Ternary CuGaSe2 Research Articles

A comparative study of the effects of light and heavy alkali-halide postdeposition treatment on CuGaSe2 and Cu(In,Ga)Se2 thin-film solar cells

Enhancement of photovoltaic performance due to alkali-metal doping in various thin-film compound solar cells such as chalcogenide Cu(In,Ga)Se2 (CIGS), Cu2ZnSnS4 (CZTS), and organic–inorganic hybrid perovskite, is significant in the development of photovoltaic technologies. In this work, the effects of light Li- and heavy Cs-doping in ternary CuGaSe2 (CGS) and quaternary CIGS thin-films and devices are compared. The new findings are: (i) heavy alkali-metal halide CsF postdeposition treatment (PDT) modifies the CGS film surface morphology and increases the carrier density; however, the beneficial effects of Cs on the CGS photovoltaic performance are low when compared to the results observed from quaternary CIGS devices; (ii) LiF-PDT leads to no significant CGS and CIGS film surface (hetero p-n junction interface) modifications; thus, the use of a thin (approximately 30 nm) CdS buffer layer is not effective in enhancing photovoltaic performance; and (iii) the beneficial effects of either light Li or heavy Cs on ternary CGS devices are modest; nonetheless, Li may be more effective than Cs, unlike quaternary CIGS devices.

Interfacial alkali diffusion control in chalcopyrite thin-film solar cells.

Alkali elements, specifically sodium (Na), are key materials to enhance the energy conversion efficiencies of chalcopyrite and related thin-film photovoltaic solar cells. Recently, the effect of potassium (K) has also attracted attention because elemental K has unique effects different from Na as well as a similar beneficial effect in improving device performance. In this study, the control of selective alkali K and Na diffusion into chalcopyrite thin-films from soda-lime glass substrates, which serve as the monolithic alkali source material and contain both K and Na, is demonstrated using ternary CuGaSe2. Elemental K is found to be incorporated in the several ten nanometer thick Cu-deficient region, which is formed on the CuGaSe2 film surface, while Na is ejected, although both K and Na diffuse from the substrate to the CuGaSe2 film surface during growth. The alkali [K]/[Na] concentration ratio in the surface region of CuGaSe2 films strongly depends on the film structure and can be controlled by growth parameters under the same substrate temperature conditions. The results we present here offer new concepts necessary to explore and develop emerging new chalcopyrite and related materials and optimize their applications.