Reconfigurable photovoltaic modules are a promising approach to improve the energy yield of partially shaded systems. So far, the feasibility of this concept has been evaluated through simulations or simplified experiments. In this work, we analyse the outdoor performance of a full-scale prototype of a series-parallel photovoltaic module with six reconfigurable blocks. Over a 4-month-long period, its performance was compared to a reference photovoltaic module with static interconnections and six bypass diodes. The results show that under partial shading, the reconfigurable module produced 10.2% more energy than the reference module. In contrast, under uniform illumination the energy yield of the reconfigurable PV module was 1.9% lower due to the additional losses introduced by its switching matrix. Finally, a modification in the reconfiguration algorithm is proposed to reduce the output current-voltage range of the module and simplify the design of module-level power converters while limiting the shading tolerance loss.
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http://dx.doi.org/10.1038/s41467-023-43927-3 | DOI Listing |
Data Brief
December 2024
Department of Computer Systems Engineering, Faculty of Information and Communication Technology, Tshwane University of Technology, South Africa.
Solar energy has become the fastest growing renewable and alternative source of energy. However, there is little or no open-source datasets to advance research knowledge in photovoltaic related systems. The work presented in this article is a step towards deriving Photo-Voltaic Module Dataset (PVMD) of thermal images and ensuring they are publicly available.
View Article and Find Full Text PDFHeliyon
December 2024
Mechanical Engineering Division, Faculty of Engineering, Khon Kaen University, Thailand.
Phase change materials (PCMs) have been widely recognized as a highly efficient medium for thermal energy storage. Many studies have identified the low thermal conductivity of PCMs. In the current investigation, the researchers have blended PCM with nanoparticles to enhance its thermal conductivity and electrical efficiency.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Applied Chemistry and Institute of Molecular Science, National Yang Ming Chiao Tung University, 1001 Ta-Hseuh Road, Hsinchu 300093, Taiwan.
Three new bithiophene imide (BTI)-based organic small molecules, (), (), and (), with varied alkyl side chains, were developed and employed as self-assembled monolayers (SAMs) applied to NiOx films in tin perovskite solar cells (TPSCs). The NiOx layer has the effect of modifying the hydrophilicity and the surface roughness of ITO for SAM to uniformly deposit on it. The side chains of the SAM molecules play a vital role in the formation of a high-quality perovskite layer in TPSCs.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Flexible Sensing Technology, Institute of Chemical Engineering, Guangdong Academy of Sciences, Guangzhou 510665, China.
The global solar market is booming with a rapid growth in installed integrated devices, while photovoltaic (PV) systems are suffering from waste heat, which causes the decline of the photovoltaic conversion efficiency (PCE). This study presents the seamless integration of the ionic thermoelectric generator (iTEG) layer with traditional PV modules, facilitating the exploitation of waste heat and augmenting the overall power output. Experimental results validate the effectiveness of the iTEG, demonstrating substantial power generation and a consistent energy output.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Nankai University, Colege of Chemistry, CHINA.
Organic photovoltaic materials that can be processed via non-halogenated solvents are crucial for the large-area manufacturing of organic solar cells (OSCs). However, the limited available of electron acceptors with adequate solubility and favorable molecular packing presents a challenge in achieving efficient non-halogenated solvent-processed OSCs. Herein, inspired by the three-dimensional dimeric acceptor CH8-4, we employed a molecular isomerization strategy to synthesize its isomers, CH8-4A and CH8-4B, by tuning the position of fluorine (F) atom in the central unit.
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