硒化铜铟镓太阳电池
钙钛矿(结构)
铟
材料科学
铜
光电子学
太阳能电池
化学
冶金
结晶学
作者
Ivona Kafedjiska,Guillermo A. Farias-Basulto,P. Reyes-Figueroa,Tobias Bertram,Amran Al‐Ashouri,Christian A. Kaufmann,Robert Wenisch,Steve Albrecht,Rutger Schlatmann,Iver Lauermann
标识
DOI:10.1016/j.solmat.2023.112248
摘要
We investigate the performance of monolithic copper-indium-gallium-selenide (CIGS)/perovskite tandem solar cells with two different CIGS bottom device absorbers: Cu(In,Ga)Se2 or Cu(In,Ga)(S,Se)2 and with three different hole-transporting layers (HTLs): NiOx + SAM, NiOx:Cu + SAM and SAM alone. NiOx(:Cu) is (2 wt% copper-doped) nickel oxide and SAM is the MeO-2PACz ([2-(3,6-dimethoxy-9H-carbazol-9-yl)ethyl]phosphonic acid) self-assembled monolayer. The CIGSe is fabricated by physical-vapor deposition (PVD), has a Eg ∼ 1.06eV, and a σRMS,PVD ∼ 65 nm, while the CIGSSe is fabricated by rapid-thermal processing (RTP), has a Eg ∼ 1.01eV, and a σRMS,RTP ∼ 120 nm. While the current certified, 24.2%-efficient, world-record monolithic CIGSe-perovskite tandem solar cell has previously been achieved with SAM as a stand-alone HTL, this work investigates whether SAM can yield similarly high efficiencies also on industrially compatible, very rough RTP CIGSSe absorbers. We find that the devices with SAM as stand-alone HTL suffer from severe FF and Voc losses and that NiOx:Cu is needed to act as a shunt-quenching layer below that SAM, ensuring conformal coverage of the rough bottom sub-cell surface. Within this work the highest-achieved (in-house measured) PCEs for the RTP and PVD CIGS-based tandems are 21.6% and 23.2% respectively, on a cell area of 1.08 cm2, both of which are obtained with NiOx:Cu + SAM as an HTL.
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