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Journal ArticleDOI

Inorganic Rubidium Cation as an Enhancer for Photovoltaic Performance and Moisture Stability of HC(NH2)2PbI3 Perovskite Solar Cells

TLDR
In this paper, the authors proposed an inorganic-organic mixed cation system to enhance moisture-tolerance and photovoltaic performances of formamidinium lead iodide (FAPbI3).
Abstract
Perovskite solar cells (PSCs) based on organic monovalent cation (methylammonium or formamidinium) have shown excellent optoelectronic properties with high efficiencies above 22%, threatening the status of silicon solar cells. However, critical issues of long-term stability have to be solved for commercialization. The severe weakness of the state-of-the-art PSCs against moisture originates mainly from the hygroscopic organic cations. Here, rubidium (Rb) is suggested as a promising candidate for an inorganic–organic mixed cation system to enhance moisture-tolerance and photovoltaic performances of formamidinium lead iodide (FAPbI3). Partial incorporation of Rb in FAPbI3 tunes the tolerance factor and stabilizes the photoactive perovskite structure. Phase conversion from hexagonal yellow FAPbI3 to trigonal black FAPbI3 becomes favored when Rb is introduced. The authors find that the absorbance and fluorescence lifetime of 5% Rb-incorporated FAPbI3 (Rb0.05FA0.95PbI3) are enhanced than bare FAPbI3. Rb0.05FA0.95PbI3-based PSCs exhibit a best power conversion efficiency of 17.16%, which is much higher than that of the FAPbI3 device (13.56%). Moreover, it is demonstrated that the Rb0.05FA0.95PbI3 film shows superior stability against high humidity (85%) and the full device made with the mixed perovskite exhibits remarkable long-term stability under ambient condition without encapsulation, retaining the high performance for 1000 h.

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Citations
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Journal ArticleDOI

In Situ Formation of δ-FAPbI3 at the Perovskite/Carbon Interface for Enhanced Photovoltage of Printable Mesoscopic Perovskite Solar Cells

TL;DR: In this article , a hole-conductor-free triplemesoscopic perovskite solar cells (PSCs) are constructed at the interface between a perov-absorbing layer and charge-transporting layers for enhancing the VOC of PSCs.
Journal ArticleDOI

C60-assisted crystal engineering for perovskite solar cells with enhanced efficiency and stability

TL;DR: In this article, a small amount of fullerene (C60) is added to toluene in the antisolvent dripping process to improve perovskite thin films.
Journal ArticleDOI

Control of the quality and homogeneity of halide perovskites by mixed-chloride additives upon the film formation process

TL;DR: In this article, the effect of ammonium chloride and potassium chloride additives on the formation mechanism of Cs0.1FA0.9PbI3 films upon annealing was highlighted.
Journal ArticleDOI

Beneficial effects of cesium acetate in the sequential deposition method for perovskite solar cells

TL;DR: A small amount of cesium acetate is introduced that can effectively stabilize FAMAPbI3 under thermal- and light illumination-stress and provide insight into how dopants and synthesis precursors play an important role in efficient and stable perovskite solar cells.
References
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Journal ArticleDOI

Organometal Halide Perovskites as Visible-Light Sensitizers for Photovoltaic Cells

TL;DR: Two organolead halide perovskite nanocrystals were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells, which exhibit strong band-gap absorptions as semiconductors.
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Efficient Hybrid Solar Cells Based on Meso-Superstructured Organometal Halide Perovskites

TL;DR: A low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight is reported.
Journal ArticleDOI

Electron-hole diffusion lengths exceeding 1 micrometer in an organometal trihalide perovskite absorber.

TL;DR: In this article, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
Journal Article

Electron-Hole Diffusion Lengths Exceeding 1 Micrometer in an Organometal Trihalide Perovskite Absorber

TL;DR: In this paper, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
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