Quasi-single scattering of low-energy Ne ions from the Fe3O4 surfaces

The energy spectra of positive and negative ions emitted from single-crystalline Fe₃O₄ (0 0 1) and (1 1 1) surfaces under low-energy Ne⁺ ion bombardments were investigated in the temperature range from 85 to 300 K. The characteristics of the LEIS spectra of the two surfaces are very similar. The positive-charged-ion spectra have revealed the O⁺-recoil and the quasi-single scattering Ne⁺-Fe peak, while a large broad O⁻¹ recoil signal was observed in the negative-charged-ion ones. No change of the peak shape and of the energy position have revealed for the (0 0 1) surface, whereas the (1 1 1) one implies an appearance of a small peak around 150 K attributed to recoil-oxygen ions from the double-collisions.     

Irradiation effects on solid surfaces by water cluster ion beams

The interaction between a water cluster ion beam and the surface of a silicon substrate was investigated. The sputtering yield of silicon by a water cluster ion beam was approximately ten times larger than that by an argon monomer ion beam. X-ray photoelectron spectroscopy was used to analyze the silicon surface irradiated with a water cluster ion beam. The analysis revealed that the surface was oxidized, and the oxidation was saturated approximately at the dose of 1 × 10¹⁴ ions/cm². The number of disordered atoms measured by the Rutherford backscattering also supported the result.     

Growth, spectroscopic properties and laser performance of Nd-doped potassium ytterbium tungstate laser crystal

The 5 at.% Nd³⁺-doped potassium ytterbium tungstate (Nd³⁺:KYb(WO₄)₂, hereafter Nd:KYbW) laser crystal with the dimension up to 28 mm × 15 mm × 12 mm was grown by the top seeded solution growth (TSSG) method. The infrared spectrum of crystal sample was measured, and the vibrational peaks were assigned. According to the absorption and emission spectra of crystal sample, the absorption and emission cross-sections are 16.03 × 10⁻²⁰ cm² at 808 nm and 10.72 × 10⁻²⁰ cm² at 1067 nm, respectively. The fluorescence life of ⁴F_3/2 energy level is 196.33 μs, and the fluorescence branching ratio for the ⁴F_3/2-⁴I_11/2 transition at 1067 nm is 55.74%. The energy transfer between Nd³⁺ and Yb³⁺ ions was observed from the fluorescence spectra pumped by 808 and 980 nm LD sources and the Stark levels of Yb³⁺ in Nd:KYbW crystal were determined. Highly efficient laser output up to 305 mW of Nd:KYbW crystal at 1067 nm has been achieved under pumping by a CW 808 nm laser diode at room temperature. The optical-optical conversion efficiency is 33.9% and the slope efficiency is 46.8%.     

Electron spectroscopy (UPS(HeI and II) and metastable impact electron spectroscopy (MIES)) applied to molecular surfaces: the interaction of atoms and molecules with solid water

We report studies of the interaction of atoms and molecules with solid molecular surfaces, water in particular, by combining photoelectron spectroscopy, UPS with HeI and II, and metastable impact electron spectroscopy (MIES). In MIES charge exchange processes of the Auger-type taking place between metastable He atoms and the surface under study are utilized to gain information on their electronic structure. The MIES spectra give a rather direct image of the surface DOS. We concentrate on the following processes taking place on water films produced at 80 K:(1) Interaction of Na Atoms with Amorphous Solid H₂O Films: emphasis was on the role of the 3sNa electrons in the water dissociation process. In order to make a detailed comparison with density functional theory (DFT), DOS (density of states) information is compared with the MIES spectra. Our results are consistent with the theoretical prediction that the 3s-electron is delocalized from the Na-core and trapped (solvated) between the Na-core and water molecules of the surrounding water shell.(2) Ionization and Solvation of NaCl Interacting with Amorphous Solid Water: at 90 K there is no interpenetration of H₂O and NaCl. However, ionic dissociation of NaCl takes place when H₂O and NaCl are in direct contact. At 105 K the solvation of the ionic species Cl⁻ and Na⁺ becomes significant. The desorption of H₂O from the mixed film takes place between 145 and 170 K; those species bound ionically to Na⁺ and Cl⁻ are removed last.(3) The Interaction of PBTs (persistent, bio-accumulative, and toxic substances), chlorobenzene and chlorophenyl, with amorphous solid water: the organic layers produced at 80 K were annealed up to 200 K under in situ control of MIES and UPS. The different behaviour of the interfaces for the three studied cases is traced back to the different mobilities of the molecules with respect to that of water. The interaction between H₂O and the benzene derivatives is discussed on the basis of qualitative free energy profiles.     

