Recording and reading of three-dimensional optical memory in glasses

We report on three-dimensional (3D) optical memory recording and reading in glass by femtosecond pulses. Optically induced dielectric breakdown of glass is a mechanism of recording. The formulae of dielectric breakdown presented are applicable, in principle, for any crystalline or amorphous dielectric material. Scaling dependences of the probabilities of multi-photon and impact ionization are given. The measured threshold of an in-bulk dielectric breakdown of silica was reproduced numerically by implementing the ionization potential of Si (8.15 eV) for calculations. Exact measures of focal spot size and pulse duration at the focus allowed us to evaluate the intensity of a pulse during recording of 3D optical memory bits with high accuracy. The readout of the 3D optical memory was carried out by the white-light continuum generated from the previously damaged sites (recorded memory bits). The mechanism of the readout was a four-photon parametric interaction. PACS 42.65.Jx; 42.65.Ky; 42.70.Ce; 42.79.Vb     

Hole drilling in stainless steel and silicon by femtosecond pulses at low pressure

We report on the ablation and hole drilling in stainless steel SUS304 and Si by femtosecond pulses (wavelength 800 nm; pulse duration >80 fs) at the room and low (5 Torr) air pressure ambient. It was found that the quality of surface processing is improved at low pressure avoiding debris formation. The improvement is due to suppression of the conical emission, resulting from the air optical breakdown at a pre-surface area of sample. Debris-free processing of the movable Si-MEMS components is demonstrated. Techniques for the precise measurement of focal spot size and pulse duration are discussed. PACS 87.80.Mj; 78.66.Bz; 42.62.Cf; 61.82.Bg; 61.80.-x     

Influence of ordering change on the optical and thermal properties of inflation polyethylene films

Changes of thermal diffusivity inside femtosecond laser-structured volumes as small as few percent were reliably determined (with standard deviation less than 1%) with miniaturized sensors. An increase of thermal diffusivity of a crystalline high-density polyethylene (HDPE) inflation films by 10-20% from the measured (1.16 ± 0.01) × 10⁻⁷ m² s⁻¹ value in regions not structured by femtosecond laser pulses is considerably larger than that of non-crystalline polymers, 0-3%. The origin of the change of thermal diffusivity are interplay between the laser induced disordering, voids’ formation, compaction, and changes in molecular orientation. It is shown that laser structuring can be used to modify thermal and optical properties. The birefringence and infrared spectroscopy with thermal imaging of CH₂ vibrations are confirming inter-relation between structural, optical, and thermal properties of the laser-structured crystalline HDPE inflation films. Birefringence modulation as high as Δn ∼ ± 1 × 10⁻³ is achieved with grating structures.     

Reduction of capillary force for high-aspect ratio nanofabrication

The wet processing of SU8 resist was modified in order to achieve a high-aspect ratio patterning with feature size of 100 nm. A final rinse in water, which makes a large contact angle on the resist (less wetting) was added to the procedure. This allowed considerable reduction of the capillary force, which is responsible for pattern distortions in three-dimensional (3D) lithography. 3D recording of high-aspect ratio (f_ar=18) structures by holographic exposure using femtosecond pulses in SU8 resist was achieved using this modified development procedure. The thickness of the free-standing planes was approximately 100 nm. High fidelity of this recording method was confirmed by a Moiré pattern transfer into a developed SU8 pattern. In terms of focusing, the 100 nm feature size comprised 1/13-th of the diffraction limit. This modified development is applicable for wet processing when super-critical drying cannot be used. PACS 81.05.-t; 81.07.-b; 81.16.-c; 81.40.-z; 81.65.-b     

