TY - JOUR
T1 - Conjugated Organic Cations Enable Efficient Self-Healing FASnI3 Solar Cells
AU - Ran, Chenxin
AU - Gao, Weiyin
AU - Li, Jingrui
AU - Xi, Jun
AU - Li, Lu
AU - Dai, Jinfei
AU - Yang, Yingguo
AU - Gao, Xingyu
AU - Dong, Hua
AU - Jiao, Bo
AU - Spanopoulos, Ioannis
AU - Malliakas, Christos D.
AU - Hou, Xun
AU - Kanatzidis, Mercouri G.
AU - Wu, Zhaoxin
N1 - Funding Information:
This work was financially supported by the National Natural Science Foundation of China (grant nos. 61935016, 11574248, 51802253), the Fundamental Research Funds for the Central Universities (grant nos. xjj2018018 and xjj2016031), and China Postdoctoral Science Foundation (grant nos. 2017M613137 and 2018M643649). The SEM work was done at the International Center for Dielectric Research (ICDR), Xi'an Jiaotong University, Xi'an, China. The work at Northwestern University was supported in part by the LEAP Center, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, and Office of Basic Energy Sciences under award DE-SC0001059 (sample fabrication and characterization). Z.W. and C.R. conceived the idea and designed the experiment. L.L. J.X. and J.D. synthesized the PPA and characterized the samples and analyzed the data. C.R. and W.G. fabricated, characterized, and optimized perovskite thin film and PSC devices. J.L. carried out and analyzed the theoretical calculation. W.G. J.X. H.D. B.J. I.S. and C.D.M. provided constructive discussion on the experimental data. Y.Y. and X.G. carried out the 2D-GIXRD and analyzed the data. Z.W. supervised this project. C.R. M.G.K. and Z.W. wrote the manuscript and all authors contributed to the editing of the manuscript. The authors declare no competing interests.
Funding Information:
This work was financially supported by the National Natural Science Foundation of China (grant nos. 61935016 , 11574248 , 51802253 ), the Fundamental Research Funds for the Central Universities (grant nos. xjj2018018 and xjj2016031 ), and China Postdoctoral Science Foundation (grant nos. 2017M613137 and 2018M643649 ). The SEM work was done at the International Center for Dielectric Research (ICDR), Xi’an Jiaotong University , Xi’an, China. The work at Northwestern University was supported in part by the LEAP Center, an Energy Frontier Research Center funded by the U.S. Department of Energy , Office of Science , and Office of Basic Energy Sciences under award DE-SC0001059 (sample fabrication and characterization).
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/12/18
Y1 - 2019/12/18
N2 - The introduction of large-volume amines (LVAs) in Sn-based perovskite films has been shown to lead to promising power conversion efficiency (PCE) in Pb-free perovskite solar cells (PSCs). However, the LVAs adopted so far (e.g., phenylethylammonium [PEA] and butylammonium [BA]) are insulating and could impede charge extraction within the perovskite film. Herein, a conjugated LVA, 3-phenyl-2-propen-1-amine (PPA), is introduced in formamidinium tin iodide (FASnI3) perovskite. Our results show that the incorporation of PPA results in enlarged grain sizes, reduced trap density, preferential orientation, efficient charge extraction, and enhanced structural stability of FASnI3 film. These positive effects help in achieving efficient PSCs with a PCE as high as 9.61% with negligible hysteresis and outstanding stability (remains 92% of its initial PCE value after 1,440 h). Furthermore, the presence of PPA enables a self-healing action of PSCs. Most importantly, we report large-area (1 × 1 cm2) Sn-based PSCs achieving PCE of 7.08%. For ecofriendly concerns, Sn-based PSCs have been extensively studied and made inspiring progress during the past few years. Recently, the introduction of large-volume amines (LVAs) (e.g., phenylethylammonium [PEA] and butylammonium [BA]) have shown their promise in enhancing the performance of FASnI3-based PSCs. However, the insulating nature of these LVAs sets limitations on the charge extraction of the film. Herein, a conjugated LVA, 3-phenyl-2-propen-1-amine (PPA), is introduced aiming at promoting charge extraction within FASnI3 film. The presence of PPA is found to enlarge the grain size, passivate the grains, and induce the orientation of the film. These merits of PPA deliver PSCs with PCE of 9.61% on 0.09 cm2 and 7.08% on 1 cm2. Moreover, PPA-based PSCs exhibit robust stability and self-healing behavior. This work sheds critical lights on improving the quality of perovskite film by molecular design of organic cations and highlights the promise of Pb-free PSCs. A conjugated large-volume cation is adopted as an additive to modify FASnI3 film with much improved film quality. Lead-free PSC devices with PCE of 9.61% on 0.09 cm2 and 7.08% on 1 cm2 can be achieved. The PSC devices also show robust stability with self-healing ability. This work addresses the promise of Sn-based PSCs and takes a big step forward in the field of ecofriendly lead-free photovoltaic devices.
