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Oriented Perovskite Crystal towards Efficient Charge Transport in FASnI3 Perovskite Solar Cells
Despite a higher power conversion efficiency (PCE) than other lead‐free perovskite solar cells (PSCs) due to intrinsically excellent optoelectronic properties and suitable bandgaps of tin (Sn) perovskites, Sn‐based PSCs still suffer from issues of stability and efficiency for practical applications....
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Published in: | Solar RRL 2020-10, Vol.4 (10), p.n/a |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Despite a higher power conversion efficiency (PCE) than other lead‐free perovskite solar cells (PSCs) due to intrinsically excellent optoelectronic properties and suitable bandgaps of tin (Sn) perovskites, Sn‐based PSCs still suffer from issues of stability and efficiency for practical applications. Herein, a novel strategy of tuning perovskite crystal orientation toward ≈45° with respect to the substrate by doping 2,3‐diaminopropionic acid monohydrochloride (2,3‐DAPAC) into formamidinium tin iodide (FASnI3) is proposed, which facilitates charge transport in the perovskite film and consequent device performances. In addition, the incorporation of 2,3‐DAPAC into FASnI3 enables dense and smooth high‐quality perovskite films with less Sn vacancies. Applications of the 2,3‐DAPAC‐treated FASnI3 films into PSCs acquire a champion PCE of 7.23%, showing 37.2% enhancement compared with 5.27% of the control device. Moreover, the storage stabilities of both perovskite films and PSCs are significantly prolonged with improved film quality.
A novel strategy of tuning perovskite crystal orientation toward ≈45° inclination with respect to the substrate is proposed with incorporating 2,3‐diaminopropionic acid monohydrochloride (2,3‐DAPAC) into FASnI3, which facilitates charge transport in the perovskite film from bottom to top. The solar cells with 2,3‐DAPAC acquire a champion power conversion efficiency of 7.23% and improved stability. |
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ISSN: | 2367-198X 2367-198X |
DOI: | 10.1002/solr.202000153 |