Alkalis are essential in Cu(In,Ga)Se2 absorber layers for efficient solar cells. Current doping methods rely on solid state diffusion of an alkali through to the absorber layer, e.g. a thin NaF layer on Mo or NaCl dissolved in a metal precursor ink[1]. The apparent concentration of alkali in the final absorber is determined by the initial alkali dosing and the use of an interfacial barrier to stop alkali diffusion from the substrate. Until now the vapor–absorber interface as a source or sink of alkali doping has been largely ignored. We show that device efficiency improves from 2 to 8% by gas phase Na adsorption alone. Conversely initial results show that Na can also be desorbed to the gas phase. Although these efficiencies are lower than those obtained by including Na directly in the precursor (device efficiency 13.3% [1]), the findings are relevant to all chalcogenide growers as they show that exact doping, and thus control of device efficiency, is only possible when gas phase adsorption/desorption processes are controlled.

On the Role of Vapour Phase Alkali Species for Efficient Cu(In,Ga)Se2 Solar Cells

D. Colombara;
2015

Abstract

Alkalis are essential in Cu(In,Ga)Se2 absorber layers for efficient solar cells. Current doping methods rely on solid state diffusion of an alkali through to the absorber layer, e.g. a thin NaF layer on Mo or NaCl dissolved in a metal precursor ink[1]. The apparent concentration of alkali in the final absorber is determined by the initial alkali dosing and the use of an interfacial barrier to stop alkali diffusion from the substrate. Until now the vapor–absorber interface as a source or sink of alkali doping has been largely ignored. We show that device efficiency improves from 2 to 8% by gas phase Na adsorption alone. Conversely initial results show that Na can also be desorbed to the gas phase. Although these efficiencies are lower than those obtained by including Na directly in the precursor (device efficiency 13.3% [1]), the findings are relevant to all chalcogenide growers as they show that exact doping, and thus control of device efficiency, is only possible when gas phase adsorption/desorption processes are controlled.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11567/1066151
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