Development and application of highly charged ion source

The interaction of slow highly charged ions (HCIs) with solid surfaces is useful for ‘nanoprocess’; the modification, activation, machining and analysis in nanometer scale. An electron beam ion source ‘Kobe EBIS’ has been developed for the application of HCIs to nanoprocesses. The ion source produces ion beams of Ar^q+ (q ≤ 12) HCI in the nanoampere range. The ion source was applied to irradiate samples in order to investigate the structural or electric modification effect of HCIs with high fluence on the topmost layers of sample surfaces.     

Influence of texture on optical and electrical properties of diamond films

The optical and electrical properties of variously textured diamond films have been investigated in this paper. SEM and Raman spectrum indicated that the films produced were of high quality with either (0 0 1) or (1 1 1) orientation. A four-layer model was used to fit the measured spectroscopic ellipsometry data. The results indicated that the properties of (0 0 1)-oriented diamond films were superior to those of (1 1 1)-oriented one. The refractive index and extinction coefficient of (0 0 1)-oriented diamond film in the infrared region of 2500-12500 nm was measured as 2.391 and of the order of 10⁻⁵, respectively and that for (1 1 1)-oriented one was 2.375 and of the order of 10⁻⁴, respectively. The dark current of the (0 0 1)-oriented diamond film was measured as 33.7 nA for an applied electric field of 100 kV cm⁻¹, its resistivity being about 2.33×10¹⁰ Ω cm. Current passing through the (0 0 1)-oriented diamond film during testing did not change significantly.     

‘The crystal structure problem’ in noble gas nanoclusters

Calculations of the energetics of multiply twinned particles (MTPs) such as icosahedra and decahedra with fivefold symmetry as well as face-centered cubic (fcc) and hexagonal close-packed (hcp) particles in the size interval from 13 up to ∼ 45,000 atoms were made applying Lennard-Jones potentials. We essentially extended the size interval comparatively with previous studies and included shape-optimized hcp clusters in the global energy analysis that gives rise to the new insight into the basic fcc/hcp problem. For the cluster size N from minimal up to N ∼ 2000 atoms the binding energy is highest for icosahedra, in the size interval from 2000 up to ∼ 11,500 atoms decahedra prevail, above N ∼ 11,500 atoms decahedra and optimized fcc clusters were found to alternate. The hcp structure was revealed to become favorable above N ∼ 34,000 atoms. Thus, hcp clusters can attain their preference with respect to MTPs (comprising fcc fragments) and optimized fcc clusters only for very large sizes. The comparison with several other models is suggested and the opportunity of experimental observations is discussed.     

Effect of swift heavy ion irradiation on bare and coated ZnS quantum dots

The present study compares structural and optical modifications of bare and silica (SiO₂) coated ZnS quantum dots under swift heavy ion (SHI) irradiation. Bare and silica coated ZnS quantum dots were prepared following an inexpensive chemical route using polyvinyl alcohol (PVA) as the dielectric host matrix. X-ray diffraction (XRD) and transmission electron microscopy (TEM) study of the samples show the formation of almost spherical ZnS quantum dots. The UV-Vis absorption spectra reveal blue shift relative to bulk material in absorption energy while photoluminescence (PL) spectra suggests that surface state and near band edge emissions are dominating in case of bare and coated samples, respectively. Swift heavy ion irradiation of the samples was carried out with 160 MeV Ni¹²⁺ ion beam with fluences 10¹² to 10¹³ ions/cm². Size enhancement of bare quantum dots after irradiation has been indicated in XRD and TEM analysis of the samples which has also been supported by optical absorption spectra. However similar investigations on irradiated coated quantum dots revealed little change in quantum dot size and emission. The present study thus shows that the coated ZnS quantum dots are stable upon SHI irradiation compared to the bare one.     

