Los puntos clave no están disponibles para este artículo en este momento.
Abstract High‐quality charge carrier transport materials are of key importance for stable and efficient perovskite‐based photovoltaics. This work reports on electron‐beam‐evaporated nickel oxide (NiO x ) layers, resulting in stable power conversion efficiencies (PCEs) of up to 18.5% when integrated into solar cells employing inkjet‐printed perovskite absorbers. By adding oxygen as a process gas and optimizing the layer thickness, transparent and efficient NiO x hole transport layers (HTLs) are fabricated, exhibiting an average absorptance of only 1%. The versatility of the material is demonstrated for different absorber compositions and deposition techniques. As another highlight of this work, all‐evaporated perovskite solar cells employing an inorganic NiO x HTL are presented, achieving stable PCEs of up to 15.4%. Along with good PCEs, devices with electron‐beam‐evaporated NiO x show improved stability under realistic operating conditions with negligible degradation after 40 h of maximum power point tracking at 75 °C. Additionally, a strong improvement in device stability under ultraviolet radiation is found if compared to conventional perovskite solar cell architectures employing other metal oxide charge transport layers (e.g., titanium dioxide). Finally, an all‐evaporated perovskite solar mini‐module with a NiO x HTL is presented, reaching a PCE of 12.4% on an active device area of 2.3 cm 2 .
Building similarity graph...
Analyzing shared references across papers
Loading...
Tobias Abzieher
National Renewable Energy Laboratory
Somayeh Moghadamzadeh
Karlsruhe Institute of Technology
Fabian Schackmar
Karlsruhe Institute of Technology
Advanced Energy Materials
Karlsruhe Institute of Technology
Helmholtz-Zentrum Berlin für Materialien und Energie
Building similarity graph...
Analyzing shared references across papers
Loading...
Abzieher et al. (Mon,) studied this question.
synapsesocial.com/papers/6a1b46ff0ea968f653abaef6 — DOI: https://doi.org/10.1002/aenm.201802995