Premium
Efficient Mixed‐Cation Mixed‐Halide Perovskite Solar Cells by All‐Vacuum Sequential Deposition Using Metal Oxide Electron Transport Layer
Author(s) -
Kam Matthew,
Zhu Yiyi,
Zhang Daquan,
Gu Leilei,
Chen Jiaqi,
Fan Zhiyong
Publication year - 2019
Publication title -
solar rrl
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.544
H-Index - 37
ISSN - 2367-198X
DOI - 10.1002/solr.201900050
Subject(s) - perovskite (structure) , materials science , layer (electronics) , halide , energy conversion efficiency , vacuum deposition , deposition (geology) , optoelectronics , quartz crystal microbalance , thin film , chemical engineering , nanotechnology , inorganic chemistry , chemistry , paleontology , organic chemistry , adsorption , sediment , engineering , biology
The incorporation of various cations and halides to form mixed perovskites has enabled perovskite solar cells (PSCs) to exceed 20% power conversion efficiencies (PCEs). However, they are primarily prepared by solution methods, which limit film uniformity and scalability. Although co‐evaporation is used to prepare all‐vacuum‐deposited PSCs with a decent performance, it involves multiple sources and quartz crystal monitors (QCMs) to simultaneously control deposition rates and film thicknesses, which increase production cost and fabrication complexity and interfere QCMs’ reading precision. Herein, a simple and cost‐effective sequential vapor deposition involving only one QCM and two sources is demonstrated as an advantageous and reliable method to fabricate high‐quality and uniform mixed‐cation mixed‐halide perovskite films with microscale grain sizes and extraordinary morphology for the PSC application. In addition, for the first time, radio frequency (RF)‐sputtered SnO 2 is implemented into all‐vacuum‐deposited PSCs as an electron transport layer (ETL). Together with evaporated copper phthalocyanine (CuPc) as a thermally and chemically stable low‐cost hole transport layer (HTL), alternative to the commonly used 2,2′,7,7′‐tetrakis( N , N ‐di‐ p ‐methoxyphenylamino)‐9,9′‐spirobifluorene (Spiro‐OMeTAD), which is costly, highly hygroscopic, and deliquescent, a respectable PCE of 15.14% is achieved with a promising device stability and negligible hysteresis.