TY - JOUR
T1 - Improved Performances of CsPbBr3 Perovskite Solar Cells via PbI2 Additive
AU - Tang, Shu
AU - Hao, Huiying
AU - Yang, Boyuan
AU - Shi, Wanfei
AU - Hamukwaya, Shindume Lomboleni
AU - Dong, Jingjing
AU - Xing, Jie
AU - Liu, Hao
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2025/1/13
Y1 - 2025/1/13
N2 - The emergence of CsPbBr3 perovskite solar cells (PSCs) with a band gap of approximately 2.3 eV has generated increasing interest stemming from their potential for high open-circuit voltage (Voc), making them particularly suitable for use in tandem configurations or spectral splitting. However, the Voc of PSCs currently falls short of its theoretical limit, driven by trap-mediated charge recombination and energy band alignment mismatch. In this study, we present a straightforward additive engineering approach involving the introduction of PbI2 species into the PbBr2 precursor film to form the I-Pb-Br interaction, retarding the rapid reaction between PbBr2 and CsBr. This approach effectively suppresses the Pb-rich phase CsPb2Br5, eliminates pinholes on the CsPbBr3 crystal, and obtains high-quality perovskite films, which can significantly enhance the photovoltaic properties. Consequently, we achieved CsPbBr3 films characterized by enlarged crystal size, complete coverage, high purity, and without pinhole presence, leading to a best-performed efficiency of 10.35% and a higher Voc of up to 1.580 V compared to the power conversion efficiency (PCE) of 8.35% and a Voc of 1.442 V of the control device, along with exceptional operational stability.
AB - The emergence of CsPbBr3 perovskite solar cells (PSCs) with a band gap of approximately 2.3 eV has generated increasing interest stemming from their potential for high open-circuit voltage (Voc), making them particularly suitable for use in tandem configurations or spectral splitting. However, the Voc of PSCs currently falls short of its theoretical limit, driven by trap-mediated charge recombination and energy band alignment mismatch. In this study, we present a straightforward additive engineering approach involving the introduction of PbI2 species into the PbBr2 precursor film to form the I-Pb-Br interaction, retarding the rapid reaction between PbBr2 and CsBr. This approach effectively suppresses the Pb-rich phase CsPb2Br5, eliminates pinholes on the CsPbBr3 crystal, and obtains high-quality perovskite films, which can significantly enhance the photovoltaic properties. Consequently, we achieved CsPbBr3 films characterized by enlarged crystal size, complete coverage, high purity, and without pinhole presence, leading to a best-performed efficiency of 10.35% and a higher Voc of up to 1.580 V compared to the power conversion efficiency (PCE) of 8.35% and a Voc of 1.442 V of the control device, along with exceptional operational stability.
KW - additive engineering
KW - all-inorganic perovskite solar cells
KW - CsPbBr
KW - high-quality film
KW - long-term stability
UR - http://www.scopus.com/inward/record.url?scp=85214990723&partnerID=8YFLogxK
U2 - 10.1021/acsaem.4c02526
DO - 10.1021/acsaem.4c02526
M3 - Article
AN - SCOPUS:85214990723
SN - 2574-0962
VL - 8
SP - 421
EP - 429
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 1
ER -