Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 4, Issue 46, Pages 17939-17945Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ta07712a
Keywords
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Funding
- National Science Foundation [DMR-1608279]
- Office of Naval Research [N00014-14-1-0246]
- Asian Office of Aerospace RD [FA2386-15-1-4106]
- Department of Energy SunShot [DE-EE0006710]
- Boeing-Johnson Foundation
- China Scholarship Council
- State of Washington through the University of Washington Clean Energy Institute
- Direct For Mathematical & Physical Scien
- Division Of Materials Research [1608279] Funding Source: National Science Foundation
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Partially replacing Pb with Sn in organic-inorganic lead halide perovskites has been proven as a promising approach to reduce environmental toxicity and develop low bandgap (as low as 1.20 eV) perovskite solar cells (PVSCs) beneficial for constructing perovskite-based tandem solar cells. In this work, we demonstrated that partially replacing MA(+) or FA(+) with Cs+ in a Pb-Sn binary perovskite system can effectively retard the associated crystallization rate to facilitate homogenous film formation, subsequently resulting in enhanced device performance and stability, especially for high Sn-containing compositions. The representative MA(0.9)Cs(0.1)Pb(0.5)Sn(0.5)I(3) PVSC with a low E-g of 1.28 eV not only achieves an improved efficiency up to 10.07% but also possesses much improved thermal and ambient stability as compared to the pristine MAPb(0.5)Sn(0.5)I(3) PVSC showing poorer efficiency (6.36%) and stability. Similarly, when Cs was introduced into FAPb(1-x)Sn(x)I(3) perovskite, enhanced performance was observed, affirming its general applicability and beneficial role in mediating the crystal growth and film formation of Pb-Sn binary perovskites.
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