的改变,最高电子占据分子轨道-最低电子未占据分子轨道(HOMO-LUMO)能隙显著减小.形成能的计算表明O原子取代掺杂的(g-C_3N_4)_6量子点体系更稳定,且O原子更易取代N3位点,而S原子更易取代N8位点.模拟的紫外-可见电子吸收光谱表明,O和S原子的掺杂改善了(g-C_3N_4)_6量子点的光吸收,使其吸收范围覆盖了整个可见光区域,甚至扩展到了红外区.而且适当的杂质浓度使(g-C_3N_4)_6量子点光吸收在强度和范围上都得到明显改善.通过O和S掺杂的比较,发现二者在可见光区对(g-C_3N_4)_6量子点的光吸收有相似的影响,然而在长波长区域二者的影响有明显差异.总体而言,O掺杂要优于S掺杂对(g-C_3N_4)_6量子点光吸收的影响.     

~(12)C~(6 )离子辐照小鼠Lewis肿瘤的研究

研究了HIRFL提供的12C6 离子辐照C57BL/6J小鼠右后腿移植的Lewis肿瘤的生长延迟和碳离子辐照对Lewis肿瘤小鼠寿命的延长.结果表明,碳离子照射的小鼠肿瘤生长体积明显地小于对照的体积.在剂量相同、分次数辐照越多时,肿瘤生长就越缓慢,肿瘤抑制就越高.在辐照分次数相同时,不同剂量对受照肿瘤生长体积未产生差异.在4Gy×3,8Gy×3和12Gy×2组3种辐照剂量下,小鼠寿命的P值小于0.05;可知小鼠的寿命延长具有统计学意义.     

不同离子辐照氟化锂材料时原位发光光谱测量分析

在BNU400注入机上搭建的离子激发发光(ion beam induced luminescence,IBIL)测量装置上,开展了相同能量(100 keV)条件下的3种离子(H~+、He~+以及O~+)辐照氟化锂材料时的IBIL光谱的原位测量工作,对比研究离子种类对氟化锂材料辐照缺陷的生成及其演变行为的影响.结合SRIM(Stopping and Range of Ions in Matter)模拟的结果,可以发现He~+辐照时的IBIL光谱强度最高,这是由于He~+激发产生的电子空穴对密度高于H~+,而O~+辐照时由于激发出的电子空穴对密度过高引起的非辐射复合比例增加,从而导致发光效率过低;质量数越大的离子辐照时,核阻止本领越大,会加快缺陷的生成和湮灭速率,降低达到平衡状态时的发光强度.近红外波段的F_3~-/F_2~+色心发光峰强度及其演变行为表明其耐辐照性能好于可见光波段的F_2色心.     

645 MeV Xe35+离子辐照SiO2在线光发射的研究

离子辐照可以改变二氧化硅(SiO₂)的晶体结构和光学性质.采用645 MeV Xe³⁵⁺离子辐照SiO₂单晶,在辐照过程中,利用光栅光谱仪测量在200—800 nm范围内的光发射.在发射光谱中,观测到中心位于461和631 nm的发射带.这些发射带是弗伦克尔激子辐射退激产生的,其强度与辐照离子能量和辐照离子剂量密切相关.实验结果表明:发射光强随离子在固体中的电子能损呈指数增加.由于离子辐照对晶体造成损伤,发射光谱强度随辐照剂量的增加而降低.文中讨论了这些与晶体结构有关的发射带,结合能量损失机制讨论了激子形成和退激过程.快重离子辐照过程中发射光谱的原位测量对研究辐照改性具有重要意义,有助于揭示离子辐照引起晶体损伤的物理机制.     

高能氩离子在聚苯乙烯中的电子能损效应研究

用1.4GeV氢离子对多层堆叠的厚约53m的聚苯乙烯薄膜在室温和真空条件下进行了辐照;对辐照后的样品进行了从红外到紫外的光吸收测量.测量结果显示,材料经高能红离子辐照后发生化学降解,降解过程强烈依赖于电子能损;在能量沉积密度很高的径迹芯中,分子主链和苯环均遭到破坏;在电子能损高于0.77keV/nm时有炔基产生.     

Swift Heavy Ion Irradiated Low-Density Polyethylene: Structural and Optical Investigations

Abstract

The structural and optical effects of copper (50?MeV) and carbon (70?MeV) ion irradiation of low density polyethylene (LDPE) are described. X-ray diffraction (XRD) and differential scanning calorimetric (DSC) techniques were used to explore the structural behavior, while Fourier transform infrared (FTIR) and UV-visible spectroscopies were used to collect the optical data. Structural parameters, such as interplanar separation, distortion factor, crystallite size and degree of crystallinity, were measured to understand the change in the structural behavior of LDPE caused by the swift heavy ion irradiation. In the irradiated polymeric samples, the formation and growth of new carbon enriched species were revealed by the FTIR and UV-visible analysis, which led to the decrease of their optical bandgap energy with the increase of ion fluence.     

