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The scanning electron microscope (SEM) is a powerful tool for analyzing the surface of various specimens. SEM observation at low voltage, which is typically lower than the 1 kV range, is very effective for obtaining surface information of specimens. However, at the low voltage range, resolution is restricted by the brightness and energy spread of electron sources. Therefore, to improve the resolution, a bright and monochromatic electron source is indispensable. In this work, we focused on an electron gun with a negative electron affinity photocathode using p-type GaAs and Cs–O adsorbates. The resolution of a prototype SEM was improved by approximately 16% compared with a SEM using a conventional Schottky emission (SE)-type emitter at the acceleration voltage of 1 kV. In addition, results showed that the measured brightness was as high as an SE-type emitter (∼107 A/m2/sr/V) and the estimated energy spread was less than 0.2 eV, which was narrower than that of a cold field emission-type emitter. [ABSTRACT FROM AUTHOR]

A pulsed gas electron diffraction apparatus was developed and applied to investigate an alignment process of molecules in intense laser fields. A two-dimensional (2D) electron diffraction pattern of jet-cooled CS[SUB2] in intense nanosecond laser fields)(1064 nm, ∼0.64 TW/cm[SUP2], 10 ns) was measured using short-pulsed 25 keV electron beam packets (∼7 ns) generated by irradiating a tantalum photocathode with the 4th harmonics of pulsed YAG laser light. The observed anisotropic 2D diffraction pattern was analyzed quantitatively by taking into account the spatio-temporal distributions of the laser pulses, the electron beam packets, and the molecular beam through a numerical simulation of the observed diffraction pattern. The anisotropy of the spatial distribution of molecular axes of CS[SUB2] in the laser polarization direction is accounted for by the effect of the intense laser fields. Considering the spatio-temporal averaging effect, the temporal pulse width of an electron packet required for real-time probing of the alignment process of molecules in intense nanosecond laser fields is discussed. A numerical simulation of temporal and spatial profiles of an electron packet is also performed to examine conditions for generating sub-picosecond ultrashort electron pulse for real-time probing of ultrafast molecular dynamics by the pulsed gas electron diffraction method. [ABSTRACT FROM AUTHOR]