AB - The introduction of large-volume amines (LVAs) in Sn-based perovskite films has been shown to lead to promising power conversion efficiency (PCE) in Pb-free perovskite solar cells (PSCs). However, the LVAs adopted so far (e.g., phenylethylammonium [PEA] and butylammonium [BA]) are insulating and could impede charge extraction within the perovskite film. Herein, a conjugated LVA, 3-phenyl-2-propen-1-amine (PPA), is introduced in formamidinium tin iodide (FASnI3) perovskite. Our results show that the incorporation of PPA results in enlarged grain sizes, reduced trap density, preferential orientation, efficient charge extraction, and enhanced structural stability of FASnI3 film. These positive effects help in achieving efficient PSCs with a PCE as high as 9.61% with negligible hysteresis and outstanding stability (remains 92% of its initial PCE value after 1,440 h). Furthermore, the presence of PPA enables a self-healing action of PSCs. Most importantly, we report large-area (1 × 1 cm2) Sn-based PSCs achieving PCE of 7.08%. For ecofriendly concerns, Sn-based PSCs have been extensively studied and made inspiring progress during the past few years. Recently, the introduction of large-volume amines (LVAs) (e.g., phenylethylammonium [PEA] and butylammonium [BA]) have shown their promise in enhancing the performance of FASnI3-based PSCs. However, the insulating nature of these LVAs sets limitations on the charge extraction of the film. Herein, a conjugated LVA, 3-phenyl-2-propen-1-amine (PPA), is introduced aiming at promoting charge extraction within FASnI3 film. The presence of PPA is found to enlarge the grain size, passivate the grains, and induce the orientation of the film. These merits of PPA deliver PSCs with PCE of 9.61% on 0.09 cm2 and 7.08% on 1 cm2. Moreover, PPA-based PSCs exhibit robust stability and self-healing behavior. This work sheds critical lights on improving the quality of perovskite film by molecular design of organic cations and highlights the promise of Pb-free PSCs. A conjugated large-volume cation is adopted as an additive to modify FASnI3 film with much improved film quality. Lead-free PSC devices with PCE of 9.61% on 0.09 cm2 and 7.08% on 1 cm2 can be achieved. The PSC devices also show robust stability with self-healing ability. This work addresses the promise of Sn-based PSCs and takes a big step forward in the field of ecofriendly lead-free photovoltaic devices.
KW - conjugated cation
KW - formamidinium tin iodide
KW - large-area device
KW - lead-free perovskite
KW - orientation
KW - preferential
KW - self-healing
KW - solar cells
KW - stability
UR - http://www.scopus.com/inward/record.url?scp=85076213475&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076213475&partnerID=8YFLogxK
U2 - 10.1016/j.joule.2019.08.023
DO - 10.1016/j.joule.2019.08.023
M3 - Article
AN - SCOPUS:85076213475
SN - 2542-4351
VL - 3
SP - 3072
EP - 3087
JO - Joule
JF - Joule
IS - 12
ER -