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This work reports upon the dilution effect of Ar + H2 on the microstructures, optical, and photovoltaic properties of the hydrogenated nanocrystalline silicon (nc-Si:H) thin films. High crystallinity (up to 82.6%) nc-Si:H thin films were fabricated from silane diluted by Ar + H2 in a low-frequency inductively coupled plasma (LFICP) facility at a low temperature of 300 °C. The substitution of H2 by Ar in the diluent gas leads to an increase of the deposition rate, grain size, and crystallinity, and a decrease of the optical bandgap. Varying the Ar content caused a fluctuation of the H concentration and a change of the preferential orientation from (111) to (220) in the synthesized thin films. These effects physically originated from changes of the Ar + H2 + SiH4 plasma environment in the LFICP system. The enhancement of the dissociation of SiH4/H2 molecules by ion Ar+ and the metastable state Ar* were discussed in terms of related chemical reactions between the diluent gases and silane. Furthermore, it was found that a heterojunction solar cell prototype based on the as-deposited nc-Si:H thin films exhibits an excellent photovoltaic response.
Nano-crystalline Si/SiO 2 multilayers were prepared by alternately changing the ultra-thin amorphous Si film deposition and the in situ plasma oxidation process followed by the post-annealing treatments. Well-defined periodic structures can be achieved with 2.5 nm thick SiO 2 sublayers. It is shown that the size of formed nano-crystalline Si is about 3 nm. Room temperature electroluminescence can be observed and the spectrum contains two luminescence bands located at 650 nm and 520 nm. In order to improve the hole injection probability, p-i-n structures containing a nanocrystalline Si/SiO 2 luminescent layer were designed and fabricated on different p-type substrates. It is found that the turn-on voltage of p-i-n structures is obviously reduced and the luminescence intensity increases by 50 times. It is demonstrated that the use of a heavy-doped p-type substrate can increase the luminescence intensity more efficiently compared with the light-doped p-type substrate due to the enhanced hole injection.
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