Cesium-lead based inorganic perovskite quantum-dots as interfacial layer for highly stable perovskite solar cells with exceeding 21% efficiency

dc.contributor.author Akin, Seckin
dc.contributor.author Altintas, Yemliha
dc.contributor.author Mutlugun, Evren
dc.contributor.author Sonmezoglu, Savas
dc.contributor.department AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü en_US
dc.date.accessioned 2021-03-24T12:00:43Z
dc.date.available 2021-03-24T12:00:43Z
dc.date.issued 2019 en_US
dc.description EM acknowledges TUBA GEBIP award. EM and YA acknowledge Abdullah Gul University Scientific Research Project no: FAB-2015-10. en_US
dc.description.abstract Despite the excellent photovoltaic performances of perovskite solar cells (PSCs), the instability of PSCs under severe environment (e.g. humidity, light-induced, etc.) limits further commercialization of such devices. Therefore, in recent years, research on the long-term stability improvement of PSCs has been actively carried out in perovskite field. To address these issues, we demonstrated the incorporation of ultra-thin interfacial layer of inorganic CsPbBr1.85I1.15 perovskite quantum-dots (PQDs) that can effectively passivate defects at or near to the perovskite/hole transport material (HTM) interface, significantly suppressing interfacial recombination. This passivation layer increased the open circuit voltage (V-oc) of triple-cation perovskite cells by as much as 50 mV, with champion cells achieving V-oc similar to 1.14 V. As a result, we obtained hysteresis-free cells with the efficiency beyond 21%. More importantly, devices based on such architecture are capable of resisting humidity and light-induced. Remarkably, the device employing CsPbBr1.85I1.15 demonstrated a superb shelf-stability aganist to humidity under ambient conditions (R.H. >= 40%), retaining nearly 91% of initial efficiency after 30 days, while the efficiency of control device rapidly dropped to 45% from its initial value under the same conditions. Besides benefiting from the high moisture resistivity as well as supressed ion migration, PSC5 based on PQDs showed better operational stability (retaining 94% of their initial performance) than that of the PQDs-free one under continuous light irradiation over 400 h. In addition, a faster PL decay time of 4.66 ns was attained for perovskite/PQDs structure (5.77 ns for only PQDs structure) due to the favorable energy transfer at the interface, indicating a Forster resonance energy transfer (FRET) mechanism. This work indicates that inorganic PQDs are important materials as interlayer in PSC5 to supremely enhance the device stability and efficiency. en_US
dc.description.sponsorship Turkish Academy of Sciences Abdullah Gul University FAB-2015-10 en_US
dc.identifier.endpage 566 en_US
dc.identifier.issn 2211-2855
dc.identifier.issn 2211-3282
dc.identifier.startpage 557 en_US
dc.identifier.uri https://doi.org/10.1016/j.nanoen.2019.03.091
dc.identifier.uri https://hdl.handle.net/20.500.12573/619
dc.identifier.volume Volume: 60 en_US
dc.language.iso eng en_US
dc.publisher ELSEVIER, RADARWEG 29, 1043 NX AMSTERDAM, NETHERLANDS en_US
dc.relation.isversionof 10.1016/j.nanoen.2019.03.091 en_US
dc.relation.journal NANO ENERGY en_US
dc.relation.publicationcategory Makale - Uluslararası - Editör Denetimli Dergi en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Perovskite solar cells en_US
dc.subject Stability en_US
dc.subject Interfacial layer en_US
dc.subject CsPbBrxI3-x inorganic perovskite quantum-dots en_US
dc.title Cesium-lead based inorganic perovskite quantum-dots as interfacial layer for highly stable perovskite solar cells with exceeding 21% efficiency en_US
dc.type article en_US

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