材料科学
光伏
钙钛矿(结构)
制作
光伏系统
化学工程
纳米技术
水溶液
能量转换效率
非阻塞I/O
光电子学
电气工程
工程类
病理
物理化学
医学
催化作用
化学
生物化学
替代医学
作者
William J. Scheideler,Nicholas Rolston,Oliver Zhao,Jinbao Zhang,Reinhold H. Dauskardt
标识
DOI:10.1002/aenm.201803600
摘要
Abstract Organometal halide perovskites have powerful intrinsic potential to drive next‐generation solar technology, but their insufficient thermomechanical reliability and unproven large‐area manufacturability limit competition with incumbent silicon photovoltaics. This work addresses these limitations by leveraging large‐area processing and robust inorganic hole transport layers (HTLs). Inverted perovskite solar cells utilizing NiO x HTLs deposited by rapid aqueous spray‐coating that outperform spin‐coated NiO x and lead to a 5× improvement in the fracture energy ( G c ), a primary metric of thermomechanical stability, are presented. The morphology, chemical composition, and optoelectronic properties of the NiO x films are characterized to understand and optimize compatibility with an archetypal double cation perovskite, Cs .17 FA .83 Pb(Br .17 I .83 ) 3 . Perovskite solar cells with sprayed NiO x show higher photovoltaic performance, exhibiting up to 82% fill factor and 17.7% power conversion efficiency (PCE)—the highest PCE reported for inverted cell with scalable charge transport layers—as well as excellent stability under full illumination and after 4000 h aging in inert conditions at room temperature. By utilizing open‐air techniques and aqueous precursors, this combination of robust materials and low‐cost processing provides a platform for scaling perovskite modules with long‐term reliability.
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