TY - JOUR
T1 - CsI Pre-Intercalation in the Inorganic Framework for Efficient and Stable FA1− x CsxPbI3(Cl) Perovskite Solar Cells
AU - Zhou, Ning
AU - Shen, Yiheng
AU - Zhang, Yu
AU - Xu, Ziqi
AU - Zheng, Guanhaojie
AU - Li, Liang
AU - Chen, Qi
AU - Zhou, Huanping
N1 - Publisher Copyright:
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/6/20
Y1 - 2017/6/20
N2 - Engineering the chemical composition of organic and inorganic hybrid perovskite materials is one of the most feasible methods to boost the efficiency of perovskite solar cells with improved device stability. Among the diverse hybrid perovskite family of ABX3, formamidinium (FA)-based mixed perovskite (e.g., FA1− xCsxPbI3) possesses optimum bandgaps, superior optoelectronic property, as well as thermal- and photostability, which is proven to be the most promising candidate for advanced solar cell. Here, FA0.9Cs0.1PbI3(Cl) is implemented as the light-harvesting layer in planar devices, whereas a low temperature, two-step solution deposition method is employed for the first time in this materials system. This paper comprehensively exploits the role of Cs+ in the FA0.9Cs0.1PbI3(Cl) perovskite that affects the precursor chemistry, film nucleation and grain growth, and defect property via pre-intercalation of CsI in the inorganic framework. In addition, the resultant FA0.9Cs0.1PbI3(Cl) films are demonstrated to exhibit an improved optoelectronic property with an elevated device power conversion efficiency (PCE) of 18.6%, as well as a stable phase with substantial enhancement in humidity and thermal stability, as compared to that of FAPbI3(Cl). The present method is able to be further extended to a more complicated (FA,MA,Cs)PbX3 material system by delivering a PCE of 19.8%.
AB - Engineering the chemical composition of organic and inorganic hybrid perovskite materials is one of the most feasible methods to boost the efficiency of perovskite solar cells with improved device stability. Among the diverse hybrid perovskite family of ABX3, formamidinium (FA)-based mixed perovskite (e.g., FA1− xCsxPbI3) possesses optimum bandgaps, superior optoelectronic property, as well as thermal- and photostability, which is proven to be the most promising candidate for advanced solar cell. Here, FA0.9Cs0.1PbI3(Cl) is implemented as the light-harvesting layer in planar devices, whereas a low temperature, two-step solution deposition method is employed for the first time in this materials system. This paper comprehensively exploits the role of Cs+ in the FA0.9Cs0.1PbI3(Cl) perovskite that affects the precursor chemistry, film nucleation and grain growth, and defect property via pre-intercalation of CsI in the inorganic framework. In addition, the resultant FA0.9Cs0.1PbI3(Cl) films are demonstrated to exhibit an improved optoelectronic property with an elevated device power conversion efficiency (PCE) of 18.6%, as well as a stable phase with substantial enhancement in humidity and thermal stability, as compared to that of FAPbI3(Cl). The present method is able to be further extended to a more complicated (FA,MA,Cs)PbX3 material system by delivering a PCE of 19.8%.
KW - cesium
KW - defect density
KW - formamidinium
KW - perovskite solar cells
KW - precursor chemistry
UR - http://www.scopus.com/inward/record.url?scp=85019006343&partnerID=8YFLogxK
U2 - 10.1002/smll.201700484
DO - 10.1002/smll.201700484
M3 - Article
C2 - 28464500
AN - SCOPUS:85019006343
SN - 1613-6810
VL - 13
JO - Small
JF - Small
IS - 23
M1 - 1700484
ER -