Autor segons l'article: Ramirez-Como, Magaly; Moustafa, Enas; Samir, Mohamed; Torimtubun, Alfonsina Abat Amelenan; Sanchez, Jose G; Pallares, Josep; Marsal, Lluis F
Departament: Enginyeria Electrònica, Elèctrica i Automàtica
Autor/s de la URV: Marsal Garví, Luis Francisco / Pallarès Marzal, Josep / SANCHEZ LÓPEZ, JOSÉ GUADALUPE / Torimtubun, Alfonsina Abat Amelenan
Paraules clau: Zno Transport Stability Origin Mechanisms Impedance spectroscopy High-performance High-efficiency Fabrication Enhancement
Resum: Organic solar cells (OSCs) have reached an efficiency near 20%; however, their low long-term stability is the main limitation to their industrialization. In this work, we investigated the degradation of bulk heterojunction non-fullerene solar cells (NFA-OSCs) based on PM6:Y7 with an efficiency of 17.5%. The degradation analysis was carried out following the established ISOS-D-1 protocol under different degradation conditions: N-2 atmosphere (H2O < 0.1 ppm and O-2 < 0.1 ppm) and encapsulated devices and non-encapsulated devices exposed to ambient conditions (60 & PLUSMN; 5% relative humidity). The evolution of the current density-voltage (J-V) and impedance spectroscopy (IS) measurements were used to analyse the degradation process during 1000 h and its relationship with physical mechanisms. The degradation of encapsulated and non-encapsulated devices is mainly caused by the drop in the open circuit voltage (V-OC). For devices exposed to the N-2 atmosphere, the fill factor (FF) was the most affected parameter. The dependence of short circuit current density (J(SC)) versus light intensity study reveals that the efficiency of non-encapsulated devices decreases faster due to a higher bimolecular recombination degree. The devices under a N-2 atmosphere and those encapsulated showed T-80 lifetimes of 1000 h and 336 h, respectively, whereas the non-encapsulated devices have a short T-80 lifetime of less than 24 h. The analysis of the efficiency decay was used to identify the different degradation mechanisms (by diffused environmental water or oxygen or by intrinsic polymer chemical reactions) under different conditions. The degradation origin of the active layer and interlayers was investigated through impedance spectroscopy measurements.
Àrees temàtiques: Renewable energy, sustainability and the environment Materials science, multidisciplinary Fuel technology Energy engineering and power technology Energy & fuels Chemistry, physical
Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
Adreça de correu electrònic de l'autor: alfonsina.abat@estudiants.urv.cat alfonsina.abat@estudiants.urv.cat josep.pallares@urv.cat lluis.marsal@urv.cat
Identificador de l'autor: 0000-0001-8012-4772 0000-0001-8012-4772 0000-0001-7221-5383 0000-0002-5976-1408
Data d'alta del registre: 2024-10-12
Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
Enllaç font original: https://pubs.rsc.org/en/content/articlelanding/2023/se/d3se00703k
URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
Referència a l'article segons font original: Sustainable Energy & Fuels. 7 (16): 3883-3892
Referència de l'ítem segons les normes APA: Ramirez-Como, Magaly; Moustafa, Enas; Samir, Mohamed; Torimtubun, Alfonsina Abat Amelenan; Sanchez, Jose G; Pallares, Josep; Marsal, Lluis F (2023). Understanding the role of interfacial layers in the photostability of PM6:Y7-based organic solar cells under different degradation conditions. Sustainable Energy & Fuels, 7(16), 3883-3892. DOI: 10.1039/d3se00703k
DOI de l'article: 10.1039/d3se00703k
Entitat: Universitat Rovira i Virgili
Any de publicació de la revista: 2023
Tipus de publicació: Journal Publications