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Addressing the critical challenges of interfacial defects and insufficient stability in perovskite solar cells, this work introduces a co-solvent engineering strategy to dynamically regulate the phenethylammonium chloride (PEACl) passivation layer. The effect of isopropyl alcohol (IPA) and a DMSO: IPA (1:100) mixture as solvent for forming the PEACl 2D passivation layer is systematically explored, and the synergistic interplay between solvent coordination strength and crystallization kinetics is systematically investigated. The DMSO: IPA (1:100) blend balances Pb-O coordination (via DMSO) and rapid phase separation (via IPA), enabling the oriented growth of a dense, ultrathin 2D perovskite overlayer. This suppresses defect density (electron traps reduced to 1.68 × 10 cm) and extends carrier lifetime, yielding a champion power conversion efficiency (PCE) of 24.27%-a significant improvement over the control (22.73%). For the first time, we establish a dual-parameter "solvent coordination-crystallization kinetics" model, providing a universal framework for designing environmentally benign solvent systems and advancing the industrial scalability of high-performance perovskite solar cells (PSCs).
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http://dx.doi.org/10.3390/nano15090699 | DOI Listing |
Nanomaterials (Basel)
May 2025
The College of New Materials and New Energies, Shenzhen Technology University, Lantian Road 3002, Pingshan, Shenzhen 518118, China.
Addressing the critical challenges of interfacial defects and insufficient stability in perovskite solar cells, this work introduces a co-solvent engineering strategy to dynamically regulate the phenethylammonium chloride (PEACl) passivation layer. The effect of isopropyl alcohol (IPA) and a DMSO: IPA (1:100) mixture as solvent for forming the PEACl 2D passivation layer is systematically explored, and the synergistic interplay between solvent coordination strength and crystallization kinetics is systematically investigated. The DMSO: IPA (1:100) blend balances Pb-O coordination (via DMSO) and rapid phase separation (via IPA), enabling the oriented growth of a dense, ultrathin 2D perovskite overlayer.
View Article and Find Full Text PDFAdv Mater
June 2024
Institute for Photovoltaics, University of Stuttgart, Pfaffenwaldring 47, 70569, Stuttgart, Germany.
This work introduces a simplified deposition procedure for multidimensional (2D/3D) perovskite thin films, integrating a phenethylammonium chloride (PEACl)-treatment into the antisolvent step when forming the 3D perovskite. This simultaneous deposition and passivation strategy reduces the number of synthesis steps while simultaneously stabilizing the halide perovskite film and improving the photovoltaic performance of resulting solar cell devices to 20.8%.
View Article and Find Full Text PDFNanoscale
June 2020
State Key Laboratory of Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, 2699 Qianjin Street, Changchun 130012, China.
All inorganic perovskite quantum dots (QDs) (CsPbX3, X = Cl, Br, I) have been applied on light-emitting devices (LEDs) in recent years due to their excellent optical and optoelectronic properties. However, blue-light emitting perovskite QD LEDs (PQD-LEDs) exhibit poor performances compared with their green- and red-light emitting counterparts. Herein, we fabricated high performing blue-light emitting PQD-LEDs based on phenethylammonium chloride (PEACl) modified CsPb(Cl/Br)3 QDs.
View Article and Find Full Text PDF