TY - JOUR
T1 - Triethylsilane introduced precursor engineering towards efficient and stable perovskite solar cells
AU - Huang, Yuanmei
AU - Zhou, Wencai
AU - Zhong, Huaying
AU - Chen, Wei
AU - Yu, Guoping
AU - Zhang, Wenjie
AU - Wang, Shuanglin
AU - Sui, Yujie
AU - Yang, Xin
AU - Zhuang, Yu
AU - Tang, Jun
AU - Cao, Leifeng
AU - Müller-Buschbaum, Peter
AU - Aierken, Abuduwayiti
AU - Han, Peigang
AU - Tang, Zeguo
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2024/3
Y1 - 2024/3
N2 - Perovskite solar cells (PSCs) are believed to be optimistic for commercial deployment soon since the power conversion efficiency of PSCs presently reaches up to 26.10 % due to the intensive efforts these years. The two-step method is comparatively more suitable for scalable perovskite films, where lead halides and ammonium salts are prepared in separate precursors and deposited sequentially. Therefore, the reactivity between these two precursors governs the quality of final perovskite films and the intrinsic non-radiative recombination (NRR) at the perovskite's interfaces. Herein, we empowered both types of precursors, one by one and then simultaneously, with triethylsilane (TES) to investigate its effect on the (FAPbI3)1-x (MAPbBr3)x perovskite's morphological and optoelectronic properties. TES, with ethyl moieties and metalloid center, in ammonium salts delivers homogeneous perovskites' crystals and inhibits the NRR of perovskite films by reducing the defects and trap states. As a result, the optimized devices exhibit not only improved device performance (particularly for the increased fill factors and open circuit voltages) but also enhanced stabilities.
AB - Perovskite solar cells (PSCs) are believed to be optimistic for commercial deployment soon since the power conversion efficiency of PSCs presently reaches up to 26.10 % due to the intensive efforts these years. The two-step method is comparatively more suitable for scalable perovskite films, where lead halides and ammonium salts are prepared in separate precursors and deposited sequentially. Therefore, the reactivity between these two precursors governs the quality of final perovskite films and the intrinsic non-radiative recombination (NRR) at the perovskite's interfaces. Herein, we empowered both types of precursors, one by one and then simultaneously, with triethylsilane (TES) to investigate its effect on the (FAPbI3)1-x (MAPbBr3)x perovskite's morphological and optoelectronic properties. TES, with ethyl moieties and metalloid center, in ammonium salts delivers homogeneous perovskites' crystals and inhibits the NRR of perovskite films by reducing the defects and trap states. As a result, the optimized devices exhibit not only improved device performance (particularly for the increased fill factors and open circuit voltages) but also enhanced stabilities.
KW - Precursor engineering
KW - Stability
KW - Triethylsilane
KW - Two-step method
UR - http://www.scopus.com/inward/record.url?scp=85178633169&partnerID=8YFLogxK
U2 - 10.1016/j.mtadv.2023.100449
DO - 10.1016/j.mtadv.2023.100449
M3 - Article
AN - SCOPUS:85178633169
SN - 2590-0498
VL - 21
JO - Materials Today Advances
JF - Materials Today Advances
M1 - 100449
ER -