CdTe nanocrystals sequestered and passivated in an amorphous TiO 2 thin film matrix have been prepared by RF sputtering from a composite TiO 2 :CdTe target. The CdTe nanocrystal size and volume fraction increases from 15 to 40 nm and 2 to 20% respectively as the film thickness increases, typically from 0.05 to 0.25 µm. A systematic dependence of the optical band edge on the CdTe nanocrystal size shows a strong quantum confinement effect. The optical edge shifts are significantly higher than the theoretical prediction based on single-particle confinement of decoupled electrons and holes. This is understood on the basis of nucleation-controlled growth of CdTe nanocrystals by direct vapour phase condensation, in which small nuclei are rapidly passivated by TiO 2 depositing at much higher rates. The nano-sized CdTe growth island thus formed comprises of several TiO 2 passivated nanocrystals. Electrical conduction behaviour of these films show that tunnelling between the CdTe nanocrystals is not a dominant mechanism, as a three-dimensional network is not realized due to small thickness and lower coverage. The current transport is essentially space-charge-limited. The injection of electrons from nano-sized CdTe crystals follows spherical radial space charge flow which modifies the usual power law dependence from quadratic to 3/2. The analytical description of the current conduction process in composite CdTe:TiO 2 is discussed.
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Rastogi et al. (2000) studied this question.
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