[신간의 별자리x] 우리/미술, 그리고 ‘슬픔의 박물관’

The application of electrostatic lenses is demonstrated to give a substantial improvement of the two-dimensional (2D) ion/electron imaging technique. This combination of ion lens optics and 2D detection makes “velocity map imaging” possible, i.e., all particles with the same initial velocity vector are mapped onto the same point on the detector. Whereas the more common application of grid electrodes leads to transmission reduction, severe trajectory deflections and blurring due to the non-point source geometry, these problems are avoided with open lens electrodes. A three-plate assembly with aperture electrodes has been tested and its properties are compared with those of grid electrodes. The photodissociation processes occurring in molecular oxygen following the two-photon 3dπ(3Σ1g −)(v=2, N=2)←X(3Σg −) Rydberg excitation around 225 nm are presented here to show the improvement in spatial resolution in the ion and electron images. Simulated trajectory calculations show good agreement with experiment and ...

Velocity map imaging of ions and electrons using electrostatic lenses: Application in photoelectron and photofragment ion imaging of molecular oxygen

Summary form only given. Fundamental processes in atoms, molecules, as well as condensed matter are triggered or mediated by the motion of electrons inside or between atoms. Electronic dynamics on atomic length scales tends to unfold within tens to thousands of attoseconds (1 attosecond [as] = 10-18 s). Recent breakthroughs in laser science are now opening the door to watching and controlling these hitherto inaccessible microscopic dynamics. The key to accessing the attosecond time domain is the control of the electric field of (visible) light, which varies its strength and direction within less than a femtosecond (1 femtosecond = 1000 attoseconds). Atoms exposed to a few oscillations cycles of intense laser light are able to emit a single extreme ultraviolet (XUV) burst lasting less than one femtosecond. Full control of the evolution of the electromagnetic field in laser pulses comprising a few wave cycles have recently allowed the reproducible generation and measurement of isolated sub-femtosecond XUV pulses, demonstrating the control of microscopic processes (electron motion and photon emission) on an attosecond time scale. These tools have enabled us to visualize the oscillating electric field of visible light with an attosecond "oscilloscope", to control single-electron and probe multi-electron dynamics in atoms, molecules and solids. Recent experiments hold promise for the development of an attosecond X-ray source, which may pave the way towards 4D electron imaging with sub-atomic resolution in space and time.

Attosecond Physics

Plasma–liquid interactions represent a growing interdisciplinary area of research involving plasma science, fluid dynamics, heat and mass transfer, photolysis, multiphase chemistry and aerosol science. This review provides an assessment of the state-of-the-art of this multidisciplinary area and identifies the key research challenges. The developments in diagnostics, modeling and further extensions of cross section and reaction rate databases that are necessary to address these challenges are discussed. The review focusses on non-equilibrium plasmas.

/pdf/plasma-liquid-interactions-a-review-and-roadmap-4kfoerpjnh.pdf

Plasma-liquid interactions: A review and roadmap

This self-contained, comprehensive book describes the fundamental properties of soft x-rays and extreme ultraviolet (EUV) radiation and discusses their applications in a wide variety of fields, including EUV lithography for semiconductor chip manufacture and soft x-ray biomicroscopy. The author begins by presenting the relevant basic principles such as radiation and scattering, wave propagation, diffraction, and coherence. He then goes on to examine a broad range of phenomena and applications. The topics covered include EUV lithography, biomicroscopy, spectromicroscopy, EUV astronomy, synchrotron radiation, and soft x-ray lasers. He also provides a great deal of useful reference material such as electron binding energies, characteristic emission lines and photo-absorption cross-sections. The book will be of great interest to graduate students and researchers in engineering, physics, chemistry, and the life sciences. It will also appeal to practicing engineers involved in semiconductor fabrication and materials science.

X-Rays and Extreme Ultraviolet Radiation: Principles and Applications

Femtosecond time-resolved photoelectron imaging (TRPEI) is a variant of time-resolved photoelectron spectroscopy used in the study of gas-phase photoinduced dynamics. A new observable, time-dependent photoionization-differential cross section provides useful information on wave-packet motions, electronic dephasing, and photoionization dynamics. This review describes fundamental issues and the most recent works involving TRPEI.

Femtosecond time-resolved photoelectron imaging.

Generation of sub-two-cycle, microjoule pulses in the mid-infrared region is demonstrated. Fundamental and second-harmonic pulses of 25 fs Ti:sapphire amplifier output were focused into the air to produce extremely broadband mid-infrared pulses by four-wave difference-frequency generation through the filamentation. The full width at half-maximum of the spectral bandwidth reaches one octave (2.5-5.5 microm), which is sufficiently broad for sub-single-cycle pulse generation. The pulse width was estimated to be 13 fs, without any compressors, by cross-correlation frequency resolved optical gating. The output energy of more than a few microjoule is sufficient for spectroscopy.

Generation of sub-two-cycle mid-infrared pulses by four-wave mixing through filamentation in air.

We present the first measurement of the vertical binding energy (VBE) of a hydrated electron in bulk water by the time-resolved photoelectron spectroscopy (TRPES) of the charge-transfer-to-solvent (CTTS) reaction in aqueous NaI solution. Our best estimate of VBE is 3.27 +/- 0.10 eV for H(2)O and 3.20 +/- 0.10 eV for D(2)O.

Direct measurement of vertical binding energy of a hydrated electron

Generation of deep-ultraviolet femtosecond pulses by four-wave mixing through filamentation in neon gas was demonstrated Fundamental (ω) and second-harmonic (2ω) pulses of 25 fs Ti:sapphire amplifier output were focused into neon gas, and 20 μJ pulses with the center wavelength of 260 nm were produced by a four-wave mixing process, 2ω+2ω−ω→3ω through an ∼15 cm filament Additionally, pulses with an energy of 2 μJ at 200 nm were generated, probably by a cascaded process, 3ω+2ω−ω→4ω The 260 nm pulses were compressed by a grating-based compressor and characterized by a dispersion-free transient grating frequency-resolved optical gating The estimated pulse width was 12 fs

Toshinori Suzuki

Papers

Femtosecond time-resolved photoelectron imaging.

Generation of sub-two-cycle mid-infrared pulses by four-wave mixing through filamentation in air.

Direct measurement of vertical binding energy of a hydrated electron

Generation of 12 fs deep-ultraviolet pulses by four-wave mixing through filamentation in neon gas.

Nonadiabatic dynamics within the time dependent density functional theory: Ultrafast photodynamics in pyrazine