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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 |
J Phys Chem Lett
September 2025
Department of Materials Science and Engineering, Dankook University, Cheonan 31116, Korea.
Inorganic halide perovskites are promising light absorbers due to their thermal stability, high absorption, and tunable optoelectronic properties. CsPbIBr, with a suitable bandgap and robust phase stability, is particularly attractive for indoor photovoltaics (IPVs). However, achieving uniform, defect-minimized films remains challenging.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Hybrid Solar Cells, Faculty of Engineering and Natural Sciences, Tampere University, Tampere FI-33014, Finland.
Efficient surface passivation is crucial for mitigating defect-induced recombination losses in perovskite-based indoor photovoltaics (IPVs), where charge carrier dynamics are particularly sensitive to trap states under low-intensity illumination. Here, we introduce two pyridine-based passivators, tris[4-(pyridin-4-yl)phenyl]amine () and its ionic counterpart (), to achieve high-performance and stable perovskite IPVs. These passivators strongly coordinate with under-coordinated Pb ions, effectively reducing trap densities and improving hydrophobicity.
View Article and Find Full Text PDFACS Energy Lett
July 2025
Hybrid Solar Cells, Faculty of Engineering and Natural Sciences, Tampere University, P.O. Box 541, Tampere, FI-33014, Finland.
Perovskite-inspired materials (PIMs) are promising candidates for low-toxicity indoor photovoltaics (IPVs), but their power conversion efficiencies (PCEs) have been so far largely limited by poor thin-film morphology and suboptimal device architectures. Here, we report a PCE exceeding 10% under 1000 lux indoor lighting by integrating device and film engineering strategies, including a dual-purpose interfacial modifier atop a hybrid antimony-bismuth halide PIM, advancing the development of efficient pnictogen-based IPVs for Internet of Things (IoT) applications.
View Article and Find Full Text PDFSmall
August 2025
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, P. R. China.
Perovskite-based indoor photovoltaics (IPVs) have emerged as competitive candidates for low-power consumption electronic devices, where the development of fully solution-processed fabrication protocols becomes urgent to enable roll-to-roll compatible manufacture. In this study, blade-coated perovskite IPV devices are developed by blade-coating high-quality hole and electron transporting layers through solvent and morphology engineering, respectively. A uniform hole-transporting layer of polymeric carbazole phosphonic acid is achieved by tuning the properties co-solvent system, while a compact electron-transporting layer of poly(fullerene-alt-xylene) is realized by adjusting the morphology of the underlying perovskite layer.
View Article and Find Full Text PDFAdv Mater
April 2025
Department of Applied Physics, Research Center for Organic Electronics, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, 999077, P. R. China.
Wide-bandgap (WBG) perovskite solar cells (PSCs) have garnered considerable attention of late for their potential as semitransparent photovoltaics for building integration, top-cells in tandem configurations, and indoor photovoltaics (IPVs) for Internet of Things (IoT) applications. However, recent investigations have unveiled that underlying defect-mediated phase segregation, ion migration, lattice strain, and other factors can give rise to self-accelerated degradation reactions and the contraction of quasi-Fermi level splitting (QFLS) within devices. Extensive efforts have been undertaken to reduce defect densities in bulks, at surfaces, and across interfaces with charge transport layers (CTLs).
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