TY - JOUR
T1 - Combination of Hybrid CVD and Cation Exchange for Upscaling Cs-Substituted Mixed Cation Perovskite Solar Cells with High Efficiency and Stability
AU - Jiang, Yan
AU - Leyden, Matthew R.
AU - Qiu, Longbin
AU - Wang, Shenghao
AU - Ono, Luis K.
AU - Wu, Zhifang
AU - Juarez-Perez, Emilio J.
AU - Qi, Yabing
N1 - Publisher Copyright:
© 2017 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/1/4
Y1 - 2018/1/4
N2 - Mixed cation hybrid perovskites such as CsxFA1− xPbI3 are promising materials for solar cell applications, due to their excellent photoelectronic properties and improved stability. Although power conversion efficiencies (PCEs) as high as 18.16% have been reported, devices are mostly processed by the anti-solvent method, which is difficult for further scaling-up. Here, a method to fabricate CsxFA1− xPbI3 by performing Cs cation exchange on hybrid chemical vapor deposition grown FAPbI3 with the Cs+ ratio adjustable from 0 to 24% is reported. The champion perovskite module based on Cs0.07FA0.93PbI3 with an active area of 12.0 cm2 shows a module PCE of 14.6% and PCE loss/area of 0.17% cm−2, demonstrating the significant advantage of this method toward scaling-up. This in-depth study shows that when the perovskite films prepared by this method contain 6.6% Cs+ in bulk and 15.0% at the surface, that is, Cs0.07FA0.93PbI3, solar cell devices show not only significantly increased PCEs but also substantially improved stability, due to favorable energy level alignment with TiO2 electron transport layer and spiro-MeOTAD hole transport layer, increased grain size, and improved perovskite phase stability.
AB - Mixed cation hybrid perovskites such as CsxFA1− xPbI3 are promising materials for solar cell applications, due to their excellent photoelectronic properties and improved stability. Although power conversion efficiencies (PCEs) as high as 18.16% have been reported, devices are mostly processed by the anti-solvent method, which is difficult for further scaling-up. Here, a method to fabricate CsxFA1− xPbI3 by performing Cs cation exchange on hybrid chemical vapor deposition grown FAPbI3 with the Cs+ ratio adjustable from 0 to 24% is reported. The champion perovskite module based on Cs0.07FA0.93PbI3 with an active area of 12.0 cm2 shows a module PCE of 14.6% and PCE loss/area of 0.17% cm−2, demonstrating the significant advantage of this method toward scaling-up. This in-depth study shows that when the perovskite films prepared by this method contain 6.6% Cs+ in bulk and 15.0% at the surface, that is, Cs0.07FA0.93PbI3, solar cell devices show not only significantly increased PCEs but also substantially improved stability, due to favorable energy level alignment with TiO2 electron transport layer and spiro-MeOTAD hole transport layer, increased grain size, and improved perovskite phase stability.
KW - large area
KW - mixed cation
KW - modules
KW - perovskite solar cell
KW - stability
UR - https://www.scopus.com/pages/publications/85034758762
U2 - 10.1002/adfm.201703835
DO - 10.1002/adfm.201703835
M3 - Article
AN - SCOPUS:85034758762
SN - 1616-301X
VL - 28
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 1
M1 - 1703835
ER -