Optical and Structural Modifications in Heavy Ion Irradiated Polystyrene

Samples of polystyrene (PS) have been irradiated with ⁶⁴Cu (50 and 120 MeV) and ¹²C (70 MeV) ion beams (fluence=10¹¹ to 10¹³ ions cm^?2) in order to study the induced modifications using UV‐VIS and FTIR spectroscopy. UV spectra of irradiated samples reveal that the optical band gap decreases from 4.36 to 1.46 eV in PS. The decrease in optical band gap is more pronounced with the Cu‐ion beam due to high electronic energy loss as compared to the C ion beam. The effect of low energy (50 MeV) Cu ions on the optical properties of PS is larger than that due to high energy (120 MeV) Cu ions. The correlation between the optical band gap and the number of six member carbon rings inside the largest carbon clusters embedded in the network of polystyrene is discussed. FTIR spectra reveal the formation of hydroxyl, alkene, and alkyne groups in the Cu‐ion irradiated PS. Changes in the intensity of the absorption bands on irradiation with C‐ion relative to pristine samples have also been observed and are discussed.     

Carbon (70 MeV) and copper (120 MeV) ions irradiation effects in Makrofol-N

Makrofol-N polycarbonate was irradiated with carbon (70 MeV) and copper (120 MeV) ions to analyze the induced effects with respect to optical and structural properties. In the present investigation, the fluence for carbon and copper beams was kept in the range of 1×10¹¹– 1×10¹³ ions/cm² to study the swift heavy ion induced modifications. UV–VIS, FTIR and XRD techniques were utilized to study the induced changes. The analysis of UV–VIS absorption studies revealed that the optical energy gap was reduced by 17% on carbon irradiation, whereas the copper beam leads to a decrease of 52% at the highest fluence of 1×10¹³ ions/cm². The band gap can be correlated to the number of carbon atoms, N, in a cluster with a modified Robertson's equation. In copper (120 MeV) ions irradiated polycarbonate, the number of carbon atoms in a cluster was increased from 63 to 269 with the increase of ion fluence from 0 to 1×10¹³ ions/cm², whereas N is raised only up to 91 when the same polymer films were irradiated with carbon (70 MeV) ions under similar conditions. FTIR analysis showed a decrease in almost all characteristic absorption bands under irradiation. The formation of hydroxyl (? OH) and alkene (C?C) groups were observed in Makrofol-N at higher fluence on irradiation with both types of ions, while the formation alkyne end (R? C≡ CH) group was observed only after copper ions irradiation. The radii of the alkyne production of about 3.3 nm were deduced for copper (120 MeV) ions. XRD measurements show a decrease in intensity of the main peak and an increase of the average intermolecular spacing with the increase of ion fluence, which may be attributed to the structural degradation of Makrofol-N on swift ion irradiation.     

Copper (50 MeV) and Oxygen (84 MeV) Ion Irradiation Probed Thermal,Structural and Optical Behavior of Polyethylene Terephthalate

Polyethylene terephthalate (PET) films of 50?μm thickness were exposed to swift-heavy 50?MeV copper and 84?MeV oxygen ions, with fluence varying from 1?×?10¹¹ to 1?×?10¹³ ions cm^?2. Differential scanning calorimetry (DSC), X-ray diffraction (XRD) and Fourier-transform infrared (FTIR) and UV-visible spectroscopic techniques were used to characterize the irradiated samples. The XRD and DSC analysis indicated the loss of crystallinity during/after the irradiation. The FTIR spectra revealed the formation of alkyne end groups, C═C groups and structural deformation with increase of ion fluence. Considerable reduction in the value of the optical bandgap was inferred from the study of the UV-visible absorption curves.     

Surface modification of Makrofol-DE induced by α-particles

In the present work, Makrofol DE samples were irradiated with different doses of alpha particles. The optical and mechanical modifications in the alpha-irradiated Makrofol samples as a function of alpha irradiation time have been investigated. Different characterization techniques, UV–vis spectroscopy, photoluminescence spectroscopy and Vickers micro hardness tester have been used. UV–vis spectra of bombarded samples reveal that the optical absorption increases with increasing the irradiation time. The direct and indirect optical band gap was found to decrease from 3.4 and 2.81?eV for pristine sample to 3.1 and 2.35?eV for that bombarded with alpha particles at the highest irradiation time (15?h), respectively. The number of carbon atoms per conjugated length (N) and the number of carbon atoms per cluster (M) have been estimated. An increase in both N and M with increasing the irradiation time was noticed. A remarkable decrease in PL intensity with increasing the alpha irradiation time was observed. This decrease is attributed to ion beam-induced change in molecular structure and/or defects in the modified layer. The surface hardness for unmodified and modified polymeric material has been studied.     

