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Modifying perovskites with functional additives has proven effective in refining the crystallization process and passivating the defects of perovskite films, thereby ensuring high photovoltaic efficiencies. However, conventional methods that involve pre-mixing additives into the precursor solution often face challenges due to discrepancies in the spatial distribution of slow-diffused additives relative to dynamically formed defect sites, resulting in limited passivation effectiveness. To address this issue, this study innovatively proposes a dynamic passivation strategy that utilizes a pre-passivator to gradually release active additives during the thermal crystallization process of perovskite films. By leveraging the principle of energy minimization, these timely-released additives can interact precisely and selectively with the high-energy defect sites generated during crystallization, thus facilitating efficient additive utilization and in situ real-time defect passivation. Through analysis of crystallization kinetics and carrier dynamic, it is demonstrated that this dynamic passivation approach significantly improves film quality and prolongs carrier lifetime, outperforming traditional pre-mixing tactics. Consequently, the final perovskite solar cell achieves an impressive solar conversion efficiency of 25.33 %, along with exceptional stability. This work provides strong support of tailored additive strategies aimed at further enhancing the efficiency of perovskite solar cells and their subsequent commercial applications.
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http://dx.doi.org/10.1002/anie.202421637 | 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 PDFAnal Chem
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, P. R. China.
Rational design of both mechanistic pathways and material compositions is essential to advance COF-based electrochemiluminescence (ECL) systems. In this study, aggregation-induced emission covalent organic framework (AIE-COF) nanoprobes with excellent ECL performance were developed based on Tb-functionalized covalent organic framework (Tb@A-COF). The Tb@A-COF system demonstrates enhanced ECL performance through synergistic integration of three complementary mechanisms: (1) (4',4',4',4'-(1,2-ethenediylidene)tetrakis [1,1'-biphenyl]-4-carboxaldehyde (ETBC) ligands function as antenna-like sensitizers that amplify luminescence intensity by 14.
View Article and Find Full Text PDFSmall
September 2025
Shenzhen Key Laboratory of Intelligent Robotics and Flexible Manufacturing Systems, Department of Mechanical and Energy Engineering, SUSTech Energy Institute for Carbon Neutrality, Southern University of Science and Technology, Shenzhen, 518055, China.
The surface passivation with phenethylammonium halides has proven effective in reducing defect density and trap-assisted recombination, enabling outstanding efficiency in perovskite solar cells. Despite its promise, it is ambiguous whether this strategy can improve the stability of devices under rigorous conditions, such as light soaking and thermal aging. A critical issue is whether the interface is robust in structure and morphology under light illumination.
View Article and Find Full Text PDFNanomicro Lett
September 2025
School of Microelectronics, Northwestern Polytechnical University, Xi'an, 710129, People's Republic of China.
Metal halide perovskites (MHPs) with striking electrical and optical properties have appeared at the forefront of semiconductor materials for photocatalytic redox reactions but still suffer from some intrinsic drawbacks such as inferior stability, severe charge-carrier recombination, and limited active sites. Heterojunctions have recently been widely constructed to improve light absorption, passivate surface for enhanced stability, and promote charge-carrier dynamics of MHPs. However, little attention has been paid to the review of MHPs-based heterojunctions for photocatalytic redox reactions.
View Article and Find Full Text PDFSmall
September 2025
Faculty of Electronics, Telecommunications, and Informatics, Gdansk University of Technology, 11/12 G. Narutowicza Str., Gdansk, 80-233, Poland.
Two-dimensional black phosphorus (BP or phosphorene) has drawn significant interest in alkali metal ion storage due to its capacity to adsorb alkali atoms and high theoretical prediction of specific capacity. But the problem persists in large-scale production of the nanoscale BP, low electronic conductivity, considerable volume change (≈300%), and polyphosphide-induced shuttle effect. To solve this problem, a single-step lasing method is employed to prepare nanoscale BP covalently bound to the sp2 bonded carbon framework through a P─O─C/P─C bond.
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