Structural and optical properties of polycrystalline CdSexTe1−x (0 ≤ x ≤ 0.4) thin films

CdSe_xTe_1−x (0 ≤ x ≤ 0.4) ternary thin films have been deposited on quartz substrates at room temperature by a single source thermal evaporation. X-ray diffraction patterns and transmission electron microscope micrographs of these films showed that the films were of polycrystalline texture over the whole range studied and exhibit predominant cubic (zinc blende) structure with strong preferential orientation of the crystallites along (1 1 1) direction. Linear variation of the lattice constant with mole fraction x is observed obeying Vegard's law. The dependence of the optical constants, the refractive index n and extinction coefficient k, of the films on the mole fraction x was studied in the spectral range of 400-2500 nm. The normal dispersion of the refractive index of the films could be described using the Wemple-DiDomenco single-oscillator model. CdSe_xTe_1−x thin films of different composition have two direct and indirect transitions corresponding to energy gaps and . The variation in either or with x indicates that this system belongs to the amalgamation type. The variation follows a subquadratic dependence and the bowing parameters were found to be 0.36 and 0.48 eV for the direct, and indirect energy gaps, respectively. Direct linear variation of the ratio N/m^* with x is observed.     

Study on field emission and photoluminescence properties of ZnO/graphene hybrids grown on Si substrates

Zinc oxide/graphene (ZnO/G) hybrids are prepared on n-Si (1 0 0) substrates by electrophoretic deposition and magnetron sputtering technique. The crystal structure, morphology and photoluminescence (PL) properties of the ZnO/G hybrids are analyzed via X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM) and fluorescence–phosphorescence spectrometer, respectively. The results indicate that the crystal quality of ZnO nanostructure deteriorates after depositing graphene buffer layer. Whereas many three dimensional stacking blowballs form in the ZnO/G hybrid, creating a larger surface area than that of ZnO nanostructure. The photoluminescence (PL) spectrum of the ZnO/G hybrid contains multi-peaks, which are consistent with ZnO nanostructure except for two new peaks at 390 and 618 nm. In addition, field emission measurement reveals that E_to and E_thr decrease from 8.01 V μm⁻¹ and 14.90 V μm⁻¹ of the ZnO nanostructure to 2.72 V μm⁻¹ and 7.70 V μm⁻¹ of the ZnO/G hybrid. ZnO/G hybrid is characteristic of having excellent emitting behavior suitable for application in field emission technology.     

Mechanical,thermal and laser damage threshold analyses of II group metal complexes of thiourea

Single crystals of thiourea metal complexes with selected Group II metal ions, Zinc and Cadmium, have been grown by solvent evaporation technique. The crystals grown are bisthiourea zinc chloride (BTZC) and bisthiourea cadmium chloride (BTCC). Following an improved photopyroelectric technique, the thermal transport properties have been determined. It is found that BTCC has a higher heat capacity (304.09 J kg⁻¹ K⁻¹) than BTZC (255.24 J kg⁻¹ K⁻¹), and hence BTCC has better thermal stability. Vicker's microhardness measurements reveal that these materials have reverse indentation size effect and belong to the category of soft materials. Elastic stiffness is found to be higher for BTCC (1.57 GPa) than BTZC (0.76 GPa). The roles of the Group II metal ions in improving the mechanical and thermal stability of the metal complexes are discussed. Multi-shot laser damage studies on these materials reveal that BTCC has a higher laser damage threshold (15 GW cm⁻²) than BTZC (6 GW cm⁻²).     

Epitaxial growth of transparent tin oxide films on (0 0 0 1) sapphire by pulsed laser deposition

The growth of epitaxial SnO₂ on (0 0 0 1) sapphire using pulsed laser deposition is examined. X-ray diffraction analysis shows that the films are highly a-axis oriented SnO₂ with the rutile structure. Three distinct symmetry-equivalent in-plane epitaxial orientations were observed between the film and substrate. With increasing growth temperature, both the growth rate and surface roughness increase with columnar grain formation. Carrier concentration ranged from 10¹⁷ to 10¹⁹ cm⁻³, with mobility of 0.5-3 cm²/V s. The resistivity of the films increases with increasing growth temperature, suggesting a lower density of oxygen vacancy-related defects formed during high temperature deposition.     

