Paper
29 August 2002 Photoemitters based on field and optically induced electron emission
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Proceedings Volume 4905, Materials and Devices for Optical and Wireless Communications; (2002) https://doi.org/10.1117/12.481043
Event: Asia-Pacific Optical and Wireless Communications 2002, 2002, Shanghai, China
Abstract
Electron emission properties of doped In203 and Sn02 (ITO) thin layers have been studied. These layers have been deposited onto both surfaces of a microscope glass using a constant-current ion sputtering method. One of the layer (1 μm thick) was a field electrode and another one (1Onm - 200nm) was treated as an electron emitter. The layers were examined using an electron emission induced by electric field. The polarizing voltage Upol has been applied to the field electrode. The studies has been carried out in vacuum (1O-7 hPa). Electron emission yield dependence on the intensity of an internal field and illumination were measured. The exponential dependence of the pulse frequency n =f(Upol) has been found. With increasing Upol (field strength in a sample) and after illumination the count frequency of pulses grows monotonically. At low Upol (≤|-500V|) the increase is linear. At higher Upol this dependence is exponential. Energy analysis of emitted electrons was performed by the retarding field method. Measurements of electrons energy in field induced emission showed that about 80% of electrons have energy up to 10 eV. It was also found that additional effect at simultaneous emission oftwo electrons as result ofabsorption of a single photon have to be taken into account.
© (2002) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Jadwiga Olesik "Photoemitters based on field and optically induced electron emission", Proc. SPIE 4905, Materials and Devices for Optical and Wireless Communications, (29 August 2002); https://doi.org/10.1117/12.481043
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KEYWORDS
Ionization

Electrodes

Glasses

Semiconductors

Ions

Statistical analysis

Tin

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