Nickel surface anodic oxidation and electrocatalysis of oxygen evolution

The processes of nickel surface anodic oxidation taking place within the range of potentials preceding oxygen evolution reaction (OER) in the solutions of 1 M KOH, 0.5 M K₂SO₄, and 0.5 M H₂SO₄ have been analyzed in the present paper. Metallic nickel, thermally oxidized nickel, and black nickel coating were used as Ni electrodes. The methods of cyclic voltammetry and X-ray photoelectron spectroscopy were employed. The study was undertaken with a view to find the evidence of peroxide-type nickel surface compounds formation in the course of OER on the Ni electrode surface. On the basis of experimental results and literature data, it has been suggested that in alkaline solution at E ≈ 1.5 V (RHE) reversible electrochemical formation of Ni(IV) peroxide takes place according to the reaction as follows: This reaction accounts for both the underpotential (with respect to ) formation of O₂ from NiOO₂ peroxide and also small experimental values of dE/dlgi slope (<60 mV) at low anodic current densities, which are characteristic for the two-electron transfer process. It has been inferred that the composition of the γ-NiOOH phase, indicated in the Bode and revised Pourbaix diagrams, should be ∼5/6 NiOOH + ∼1/6 NiOO₂. The schemes demonstrating potential-dependent transitions between Ni surface oxygen compounds are presented, and the electrocatalytic mechanisms of OER in alkaline, acid, and neutral medium have been proposed.     

Nanoparticle plasmon-assisted two-photon polymerization induced by incoherent excitation source

We demonstrate the possibility to achieve optical triggering of photochemical reactions via two-photon absorption using incoherent light sources. This is accomplished by the use of arrays of gold nanoparticles, specially tailored with high precision to obtain high near-field intensity enhancement.     

Formation of amorphous sapphire by a femtosecond laser pulse induced micro-explosion

We report on structural characterization of void-structures created by a micro-explosion at the locus of a tightly focused femtosecond laser pulse inside the crystalline phase of Al₂O₃ (R3c space group). The transmission electron microscopy (TEM), micro-X-ray diffraction (XRD) analysis, and Raman scattering revealed a presence of strongly structurally modified amorphous regions around the void-structures. We discuss issues of achieving the required resolution for structural characterization and assignment of newly formed phases of nano-crystallites by TEM, XRD, and Raman scattering from micro-volumes of modified materials enclosed inside the bulk of the host phase.     

Warm dense matter at the bench-top: Fs-laser-induced confined micro-explosion

We report the experimental evidence for creation of Warm Dense Matter (WDM) in ultrafast laser-induced micro-explosion inside a sapphire (Al₂O₃) crystal. We show that the WDM can be formed by a 100 nJ fs-pulse if the following conditions are satisfied: (1) the laser pulse is tightly focused to inside of the bulk of transparent material so the intensity at focus is two orders of magnitude higher than the optical breakdown threshold; (2) the pulse duration is shorter than the electron-ion energy exchange time; and, (3) the absorbed energy density is above the Young’s modulus for the material studied. The empty void created inside a sapphire crystal surrounded by a shell of compressed material provides the direct evidence of the maximum pressure above the Young’s modulus of sapphire (∼400 GPa). Synchrotron X-ray diffraction (XRD) analysis of the shell revealed the presence of novel super-dense bcc-Al crystalline phase predicted at pressures above ∼380 GPa theoretically, which has never been observed experimentally before neither in nature in laboratory experiments. These results show that confined micro-explosion induced by tightly focussed fs-laser inside a transparent solid opens new routes for synthesis of new materials and study of WDM at a laboratory bench-top.     

THz photomixer with milled nanoelectrodes on LT-GaAs

A terahertz (THz) photomixer: (i) a meander type antenna with integrated nanoelectrodes on (ii) a low temperature grown GaAs has been fabricated and characterized. It was designed for spectral range of 0.3–0.4 THz where molecular fingerprinting and sensing are performed. By combination of electron beam lithography with post-processing using focused ion beam (FIB), milling the THz emitter was successfully fabricated. Nanogaps as small as 40 nm width in the active area of photomixer were milled by FIB. Nanocontacts enhance electric fields of the illuminated and THz radiation and contribute to a better collection of photo-electrons. THz emission was obtained and spectrally characterized.