Optimized carrier extraction at interfaces for 23.6% efficient tin-lead perovskite solar cells

Carrier extraction in mixed tin-lead perovskite solar cells is improved by modifying the top and bottom perovskite surfaces with ethylenediammonium diiodide and glycine hydrochloride, respectively. Trap densities in perovskite layers are reduced as a result of surface passivation effects and an incr...

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Published inEnergy & environmental science Vol. 15; no. 5; pp. 296 - 217
Main Authors Hu, Shuaifeng, Otsuka, Kento, Murdey, Richard, Nakamura, Tomoya, Truong, Minh Anh, Yamada, Takumi, Handa, Taketo, Matsuda, Kazuhiro, Nakano, Kyohei, Sato, Atsushi, Marumoto, Kazuhiro, Tajima, Keisuke, Kanemitsu, Yoshihiko, Wakamiya, Atsushi
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 18.05.2022
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Summary:Carrier extraction in mixed tin-lead perovskite solar cells is improved by modifying the top and bottom perovskite surfaces with ethylenediammonium diiodide and glycine hydrochloride, respectively. Trap densities in perovskite layers are reduced as a result of surface passivation effects and an increase in film crystallinity. In addition, the oriented aggregation of the ethylenediammonium and glycinium cations at the charge collection interfaces results in the formation of surface dipoles, which facilitate charge extraction. As a result, the treated mixed tin-lead perovskite solar cells showed improved performance, with a fill factor of 0.82 and a power conversion efficiency of up to 23.6%. The unencapsulated device also shows improved stability under AM1.5 G, retaining over 80% of the initial efficiency after 200 h continuous operation in an inert atmosphere. Our strategy is also successfully applied to centimeter-scale devices, with efficiencies of up to 21.0%. This work provides an efficient way to facilitate both electron and hole extraction in the designated interfaces of perovskite solar cells. A record power conversion efficiency of 23.6% for mixed Sn-Pb perovskite solar cell devices is realized.
Bibliography:https://doi.org/10.1039/d2ee00288d
Electronic supplementary information (ESI) available. See DOI
ISSN:1754-5692
1754-5706
DOI:10.1039/d2ee00288d