Metal halide perovskites with bandgap of ≈1.8 eV are competitive candidates for indoor photovoltaic (IPV) devices, owing to their superior photovoltaic properties and ideal absorption spectra matched to most indoor light sources. However, these perovskite IPVs suffer from severe trap induced non-radiative recombination, resulting in large open-circuit voltage (V) losses, particularly under low light intensity. Herein, an effective approach is developed to minimizing trap density by modifying the buried interface of perovskite layer with bifunctional molecular 2-(4-Fluorophenyl)ethylamine Hydrobromide (F-PEABr). The benzene ring of F-PEABr molecules can firmly anchor at the hole transporting layer by π-π stacking interaction, and the other ends can passivate the defects on the buried interface of perovskite layer. Based on that, the F-PEABr modified perovskite IPVs achieved power conversion efficiency (PCE) of 42.3% with a remarkable V of 1.13 V under 1000 lux illumination from a 4000 K LED lamp. Finally, perovskite IPV mini-modules with area of 10.40 cm are demonstrated with a PCE of 35.2%. This interface modification strategy paves the way for crafting high-performance perovskite IPVs, holding great potential for self-powered internet of things applications.
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http://dx.doi.org/10.1002/smll.202408271 | DOI Listing |
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November 2024
Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, and Laboratory of Advanced Materials, Fudan University, Shanghai, 200438, P. R. China.
Metal halide perovskites with bandgap of ≈1.8 eV are competitive candidates for indoor photovoltaic (IPV) devices, owing to their superior photovoltaic properties and ideal absorption spectra matched to most indoor light sources. However, these perovskite IPVs suffer from severe trap induced non-radiative recombination, resulting in large open-circuit voltage (V) losses, particularly under low light intensity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2024
Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
The lanthanide contraction involves a reduction in atomic radius among f-block elements below the expected level. A similar contraction is observed in group-16 elements. The atomic radius of Se (117 pm) is slightly larger than that of S (104 pm) arising from the presence of d electrons, compared to the significant increase in atomic radius from O (73 pm) to S.
View Article and Find Full Text PDFAdv Mater
September 2024
School of Optoelectronics, Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China.
The rapid development of the Internet of Things (IoT) has accelerated the advancement of indoor photovoltaics (IPVs) that directly power wireless IoT devices. The interest in lead-free perovskites for IPVs stems from their similar optoelectronic properties to high-performance lead halide perovskites, but without concerns about toxic lead leakage in indoor environments. However, currently prevalent lead-free perovskite IPVs, especially tin halide perovskites (THPs), still exhibit inferior performance, arising from their uncontrollable crystallization.
View Article and Find Full Text PDFChem Commun (Camb)
July 2023
Hybrid Solar Cells, Faculty of Engineering and Natural Sciences, Tampere University, P.O. Box 541, FI-33014, Tampere, Finland.
Are lead-free perovskite-inspired materials (PIMs) the wise choice for efficient yet sustainable indoor light harvesting? This feature article outlines how wide-bandgap PIMs can provide a positive answer to this compelling question. The wide band gaps can hinder sunlight absorption, in turn limiting the solar cell performance. However, PIMs based on group VA of the periodic table can theoretically lead to an outstanding indoor power conversion efficiency up to 60% when their band gap is ∼2 eV.
View Article and Find Full Text PDFAdv Mater
August 2023
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, Suzhou, 215123, P. R. China.
Metal halide perovskites are ideal candidates for indoor photovoltaics (IPVs) because of their easy-to-adjust bandgaps, which can be designed to cover the spectrum of any artificial light source. However, the serious non-radiative carrier recombination under low light illumination restrains the application of perovskite-based IPVs (PIPVs). Herein, polar molecules of amino naphthalene sulfonates are employed to functionalize the TiO substrate, anchoring the CsPbI perovskite crystal grains with a strong ion-dipole interaction between the molecule-level polar interlayer and the ionic perovskite film.
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