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Heterojunction Incorporating Perovskite and Microporous Metal–Organic Framework Nanocrystals for Efficient and Stable Solar Cells
Highlights Microporous indium-based metal–organic framework (In-BTC) nanocrystals are synthesized under an extremely mild condition. Perovskite/In-BTC heterojunction films possess improved morphology/crystallinity and reduced grain boundaries/defects. In-BTC-modified perovskite solar cells exhibit s...
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Published in: | Nano-micro letters 2020-03, Vol.12 (1), p.80-80, Article 80 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Highlights
Microporous indium-based metal–organic framework (In-BTC) nanocrystals are synthesized under an extremely mild condition.
Perovskite/In-BTC heterojunction films possess improved morphology/crystallinity and reduced grain boundaries/defects.
In-BTC-modified perovskite solar cells exhibit significantly enhanced efficiency of 20.87% and long-term stability.
In this paper, we present a facile approach to enhance the efficiency and stability of perovskite solar cells (PSCs) by incorporating perovskite with microporous indium-based metal–organic framework [In
12
O(OH)
16
(H
2
O)
5
(btc)
6
]
n
(In-BTC) nanocrystals and forming heterojunction light-harvesting layer. The interconnected micropores and terminal oxygen sites of In-BTC allow the preferential crystallization of perovskite inside the regular cavities, endowing the derived films with improved morphology/crystallinity and reduced grain boundaries/defects. Consequently, the In-BTC-modified PSC yields enhanced fill factor of 0.79 and power conversion efficiency (PCE) of 20.87%, surpassing the pristine device (0.76 and 19.52%, respectively). More importantly, over 80% of the original PCE is retained after 12 days of exposure to ambient environment (25 °C and relative humidity of ~ 65%) without encapsulation, while only about 35% is left to the pristine device. |
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ISSN: | 2311-6706 2150-5551 |
DOI: | 10.1007/s40820-020-00417-1 |