2D Ruddlesden-Popper perovskite (RPP) solar cells have excellent environmental stability. However, the power conversion efficiency (PCE) of RPP cells remains inferior to 3D perovskite-based cells. Herein, 2D (CH (CH ) NH ) (CH NH ) Pb I perovskite cells with different numbers of [PbI ] sheets (n = 2-4) are analyzed. Photoluminescence quantum yield (PLQY) measurements show that nonradiative open-circuit voltage (V ) losses outweigh radiative losses in materials with n > 2. The n = 3 and n = 4 films exhibit a higher PLQY than the standard 3D methylammonium lead iodide perovskite although this is accompanied by increased interfacial recombination at the top perovskite/C interface. This tradeoff results in a similar PLQY in all devices, including the n = 2 system where the perovskite bulk dominates the recombination properties of the cell. In most cases the quasi-Fermi level splitting matches the device V within 20 meV, which indicates minimal recombination losses at the metal contacts. The results show that poor charge transport rather than exciton dissociation is the primary reason for the reduction in fill factor of the RPP devices. Optimized n = 4 RPP solar cells had PCEs of 13% with significant potential for further improvements.
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http://dx.doi.org/10.1002/adma.201901090 | DOI Listing |
Light Sci Appl
January 2025
Executive Management College of CHN ENERGY, No.7 Binhe Avenue, North District of Future Science City, Changping District, Beijing, 102211, China.
In 2012, Prof. Henry Snaith demonstrated the first solid-state perovskite solar cell (PSC) with an efficiency of 10.9%, igniting a surge of interest and research into perovskite materials for their potential to revolutionize the photovoltaic (PV) industry.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning 116023, China.
In recent years, perovskite solar cells (PSCs) have garnered considerable attention as a prime candidate for next-generation photovoltaic technology. Ensuring the structural stability of perovskites is crucial to the operational reliability of these devices. However, the nonphotoactive yellow phase (δ-FAPbI) of formamidine (FA)-based perovskites is more favorable in thermodynamics, making it challenging to achieve pure α phase in crystallization.
View Article and Find Full Text PDFAdv Mater
December 2024
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids and State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Highly efficient nonfullerene acceptors (NFAs) for organic solar cells (OSCs) with low energy loss (E) and favorable morphology are critical for breaking the efficiency bottleneck and achieving commercial applications of OSCs. In this work, quinoxaline-based NFAs are designed and synthesized using a synergistic isomerization and bromination approach. The π-expanded quinoxaline-fused core exhibits different bromination sites for isomeric NFAs, namely AQx-21 and AQx-22.
View Article and Find Full Text PDFSmall
December 2024
Dalian National Laboratory for Clean Energy, iChEM, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, P. R. China.
Formamidine lead iodide (FAPbI) quantum dots (QDs) have attracted great attention as a new generation of photovoltaic material due to their long carrier diffusion length, benign ambient stability, and light-harvesting ability. However, its large surface area with inherent thermodynamic instability and highly defective ionic termination are still major obstacles to fabricating high-performance devices. Herein, a metallic ion dopant is developed to post-treat FAPbI QDs immediately after their fabrication by using a metal-glutamate salt solution.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Nantes Université: Nantes Universite, Chemistry, FRANCE.
Chalcogenide-based thin-film solar cell optimized for rear illumination and used for CO2 reduction is presented. Central to this innovation is a thinner, Cu(In,Ga)S2 chalcopyrite absorber coated with a robust metallic top layer, which potentially surpasses the performance of conventional front-illuminated designs. Using cobalt quaterpyridine molecular catalyst, photocurrent densities for CO2 reduction exceeding 10 mA/cm2 at 0.
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