Effect of Titanium ion implantation on the oxidation behaviour of zircalloy-4 at 500 °C

The beneficial effect of titanium ion implantation on the oxidation behaviour of zircalloy-4 at 500 °C was investigated. Titanium ions were implanted by a MEVVA source at an energy of 40 keV with dose 5×10¹⁶, 1×10¹⁷, and 2×10¹⁷ ion/cm² at the maximum temperature 130 °C. Weight gain curves of the as-received and implanted zircalloy-4 were measured after oxidation in air at 500 °C for 100 min. It was found that improvement was achieved in the oxidation behaviour of titanium ion implanted samples compared with that of the as-received one. The valence of the oxides in the scale was analyzed by X-ray photoemission spectroscopy. Glancing angle X-ray diffraction was used to examine the phase transformation in the oxide films and is showed that the addition of titanium transformed the phase from monoclinic zirconia to hexagonal zirconia. Finally, the mechanism of improvements oxidation behaviour is discussed.     

Vertically aligned Mn-doped zinc oxide nanorods by hybrid wet chemical route

Mn-doped zinc oxide (Mn:ZnO) nanorods were synthesized by incorporating manganese in aligned ZnO nanorods. For this, Mn was evaporated onto ZnO nanorods and the composite structure was subjected to rapid thermal annealing. The nanorods were preferentially oriented in (0 0 2) direction as indicated by the XRD measurement. Optical band gap was seen to decrease with increasing amount of Mn incorporation. XPS studies indicated that incorporated Mn was in Mn²⁺ and Mn⁴⁺ states. Mn²⁺ atomic concentration was found to be larger than Mn⁴⁺ concentration in all the samples. The Raman spectra of the Mn:ZnO nanorods indicated the presence of the characteristic peak at ∼438 cm⁻¹ for high frequency branch of E₂ mode of ZnO. The PL peak at ∼376 nm (∼3.29 eV) was ascribed to the band edge luminescence while the peak at ∼394 nm (∼3.15 eV) was assigned to the donor bound exciton (D^oX) and free exciton transition related to Mn²⁺ states.     

Enhancement of mechanical and tribological properties in AISI D3 steel substrates by using a non-isostructural CrN/AlN multilayer coating

Enhancement of mechanical and tribological properties on AISI D3 steel surfaces coated with CrN/AlN multilayer systems deposited in various bilayer periods (Λ) via magnetron sputtering has been studied in this work exhaustively. The coatings were characterized in terms of structural, chemical, morphological, mechanical and tribological properties by X-ray diffraction (XRD), electron dispersive spectrograph, atomic force microscopy, scanning and transmission electron microscopy, nanoindentation, pin-on-disc and scratch tests. The failure mode mechanisms were observed via optical microscopy. Results from X-ray diffraction analysis revealed that the crystal structure of CrN/AlN multilayer coatings has a NaCl-type lattice structure and hexagonal structure (wurtzite-type) for CrN and AlN, respectively, i.e., made was non-isostructural multilayers. An enhancement of both hardness and elastic modulus up to 28 GPa and 280 GPa, respectively, was observed as the bilayer periods (Λ) in the coatings were decreased. The sample with a bilayer period (Λ) of 60 nm and bilayer number n  =  50 showed the lowest friction coefficient (∼0.18) and the highest critical load (43 N), corresponding to 2.2 and 1.6 times better than those values for the coating deposited with n = 1, respectively. The best behavior was obtained when the bilayer period (Λ) is 60 nm (n = 50), giving the highest hardness 28 GPa and elastic modulus of 280 GPa, the lowest friction coefficient (∼0.18) and the highest critical load of 43 N. These results indicate an enhancement of mechanical, tribological and adhesion properties, comparing to the CrN/AlN multilayer systems with 1 bilayer at 28%, 21%, 40%, and 30%, respectively. This enhancement in hardness and toughness for multilayer coatings could be attributed to the different mechanisms for layer formation with nanometric thickness such as the Hall–Petch effect and the number of interfaces that act as obstacles for the crack deflection and dissipation of crack energy.     

Substrate temperature dependence of the properties of Ga-doped ZnO films deposited by DC reactive magnetron sputtering

Ga-doped zinc oxide (ZnO:Ga) transparent conductive films were deposited on glass substrates by DC reactive magnetron sputtering. The influence of substrate temperature on the structural, electrical, and optical properties of ZnO:Ga films was investigated. The X-ray diffraction (XRD) studies show that higher temperature helps to promote Ga substitution more easily. The film deposited at 350 °C has the optimal crystal quality. The morphology of the films is strongly related to the substrate temperature. The film deposited is dense and flat with a columnar structure in the cross-section morphology. The transmittance of the ZnO:Ga thin films is over 90%. The lowest resistivity of the ZnO:Ga film is 4.48×10⁻⁴ Ω cm, for a film which was deposited at the substrate temperature of 300 °C.     