Swift heavy ion irradiation effects on structural,optical properties and ac conductivity of polypyrrole nanofibers

Polypyrrole (PPy) nanofibers have been synthesized by interfacial polymerization method and irradiated with 160?MeV Ni¹²⁺ ions under vacuum with fluences in the range of 10¹⁰–10¹²?ions/cm². High-resolution transmission electron microscopy results show that upon swift heavy ion (SHI) irradiation the PPy nanofibers become denser. The crystallinity of PPy nanofibers increases upon SHI irradiation, while their d-spacing decreases. Upon SHI irradiation, the polaron absorption band gets red-shifted indicating reduction in the optical band gap energy of the irradiated PPy nanofibers. The indirect optical band gap energy is decreased as compared to corresponding direct optical band gap energy. The number of carbon atoms per conjugation length (N) and carbon atoms per cluster (M) of the SHI-irradiated PPy nanofibers increase with increasing the irradiation fluence. Fourier transform infrared spectra reveal the enhancement in intensity of some characteristic vibration bands upon SHI irradiation. The thermal stability of the PPy nanofibers is enhanced on SHI irradiation. The charge carriers in both pristine and irradiated PPy nanofibers follow the correlated barrier hopping mechanism. Scaling of ac conductivity reveals that the conduction mechanism is independent of the SHI irradiation fluence.     

Electron-beam irradiation effects on poly(ethylene-co-vinyl acetate) polymer

Poly(ethylene-co-vinyl acetate) (EVA) films were irradiated with a 1.2 MeV electron beam at varied doses over the range 0–270 kGy in order to investigate the modifications induced in its optical, electrical and thermal properties. It was observed that optical band gap and activation energy of EVA films decreased upon electron irradiation, whereas the transition dipole moment, oscillator strength and number of carbon atoms per cluster were found to increase upon irradiation. Further, the dielectric constant, the dielectric loss, and the ac conductivity of EVA films were found to increase with an increase in the dose of electron radiation. The result further showed that the thermal stability of EVA film samples increased upon electron irradiation.     

Effect of 100 MeV O7+ ion beam irradiation on structural,optical and electronic properties of SnO2 thin films

In this paper, we present the impact of swift heavy ion beam irradiation on the structural, optical and electronic properties of SnO₂ thin films. Thin films were deposited using the pulsed laser deposition technique on Al₂O₃ substrates. Atomic force microscopy, X-ray diffraction, UV–visible absorption and temperature-dependent resistivity measurements were performed to explore the morphological, structural, optical and electronic properties of the as-deposited and irradiated samples. The peak intensity of the (200) peak was found to decrease monotonously with increasing irradiation fluence. The band gap energy of the 1×10¹¹ ion/cm² irradiated sample was found to increase. The electrical resistivity of the samples showed a continuous increase with the irradiation fluence.     

多元纳米稀土六硼化物Nd1-xEuxB6粉末的制备及光吸收研究

在真空环境中采用固相烧结法成功制备出了多元稀土六硼化物Nd1-xEuxB6纳米粉末.系统研究了Eu掺杂对纳米NdB6物相、形貌及光吸收性能的影响规律.结果表明,所有合成的纳米粉末物相均为单相的CsCl型晶体结构,具有立方形貌,平均晶粒尺度为30 nm.光吸收实验结果表明,随着Eu掺杂量的增加,纳米NdB6透射光波长从629 nm红移至1000 nm以上,表现出了透射光波长的可调特性.此外,NdB6和EuB6同步辐射吸收图谱表明,Nd和Eu原子分别以Nd^3+和Eu^2+形式存在于纳米NdB6和EuB6中,充分说明了Eu掺杂使NdB6传导电子数量减少,从而导致其等离子共振频率能量的降低.采用第一性原理计算了NdB6和EuB6的能带结构、态密度、介电函数以及等离子共振频率能量,从而定性解释了Eu掺杂使NdB6透射光波长红移的特性.     

Effect of Ar bombardment on the electrical and optical properties of low-density polyethylene films

The influence of low-energy Ar ion beam irradiation on both electrical and optical properties of low-density polyethylene (LDPE) films is presented. The polymer films were bombarded with 320 keV Ar ions with fuences up to 1×10¹⁵ cm^?2. Electrical properties of LDPE films were measured and the effect of ion bombardment on the DC conductivity, dielectric constant and loss was studied. Optically, the energy gap, the Urbach’s energy and the number of carbon atoms in a cluster were estimated for all polymer samples using the UV–Vis spectrophotometry technique. The obtained results showed slight enhancement in the conductivity and dielectric parameters due to the increase in ion fluence. Meanwhile, the energy gap and the Urbach’s energy values showed significant decrease by increasing the Ar ion fluence. It was found that the ion bombardment induced chain scission in the polymer chain causing some carbonization. An increase in the number of carbon atoms per cluster was also observed.