Fabrication of copper–indium–gallium–diselenide absorber layer by quaternary-alloy nanoparticles for solar cell applications
► Copper–indium–gallium–diselenide thin films were fabricated using precursor nanoparticle-ink and sintering technology. ► The nanoparticle-ink was fabricated by mixture of CIGS nanoparticles, solution, and organic polymer. ► This device has a conversion efficiency of 2.392%. Copper–indium–gallium–d...
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Veröffentlicht in: | Solar energy 2012-09, Vol.86 (9), p.2795-2801 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | ► Copper–indium–gallium–diselenide thin films were fabricated using precursor nanoparticle-ink and sintering technology. ► The nanoparticle-ink was fabricated by mixture of CIGS nanoparticles, solution, and organic polymer. ► This device has a conversion efficiency of 2.392%.
Copper–indium–gallium–diselenide (CIGS) thin films were fabricated using precursor nanoparticle-ink and sintering technology. The precursor uses quaternary compound composition ratios of Cu/(In+Ga)=0.95, Ga/(In+Ga)=0.39, and Se/(Cu+In+Ga)=0.75, respectively. The nanoparticles were fabricated by a rotary ball milling technique. After milling, the agglomerated CIGS powder to a particle size smaller than 100nm. The nanoparticle-ink was fabricated by mixture of CIGS nanoparticles, solution, and organic polymer. Crystallographic, morphological, stoichiometric, and photovoltaic properties of films were obtained by sintering the precursor CIGS sample in a non-vacuum environment with selenization. Analytical results indicate that the CIGS absorption layer prepared with a nanoparticle-ink polymer, through sintering, has a chalcopyrite structure and favorable compositions. In this sample, the mole ratio of Cu:In:Ga:Se is equal to 0.95:0.69:0.38:1.99, and related ratios of Ga/(In+Ga) and Cu/(In+Ga) are 0.35 and 0.89, respectively. Analysis of a performance of the obtained solar cell under standard air mass 1.5 global illumination revealed a conversion efficiency of 2.392%. |
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ISSN: | 0038-092X 1471-1257 |
DOI: | 10.1016/j.solener.2012.06.018 |