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Enhancing photomultiplication (PM) in organic photodetectors (OPDs) requires effective control of photogenerated trapped electrons. Conventional approaches typically adjust the conduction band of the acceptor. In this study, we present a novel strategy for precisely controlling electron trapping and trapped carrier lifetime in PM-OPDs. We synthesized a series of nonfullerene acceptors (NFAs) by modifying the ratio of conducting and insulating components in the conjugated molecular structure. By enhancing the insulating properties of the NFAs, we slowed both electron trapping and de-trapping processes. This resulted in fine-tuned trapped carrier lifetime (280-581 ms), trapped carrier density (2.04-13.4 × 10 cm), and Schottky barrier height (0.334-0.229 eV) under illumination. Higher concentrations of trapped electrons accumulated at the P3HT/Al interface, leading to a thinner Schottky barrier, reduced depletion region, and enhanced band bending, improving hole injection from the cathode. Among the NFAs, A-BTP-DT, with the highest insulating properties, exhibited superior PM effects, achieving a maximum external quantum efficiency of 7520% at -10 V (compared to 564% for the Y6-based device). This work represents the first successful demonstration of fine-tuning of electron trapping and PM effects, not by adjusting energy levels, but by modifying the insulating properties.
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http://dx.doi.org/10.1039/d5mh00640f | DOI Listing |
Nanotechnology
September 2025
China University of Petroleum Beijing, No.18, Fuxue Road, Changping District, Beijing 102249, China, Changping, Beijing, 102249, CHINA.
In fluid catalytic cracking (FCC) processes, vanadium is a primary harmful feedstock contaminant that deactivates catalysts by forming vanadate species which corrode the zeolite framework and damage catalyst structure. Introducing vanadium capture agents is an effective way to enhance the catalytic performance, but the mechanism of the interaction has not yet been fully understood. This study demonstrates that lanthanum-based additives significantly improve vanadium resistance in FCC catalysts.
View Article and Find Full Text PDFInorg Chem
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, China.
Photocatalysis has emerged as a promising strategy to address water pollution caused by heavy metals and antibiotics. Zeolites exhibit significant potential in petrochemical catalysis; however, the development of zeolite-based photocatalysts remains a critical challenge for researchers. Herein, a novel Z-scheme heterojunction was designed and fabricated on the titanium-silicon zeolite TS-1 by modifying g-CN via a simple calcination process.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Soft Matter Sciences and Engineering, CNRS, École supérieure de Physique et de Chimie Industrielles de la Ville de Paris, Université Paris Sciences et Lettres, Sorbonne Université, Paris 75005, France.
The sliding motion of aqueous droplets on hydrophobic surfaces leads to charge separation at the trailing edge, with implications from triple-line friction to hydrovoltaic energy generation. Charges deposited on the solid surface have been attributed to ions or electrons ripped off from the liquid drop. However, the dynamics and exact physicochemical nature of these surface-trapped charges remains poorly explored.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Kathleen Lonsdale Materials Chemistry, Department of Chemistry, University College London, London WC1H 0AJ, U.K.
The exceptional performance of ceria (CeO) in catalysis and energy conversion is fundamentally governed by its defect chemistry, particularly oxygen vacancies. The formation of each oxygen vacancy (V) is assumed to be compensated by two localized electrons on cations (Ce). Here, we show by combining theory with experiment that while this 1 V: 2Ce ratio accounts for the global charge compensation, it does not apply at the local scale, particularly in nanoparticles.
View Article and Find Full Text PDFJ Chem Phys
September 2025
Quantum Chemistry Division, Yokohama City University, Seto 22-2, Kanazawa-Ku, Yokohama 236-0027, Kanagawa, Japan.
Perovskite-silicon tandem solar cells have attracted considerable attention owing to their high power conversion efficiency (PCE), which exceeds the limits of single-junction devices. This study focused on lead-free tin-based perovskites with iodine-bromine mixed anions. Bromide perovskites have a wide bandgap; therefore, they are promising light absorbers for perovskite-silicon tandem solar cells.
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