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Journal ArticleDOI

Molecular Interaction Regulates the Performance and Longevity of Defect Passivation for Metal Halide Perovskite Solar Cells

TLDR
It is unraveled that the passivation agents with a stronger interaction energy are advantageous not only for effective defect passivation but also to suppress defect migration.
Abstract
Defect passivation constitutes one of the most commonly used strategies to fabricate highly efficient perovskite solar cells (PSCs). However, the durability of the passivation effects under harsh operational conditions has not been extensively studied regardless of the weak and vulnerable secondary bonding between the molecular passivation agents and perovskite crystals. Here, we incorporated strategically designed passivating agents to investigate the effect of their interaction energies on the perovskite crystals and correlated these with the performance and longevity of the passivation effects. We unraveled that the passivation agents with a stronger interaction energy are advantageous not only for effective defect passivation but also to suppress defect migration. The prototypical PSCs treated with the optimal passivation agent exhibited superior performance and operational stability, retaining 81.9 and 85.3% of their initial performance under continuous illumination or nitrogen at 85 °C after 1008 h, respectively, while the reference device completely degraded during that time. This work provides important insights into designing operationally durable defect passivation agents for perovskite optoelectronic devices.

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Citations
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Journal ArticleDOI

Multifunctional Chemical Bridge and Defect Passivation for Highly Efficient Inverted Perovskite Solar Cells

TL;DR: In this article, the interfacial recombination at the perovskite/hole conductor interface generally results in significant energy losses in inverted perov-skite solar cells (PSCs) with a p-i-n device architecture.
Journal ArticleDOI

Chlorobenzenesulfonic Potassium Salts as the Efficient Multifunctional Passivator for the Buried Interface in Regular Perovskite Solar Cells

TL;DR: In this paper , chlorobenzenesulfonic potassium (3Cl−BSAK) is used to modify the buried tin oxide (SnO2)/perovskite interface for regular PSCs.
Journal ArticleDOI

Passivating buried interface via self-assembled novel sulfonium salt toward stable and efficient perovskite solar cells

TL;DR: In this article, a simple and effective buried interface passivation strategy based on cation engineering through employing a new type of sulfonium salt ((2-carboxyethyl) dimethyl sulfonoium chloride, CDSC) together with reference molecule (3-dimethylamino propionic acid hydrochloride, DPAH) to modify the interface between perovskite and electron transport layers.
Journal ArticleDOI

Passivating buried interface via self-assembled novel sulfonium salt toward stable and efficient perovskite solar cells

TL;DR: In this article , a simple and effective buried interface passivation strategy based on cation engineering through employing a new type of sulfonium salt ((2-carboxyethyl) dimethyl sulfonoium chloride, CDSC) together with reference molecule (3-dimethylamino propionic acid hydrochloride, DPAH) to modify the interface between perovskite and electron transport layers.
References
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Journal ArticleDOI

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.
Journal ArticleDOI

Long-Range Balanced Electron- and Hole-Transport Lengths in Organic-Inorganic CH3NH3PbI3

TL;DR: Two studies show, using a variety of time-resolved absorption and emission spectroscopic techniques, that perovskite materials manifest relatively long diffusion paths for charge carriers energized by light absorption, highlighting effective carrier diffusion as a fruitful parameter for further optimization.
Journal ArticleDOI

Iodide management in formamidinium-lead-halide–based perovskite layers for efficient solar cells

TL;DR: The introduction of additional iodide ions into the organic cation solution, which is used to form the perovskite layers through an intramolecular exchanging process, decreases the concentration of deep-level defects, enabling the fabrication of PSCs with a certified power conversion efficiency.
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