Open AccessOrganic Ligands Armored ZnO Enhances Efficiency and Stability of CsPbI 2 Br Perovskite Solar Cells
Author(s) -
Wang Pang,
Wang Hui,
Mao Yuchao,
Zhang Huijun,
Ye Fanghao,
Liu Dan,
Wang Tao
Publication year - 2020
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.202000421
Subject(s) - passivation , materials science , perovskite (structure) , crystallinity , thermal stability , doping , chemical engineering , fabrication , degradation (telecommunications) , energy conversion efficiency , nanotechnology , layer (electronics) , optoelectronics , composite material , medicine , telecommunications , alternative medicine , pathology , computer science , engineering
Inorganic perovskite solar cells (PSCs) have witnessed great progress in recent years due to their superior thermal stability. As a representative, CsPbI 2 Br is attracting considerable attention as it can balance the high efficiency of CsPbI 3 and the stability of CsPbBr 3 . However, most research employs doped charge transport materials or applies bilayer transport layers to obtain decent performance, which vastly complicates the fabrication process and scarcely satisfies the commercial production requirement. In this work, all‐layer‐doping‐free inorganic CsPbI 2 Br PSCs using organic ligands armored ZnO as the electron transport materials achieve an encouraging performance of 16.84%, which is one of the highest efficiencies among published works. Meanwhile, both the ZnO‐based CsPbI 2 Br film and device show superior photostability under continuous white light‐emitting diode illumination and improved thermal stability under 85 °C. The remarkable enhanced performance arises from the favorable organic ligands (acetate ions) residue in the ZnO film, which not only can conduce to maintain high crystallinity of perovskite, but also passivate traps at the interface through cesium/acetate interactions, thus suppressing the photo‐ and thermal‐ induced perovskite degradation.