Organic hole-transporting materials for 9.32%-efficiency and stable CsPbBr 3 perovskite solar cells
Cost-effective and stable CsPbBr 3 -based inorganic perovskite solar cells (PSCs) are regarded as promising candidates for next-generation photovoltaics. However, the large interfacial energy differences at the CsPbBr 3 /hole-transporting layer lead to serious charge recombination and poor charge ex...
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Veröffentlicht in: | Materials chemistry frontiers 2018-11, Vol.2 (12), p.2239-2244 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Cost-effective and stable CsPbBr 3 -based inorganic perovskite solar cells (PSCs) are regarded as promising candidates for next-generation photovoltaics. However, the large interfacial energy differences at the CsPbBr 3 /hole-transporting layer lead to serious charge recombination and poor charge extraction kinetics. Herein, we prepare a series of hole-transporting materials (HTMs) to improve hole extraction and to reduce electron–hole recombination at the CsPbBr 3 /HTM interface. In comparison with the power conversion efficiency (PCE) of 6.10% for an HTM-free device, the CsPbBr 3 PSCs with polymeric HTMs such as polythiophene, polypyrrole and polyaniline yield efficiencies of 8.36%, 8.32% and 7.69%, respectively. Similarly, the inorganic PSC with organic small molecule BT-BTH achieves a PCE as high as 9.32% due to the improved hole conductivity. Moreover, the unencapsulated PSC with BT-BTH maintains 94% of its initial efficiency in 70% relative humidity over 80 days. |
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ISSN: | 2052-1537 2052-1537 |
DOI: | 10.1039/C8QM00337H |