The CsPbI inorganic perovskite is a potential candidate for fabricating long-term operational photovoltaic devices owing to its intrinsic superb thermal stability. However, the carbon-based CsPbI perovskite solar cells (C-PSCs) without hole transport material (HTM) are currently disadvantaged by their relatively low power conversion efficiency resulting from the poor grain quality and mismatched energy band levels of the as-made CsPbI films. Herein we demonstrate that by doping Na into the CsPbI lattice, the grain quality is significantly improved with low defect density, and also, the energy band levels are better matched to the contact electrodes, affording a higher built-in potential. Consequently, the V of the C-PSCs is drastically increased from 0.77 to 0.92 V, and the efficiency from 8.6% to 10.7%, a record value for the CsPbI PSCs without HTM. Moreover, the non-encapsulated device showed virtually no performance degradation after 70 days of storage in air atmosphere.
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http://dx.doi.org/10.1016/j.isci.2019.04.025 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, No. 483 Wushan Road, Guangzhou 510642, China.
Interface engineering strategies passivate defects on the polycrystalline perovskite film surface and improve the stability of corresponding perovskite solar cells (PSCs). However, a single interface engineering step can result in restricted benefits on various occasions. Therefore, an appropriate additional modification step can be necessary to synergistically improve the device performance.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
College of Chemical and Biological Engineering, Shandong University of Science and Technology, Qingdao, 266590, PR China.
Air-processed perovskite solar cells are desirable for the large-scale manufacturing application in the future, yet the presence of moisture and oxygen goes against perovskite crystallization and deteriorates phase stabilization, leading to the formation of substantial defective nano-impurities, especially on the vulnerable surface. Here, we propose a strategy to simultaneously remove superficial defect layer and solidify the surface by soaking air-fabricated perovskite film into low-polar organic esters at elevated temperature to trigger an in situ dynamic surface lattice disassemble and reconstruction process. Molecular dynamics simulations and experimental results indicate that the inorganic CsPbIBr perovskite is first dissolved and then the Br-rich phase is recrystallized at solid-liquid interface owing to the balance between weak solubility and high-temperature induced annealing process, thus hardening the soft surface and releasing the lattice tensile stress, which benefits the minimization of interfacial recombination and improvement of the structural stability.
View Article and Find Full Text PDFSmall
November 2024
Institute of Functional Nano & Soft Materials (FUNSOM), Joint International Research Laboratory of Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu, 215123, P. R. China.
Wide-bandgap perovskite sub-cells (WPSCs), one of the most crucial components of perovskite-based tandem solar cells (PTSCs), play a critical role in determining the performance of tandem devices. However, confined by the compromised crystallization properties of wide-bandgap perovskites, WPSCs exhibit significantly lower efficiency than their theoretical limit. In particular, for n-i-p structured all-inorganic WPSCs (AIWPSCs), severe nonradiative recombination due to the buried interface defects severely decreases the photovoltaic performance.
View Article and Find Full Text PDFNanomaterials (Basel)
October 2024
School of Science, China University of Geosciences Beijing, Beijing 100083, China.
CsPbIBr, with its suitable bandgap, shows great potential as the top cell in tandem solar cells. Nonetheless, its further development is hindered by a high defect density, severe carrier recombination, and poor stability. In this study, CsPbIBr quantum dots were utilized as an additive in the ethyl acetate anti-solvent, while a layer of CsPbBr QDs was introduced between the ETL and the CsPbIBr light-harvester film.
View Article and Find Full Text PDFSmall
December 2024
LONGi Institute of Future Technology, and School of Materials & Energy, Lanzhou University, 222 South Tianshui Road, Lanzhou, 730000, China.
During fabrication and operation of perovskite solar cells (PSCs), defects commonly arise within the crystals as well as at grain boundaries. However, conventional additive strategies typically only serve to mitigate the occurrence of a single defect and fail to significantly enhance device performance. Herein, carbon-based hole-transport-layer-free CsPbIBr devices are focused on, one kind of important PSCs with more stable structure and an appropriate bandgap for a semitransparent solar cell or a top cell in a tandem configuration, and present a highly efficient one-stone-for-multiple-birds additive strategy based on lanthanide trifluoromethanesulfonates (Ln(OTF), Ln: neodymium (Nd), europium (Eu), dysprosium (Dy), thulium (Tm)).
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