Electronic structure of pulsed laser deposited carbon thin films monitored by photoluminescence

The influence of pressure of methane atmosphere on the pulsed laser deposited (PLD) amorphous carbon layers (a-C:H) were studied, on the structure on atomic scale as well as on the electronic levels near the band edges. Raman scattering, measured by two different probing wavelengths, show the absenc...

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Bibliographic Details
Published inDiamond and related materials Vol. 12; no. 3; pp. 911 - 916
Main Authors Tóth, S., Caricato, A.P., Füle, M., Veres, M., Koós, M., Pócsik, I.
Format Journal Article Conference Proceeding
LanguageEnglish
Published Amsterdam Elsevier B.V 01.03.2003
Elsevier
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Summary:The influence of pressure of methane atmosphere on the pulsed laser deposited (PLD) amorphous carbon layers (a-C:H) were studied, on the structure on atomic scale as well as on the electronic levels near the band edges. Raman scattering, measured by two different probing wavelengths, show the absence of graphitic ordering of sp 2 hybridized carbons. The samples prepared at low methane pressure are characterized with spectra, similar to the spectra of diamond-like carbon. Infrared absorption of PLD films is dominated in the CH bond stretching region by the bands due to sp 3 CH 3 and sp 3 CH 2 vibrations, however, a weak, widely distributed band also appears over 3000 cm −1. Photoluminescence (PL) can be excited in these samples with decreasing wavelength below 400 nm (over 3.1 eV) and a steep increase of PL intensity occurs below 250 nm (over 4.9 eV). Some distinct PL bands can be distinguished in wavelength region of 270–450 nm (4.6–2.7 eV), the appearance and intensity of which shows correlation with the applied methane pressure.
ISSN:0925-9635
1879-0062
DOI:10.1016/S0925-9635(02)00354-0