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Dimensional Engineering of a Graded 3D–2D Halide Perovskite Interface Enables Ultrahigh Voc Enhanced Stability in the p‐i‐n Photovoltaics
2D halide perovskite materials have shown great advantages in terms of stability when applied in a photovoltaic device. However, the impediment of charge transport within the layered structure drags down the device performance. Here for the first time, a 3D–2D (MAPbI3‐PEA2Pb2I4) graded perovskite in...
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Published in: | Advanced energy materials 2017-10, Vol.7 (20), p.n/a |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | 2D halide perovskite materials have shown great advantages in terms of stability when applied in a photovoltaic device. However, the impediment of charge transport within the layered structure drags down the device performance. Here for the first time, a 3D–2D (MAPbI3‐PEA2Pb2I4) graded perovskite interface is demonstrated with synergistic advantages. In addition to the significantly improved ambient stability, this graded combination modifies the interface energy level in such a way that reduces interface charge recombination, leading to an ultrahigh Voc at 1.17 V, a record for NiO‐based p‐i‐n photovoltaic devices. Moreover, benefiting from the graded structure induced continuously upshifts energy level, the photovoltaic device attains a high Jsc of 21.80 mA cm−2 and a high fill factor of 0.78, resulting in an overall power conversion efficiency (PCE) of 19.89%. More importantly, it is showed that such a graded interface structure also suppresses ion migration in the device, accounting for its significantly enhanced thermal stability.
A designer cross‐dimensional perovskite–perovskite (3D–2D) interface upshifts the energy level toward the surface, pronouncedly reduces the charge recombination in perovskite photovoltaics, leading to a record high VOC at 1.17 V. Strongly enhanced ambient and thermal stability is also demonstrated. |
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ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.201701038 |