Synthesis, characterization and effect of low energy Ar ion irradiation on gadolinium oxide nanoparticles

In this work, we report on the surfactant assisted synthesis of gadolinium oxide (Gd₂O₃) nanoparticles and their characterization through various microscopic and spectroscopic tools. Exhibiting a monoclinic phase, the nanoscale Gd₂O₃ particles are believed to be comprising of crystallites with an average size of ∼3.2 nm, as revealed from the X-ray diffraction analysis. The transmission electron microscopy has predicted a particle size of ∼9 nm and an interplanar spacing of ∼0.28 nm. Fourier transform infrared spectroscopy studies show that Gd-O inplane vibrations at 536.8 and 413.3 cm⁻¹ were more prominent for 80-keV Ar-ion irradiated Gd₂O₃ nanosystem than unirradiated system. The photoluminescence (PL) spectra of irradiated specimen have revealed an improvement in the symmetry factor owing to significant enhancement of surface-trap emission, compared to the band-edge counterpart. Irradiation induced creation of point defects (oxygen vacancies) were predicted both from PL and electron paramagnetic resonance (EPR) studies. Further, the Raman spectra of the irradiated sample have exhibited notable vibrational features along with the evolution of a new peak at ∼202 cm⁻¹. This can be ascribed to an additional Raman active vibrational response owing to considerable modification of the nanostructure surface as a result of ion bombardment. Probing nanoscale defects through prime spectroscopy tools would find a new avenue for precise tuning of physical properties with generation and annihilation of defects.     

Crystal structure and characterization of a novel organic optical crystal: 2-Aminopyridinium trichloroacetate

2-Aminopyridinium trichloroacetate, a novel organic optical material has been synthesized and crystals were grown from aqueous solution employing the technique of controlled evaporation. 2-Aminopyridinium trichloroacetate crystallizes in monoclinic system with space group P2₁/c and the lattice parameters are a = 8.598(5) Å, b = 11.336(2) Å, c = 11.023(2) Å, β = 102.83(1)° and volume = 1047.5(3) Å³. High-resolution X-ray diffraction measurements were performed to analyze the structural perfection of the grown crystals. Thermal analysis shows a sharp endothermic peak at 124 °C due to melting reaction of 2-aminopyridinium trichloroacetate. UV-vis-NIR studies reveal that 2-aminopyridinium trichloroacetate has UV cutoff wavelength at 354 nm. Dielectric studies show that dielectric constant and dielectric loss decreases with increasing frequency and finally it becomes almost a constant at higher frequencies for all temperatures. The negative nonlinear optical parameters of 2-aminopyridinium trichloroacetate were derived by the Z-scan technique.     

Photoluminescence and field-emission characteristics of ZnO nanowires synthesized by two-step method

ZnO nanowires with excellent photoluminescence (PL) and field-emission properties were synthesized by a two-step method, and the ZnO nanowires grew along (0 0 2) direction. PL measurements showed that the ZnO nanowires have stronger ultraviolet emission properties at 376 nm and there is 3 nm blue shift after the nanowires were immersed in thiourea (TU) solution compared with those of without immersion. The immersed-ZnO nanowires show a turn-on field of 2.3 V/μm at a current density of 0.1 μA/cm and emission current density up to 1 mA/cm² at an applied field of 6.8 V/μm, which demonstrate that the immersed-ZnO nanowires posses efficient field-emission properties in contrast with those not immersed. The ZnO nanowires may be ideal candidates for making luminescent devices and field-emission displays.     

Optical properties of Pb nanowires on Si(3 3 5)

Pb films and self-assembled nanowires on Si(3 3 5) grown at temperature equal to 265 K are investigated by optical reflectance method and scanning tunneling microscopy. In the optical studies s-polarized light with the photon energy from 0.35 to 2.0 eV was used. The measurements were performed during the Pb deposition, for two orientations of the sample: with the light electric field along, and perpendicularly to the Pb nanowires. Two thickness ranges were distinguished: first, for the coverages less than 2 ML, and second, for the larger coverages. The large anisotropy in the optical reflectance was observed in the second range of the thicknesses. The anisotropy was caused by the presence of self-assembled, parallelly aligned metallic nanowires. For the two orthogonal orientations of the sample the reflectance ratio as high as 3.8 was observed.