Affiliation:
1. Department of Applied Physical Sciences University of North Carolina at Chapel Hill Chapel Hill NC 27599 USA
2. Department of Chemistry University of North Carolina at Chapel Hill Chapel Hill NC 27599 USA
Abstract
AbstractHigh‐performance tin‐lead perovskite solar cells (PSCs) are needed for all‐perovskite‐tandem solar cells. However, iodide related fast photodegradation severely limits the operational stability of Sn‐Pb perovskites despite the demonstrated high efficiency and thermal stability. Herein, this work employs an alkylammonium pseudo‐halogen additive to enhance the power conversion efficiency (PCE) and photostability of methylammonium (MA)‐free, Sn‐Pb PSCs. Density functional theory (DFT) calculations reveal that the pseudo‐halogen tetrafluoroborate (BF4−) has strong binding capacity with metal ions (Sn2+/Pb2+) in the Sn‐Pb perovskite lattice, which lowers iodine vacancy formation. Upon combining BF4− with an octylammonium (OA+) cation, the PCE of the device with a built‐in light‐scattering layer is boosted to 23.7%, which represents a new record for Sn‐Pb PSCs. The improved efficiency benefits from the suppressed defect density. Under continuous 1 sun illumination, the OABF4 embodied PSCs show slower generation of interstitial iodides and iodine, which greatly improves the device photostability under open‐circuit condition. Moreover, the device based on OABF4 retains 88% of the initial PCE for 1000 h under the maximum‐power‐point tracking (MPPT) without cooling.
Funder
U.S. Department of Energy
Office of Energy Efficiency and Renewable Energy
Solar Energy Technologies Office
National Science Foundation
Center for Hybrid Organic Inorganic Semiconductors for Energy
Energy Frontier Research Centers
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment
Cited by
67 articles.
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