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Tin oxide films have been prepared by physical vapor deposition of Sn followed by thermal oxidation and by spray pyrolysis of SnCl 4 or SnCl 4 ·5H 4 O mixed with CH 3 OH. Phase changes and surface morphologies during the syntheses were monitored by X-ray diffraction and scanning electron microscopy. Electrical resistance and UV−visible transmittance of tin oxide films prepared by both methods were measured. The peak shapes of the Auger Sn M 4 N 45 N 45 transition of the prepared tin oxide films were compared to those of commercial SnO and SnO 2 and used to determine rough values of the oxidation state of Sn. Oxygen/tin ratios in the films were determined from analyses of scanning Auger microprobe and X-ray photoelectron spectroscopy and are all less than 2. Auger depth profiles with thermally oxidized tin oxide films on glass substrates show an overlapping region between the tin oxide film and the substrate. These films were tested as sensors for CH 2 Cl 2 in O 2 . The mixed phase (SnO·SnO 2 ) tin oxide films prepared by temperature-programmed thermal oxidation of Sn showed better sensing behavior to CH 2 Cl 2 than single phase (SnO or SnO 2 ) films.
Park et al. (Sat,) studied this question.