UV‐Inert ZnTiO3 Electron Selective Layer for Photostable Perovskite Solar Cells

Although planar‐structured perovskite solar cells (PSCs) have power conversion efficiencies exceeding 24%, the poor photostability, especially with ultraviolet irradiance (UV) severely limits commercial application. The most commonly‐used TiO2 electron selective layer has a strong photocatalytic eff...

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Veröffentlicht in:Advanced energy materials 2019-10, Vol.9 (40), p.n/a
Hauptverfasser: Wei, Jing, Guo, Fengwan, Liu, Bing, Sun, Xiangyu, Wang, Xi, Yang, Zijiang, Xu, Kun, Lei, Ming, Zhao, Yicheng, Xu, Dongsheng
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Sprache:eng
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Zusammenfassung:Although planar‐structured perovskite solar cells (PSCs) have power conversion efficiencies exceeding 24%, the poor photostability, especially with ultraviolet irradiance (UV) severely limits commercial application. The most commonly‐used TiO2 electron selective layer has a strong photocatalytic effect on perovskite/TiO2 interface when TiO2 is excited by UV light. Here a UV‐inert ZnTiO3 is reported as the electron selective layer in planar PSCs. ZnTiO3 is a perovskite‐structured semiconductor with excellent chemical stability and poor photocatalysis. Solar cells are fabricated with a structure of indium doped tin oxide (ITO)/ZnTiO3/Cs0.05FA0.81MA0.14PbI2.55Br0.45/Sprio‐MeOTAD/Au. The champion device exhibits a stabilized power conversion efficiency of 19.8% with improved photostability. The device holds 90% of its initial efficiency after 100 h of UV soaking (365 nm, 8 mW cm−2), compared with 55% for TiO2‐based devices. This work provides a new class of electron selective materials with excellent UV stability in perovskite solar cell applications. A UV‐inert ZnTiO3 is demonstrated to be an electron selective layer in perovskite solar cells. ZnTiO3 is a perovskite‐structured semiconductor with excellent chemical stability and poor photocatalysis. Planar perovskite solar cells based on ZnTiO3 exhibit power conversion efficiency of 20.1% with improved photostability. The best device holds 90% of its initial efficiency after 100 h of ultraviolet soaking.
ISSN:1614-6832
1614-6840
DOI:10.1002/aenm.201901620