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All-Inorganic Perovskite Solar Cells Based on CsPbIBr(2) and Metal Oxide Transport Layers with Improved Stability

Despite the successful improvement in the power conversion efficiency (PCE) of perovskite solar cells (PSCs), the issue of instability is still a serious challenge for their commercial application. The issue of the PSCs mainly originates from the decomposition of the organic–inorganic hybrid perovsk...

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Detalles Bibliográficos
Autores principales: Yang, Jien, Zhang, Qiong, Xu, Jinjin, Liu, Hairui, Qin, Ruiping, Zhai, Haifa, Chen, Songhua, Yuan, Mingjian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956066/
https://www.ncbi.nlm.nih.gov/pubmed/31766695
http://dx.doi.org/10.3390/nano9121666
Descripción
Sumario:Despite the successful improvement in the power conversion efficiency (PCE) of perovskite solar cells (PSCs), the issue of instability is still a serious challenge for their commercial application. The issue of the PSCs mainly originates from the decomposition of the organic–inorganic hybrid perovskite materials, which will degrade upon humidity and suffer from the thermal environment. In addition, the charge transport layers also influence the stability of the whole devices. In this study, inorganic transport layers are utilized in an inverted structure of PSCs employing CsPbIBr(2) as light absorbent layer, in which nickel oxide (NiO(x)) and cerium oxide (CeO(x)) films are applied as the hole transport layer (HTL) and the electron transport layer (ETL), respectively. The inorganic transport layers are expected to protect the CsPbIBr(2) film from the contact of moisture and react with the metal electrode, thus preventing degradation. The PSC with all inorganic components, inorganic perovskite and inorganic transport layers demonstrates an initial PCE of 5.60% and retains 5.56% after 600 s in ambient air at maximum power point tracking.