Multi‐Functional MoO 3 Doping of Carbon‐Nanotube Top Electrodes for Highly Transparent and Efficient Semi‐Transparent Perovskite Solar Cells
MoO 3 doping of carbon‐nanotube top electrodes in perovskite solar cells is multi‐functional and facilitates p‐doping, favorable energy‐level alignment, and enhanced hole transport. The optimal layer thickness of MoO 3 (8 nm) is determined for decreasing the sheet resistance of carbon‐nanotube elect...
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Veröffentlicht in: | Advanced materials interfaces 2022-04, Vol.9 (11) |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | MoO
3
doping of carbon‐nanotube top electrodes in perovskite solar cells is multi‐functional and facilitates p‐doping, favorable energy‐level alignment, and enhanced hole transport. The optimal layer thickness of MoO
3
(8 nm) is determined for decreasing the sheet resistance of carbon‐nanotube electrodes without damaging the perovskite film. The sheet resistance decreases by approximately one‐third from its original value, which is a substantially better result than that previously reported for acid doping of carbon‐nanotube top electrodes. MoO
3
deposition lowers the Fermi level of the carbon‐nanotube electrode, improving its energy‐level alignment and hole‐transfer performance. When coated with 2,2′,7,7′‐tetrakis[N,N‐di(4‐methoxyphenyl)amino]‐9,9′‐spirobifluorene (spiro‐MeOTAD), MoO
3
crystallizes on the carbon nanotubes and further enhances hole collection. Semi‐transparent perovskite solar cells with MoO
3
‐doped carbon‐nanotube electrodes have a power conversion efficiency of 17.3% with a transmittance of approximately 60% (at a wavelength of 1000 nm). Because of their favorable transparency in the infrared region, these perovskite solar cells are evaluated for use in a tandem structure with silicon solar cells via computational simulations. The predicted device efficiency (23.7%) exceeds that of conventional indium‐tin‐oxide‐based tandem solar cells (23.0%). |
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ISSN: | 2196-7350 2196-7350 |
DOI: | 10.1002/admi.202101595 |