Real-time evolution of ion–surface interactions of MgAl2O3 and LiNbO3 detected by ion-induced photon spectroscopy

Ion-induced photon emission under 60 keV Cu⁻ implantation into the insulators of MgAl₂O₄ and LiNbO₃ was in situ measured over a wide wavelength range from 200 to 900 nm. The formation of the Mg and Li deficient layers for the respective insulator was detected based on the dose dependence of the Al, Mg and Li atomic line intensities. The Al I and Mg I line intensities from spinel exhibit different behaviors depending on irradiation temperatures: they gradually decrease while the (Al I)/(Mg I) ratio increases up to dose of 3×10¹⁷ ions/cm² at room temperature or exhibits a steady-state tendency at high temperature. Sharp decrease of Li I line intensity from LiNbO₃ under high dose rate bombardment indicates drastic changes of surface layer that may alter the phase stability and optical performance of insulators.     

Structural changes in anatase TiO2 thin films irradiated with high-energy heavy ions

In order to investigate possible structural changes due to high-density electronic excitation, anatase TiO₂ thin film specimens were irradiated with 230 MeV ¹³⁶Xe¹⁵⁺ ions and 200 MeV ¹⁹⁷Au¹³⁺ ions. X-ray diffraction (XRD) patterns were measured before and after irradiation. The intensity of the XRD peak assigned to the (0 0 4) planes of anatase TiO₂ decreases in an exponential manner as a function of ion-fluence. This result can be explained by the formation of the cylindrical damaged regions (i.e. ion tracks) with diameters of 9.6 and 16.3 nm for 230 MeV Xe and for 200 MeV Au ion irradiations, respectively. The difference in the track diameter between Xe ion irradiation and Au ion irradiation can be attributed to the difference in the electronic stopping power (and to the ion-velocity effect, if any). For 200 MeV Au ion irradiation, splitting of the (0 0 4) peak is observed. The original (0 0 4) TiO₂ peak remains in the same position, but the new peak shifts to higher angles as fluence increases.     

Atomic structure and disordering induced by 350 MeV Au ions in MgAl2O4

Microstructure change and atomic disordering in MgO · nAl₂O₃ (n = 1.1) irradiated with 350 MeV Au ions (S_e = 35 keV/nm) were investigated through transmission electron microscopy (TEM) and high angular resolution electron channeling X-ray spectroscopy (HARECXS) techniques. High resolution TEM revealed that each ion track maintains crystalline structure. The core region of ion track is found to reveal a lattice fringe with a half period of spinel matrix, suggesting the phase transformation from spinel to rock-salt structure. HARECXS analysis clearly showed progress of cation disorder at a significantly large region of 10 nm in diameter. These results are compared with the previous results of 200 MeV Xe ion irradiated spinel (S_e = 25 keV/nm). The structure of ion tracks is found to consist of three concentric circle structures: the defective core region (2 nm in diameter), strained region (5 nm) and cation disordered region (10–12 nm).     

Surface nanostructuring of SrTiO3 single crystals by slow highly charged ions and swift heavy ions

Single crystals of strontium titanate have been irradiated with both slow highly charged Xe ions extracted from an Electron Beam Ion Trap and swift heavy Xe ions. After irradiation, the crystals were investigated by scanning force microscopy in air. In both cases nanohillocks due to impact of individual projectiles were observed. This similarity originates from the fact that both swift heavy ions and slow highly charged ions initially transfer their energy to the electronic system of the target, leading to a localized region of high electronic excitation. This electronic excitation is subsequently transferred to the lattice atoms by electron-phonon coupling, leading to pronounced lattice heating. The formation of surface hillocks can then be ascribed to a melting process. We also present first evidence for the existence of a potential energy threshold for nanohillock formation on strontium titanate surfaces by slow highly charged ions.     

Interaction of energetic clusters (Au3, Au400 and C60) with organic material and adsorbed gold nanoparticles

Using molecular dynamics simulations (MD), this contribution compares the interaction of three energetic clusters (Au₃, Au₄₀₀ and C₆₀) with a hybrid surface of crystalline polyethylene (PE) covered by a layer of gold nanoparticles. This model system mimics the situation encountered in metal-assisted secondary ion mass spectrometry. The chosen impact points are representative of the PE surface, the metal particles and the frontier between the metal and the polymer. The simulations show the differences between the impact over the Au nanoparticle and the polymer surface, in terms of projectile penetration, crater formation and sputtering yield of PE and gold species. For C₆₀ and Au₃ projectiles, a simple correlation is found between the quantity of energy deposited in the top polymeric layers and the quantity of sputtered polymer material, including all the impact points. The results obtained with Au₄₀₀ do not fit on this line, indicating that other physical parameters are prevalent. The mechanistic view of the interaction provided by the MD helps explain the differences. In short, while C₆₀ and Au₃ quickly break apart, creating energetic recoils and severing many bonds in the surface, Au₄₀₀, with the largest total momentum by far (∼10 times larger than the others) and the lowest energy per atom (25 eV), tends to act and implant in the solid as a single entity, pushing the polymeric material downwards and breaking few bonds in the surface.     

Surface modification of MgAl2O4 and oxides with heavy ions of fission fragments energy

In this paper we report on results of surface modification in several candidate materials for inert matrix fuel hosts (MgAl₂O₄, MgO and Al₂O₃) induced by (0.5–5) MeV/amu Kr, Xe and Bi ion bombardment in the fluence range of 2 × 10¹⁰–10¹² ions/cm². The size and shape of nanoscale hillock-like defects, each of which was created by the impact of a single ion, have been studied by using atomic force microscopy (AFM) technique. It was found that mean hillock height on sapphire and spinel surfaces depends linearly on the incident electronic stopping power. The hillocks are highest in MgAl₂O₄, having a lower threshold for the lattice disorder in the bulk material via relaxation of electronic excitations. As a possible reason for the hillocks formation, the plastic deformation due to the defects created by the Coulomb explosion mechanism in the target subsurface layer is suggested.     

Effect of irradiation by 140 Mev Ag ions on the optical and electrical properties of polypropylene/TiO2 composite

Changes in the optical, structural, dielectric properties and surface morphology of a polypropylene/TiO₂ composite due to swift heavy ion irradiation were studied by means of UV–visible spectroscopy, X-ray diffraction, impedance gain phase analyzer and atomic force microscopy. Samples were irradiated with 140 MeV Ag¹¹⁺ ions at fluences of 1 × 10¹¹ and 5 × 10¹² ions/cm². UV–visible absorption analysis reveals a decrease in optical direct band gap from 2.62 to 2.42 eV after a fluence of 5 × 10¹² ions/cm². X-ray diffractograms show an increase in crystallinity of the composite due to irradiation. The dielectric constants obey the Universal law given by ε α f ⁿ⁻¹, where n varies from 0.38 to 0.91. The dielectric constant and loss are observed to change significantly due to irradiation. Cole–cole diagrams have shown the frequency dependence of the complex impedance at different fluences. The average surface roughness of the composite decreases upon irradiation.