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although at present their efficiencies and lifetimes are lower than for crystalline
                     products. Research into thin film and other potentially low cost solar cell materials
                     may see these technologies dominate the solar cell market over coming decades.

                     2.2.4  Thin film crystalline silicon
                     A very wide range of methods are being investigated to develop thin film silicon cells
                     deposited on foreign substrates (Green, 2003). If the ratio of hydrogen to silane in the
                     gas from which amorphous silicon is deposited is increased, the resulting material
                     becomes microcrystalline, with columns of crystallites separated by amorphous
                     regions. The optical and electronic properties are similar to those of bulk silicon.
                     Such material has been used as an alternative to silicon-germanium alloys in hybrid
                     structures with amorphous silicon. Particular measures are necessary to allow the
                     amorphous layers to be kept thin enough to avoid light-induced degradation while
                     producing similar current to the microcrystalline cell(s) in series. A microcrystalline/
                     amorphous tandem design has been developed with an efficiency of about 11% on a
                     laboratory scale.
                     One company is approaching commercial production with a process in which a thin
                     film silicon cell is formed on a textured glass superstrate. A laser is used to form
                     craters through the active material to contact the n-type layer closest to the glass. Low
                     quality material is deposited, then improved by subsequent thermal steps.

                     2.3    ABSORPTION OF LIGHT

                     When light falls onto semiconductor material, photons with energy (E ph ) less than the
                     bandgap energy (E g ) interact only weakly with the semiconductor, passing through it
                     as if it were transparent. However, photons with energy greater than the bandgap
                     energy (E ph  > E g ) interact with electrons in covalent bonds, using up their energy to
                     break bonds and create electron-hole pairs, which can then wander off independently.
                     This is illustrated in Fig. 2.6.




















                            Figure 2.6. The creation of electron-hole pairs when illuminated with light of
                            energy E ph = hf, where E ph > E g.

                     Higher energy photons are absorbed closer to the surface of the semiconductor than
                     lower energy photons, as illustrated in Fig. 2.7.




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