TY - JOUR
T1 - Molecular-Extrusion-Driven Halogen Homogenization for Efficient Perovskite-Silicon Tandem Solar Cells
AU - Chen, Yu
AU - Peng, Yang
AU - Luo, Chuan
AU - Shen, Yang
AU - Lin, Pu An
AU - Zhou, Jing
AU - Wu, Xing
AU - Liu, Songlin
AU - Chen, Hao
AU - Bai, Sai
AU - Wu, Yihui
AU - Peng, Qiang
N1 - Publisher Copyright:
© 2026 Wiley-VCH GmbH.
PY - 2026
Y1 - 2026
N2 - Phase segregation is an inevitable phenomenon in wide-bandgap perovskites, triggering nonradiative recombination and degrading device performance. Herein, we propose a molecular-extrusion-driven passivation strategy by introducing bromomethyl-triphenylphosphonium bromide (TPB-Br) into perovskite precursors to achieve halogen homogenization. This approach simultaneously passivates bulk and interfacial defects, significantly mitigates phase segregation, and suppresses nonradiative recombination in wide-bandgap perovskites. As a result, we realize high-quality wide-bandgap perovskite films with high crystallinity, low defect density and released residual strain. Champion devices based on these films deliver impressive power conversion efficiencies (PCEs) of 23.63% in the 1.68 eV perovskite sub-cell and 32.03% (1.05 cm2) in the perovskite/silicon tandem solar cell. More importantly, the unencapsulated devices maintained 90.1%, 81.2%, and 93.4% of their initial PCEs under long-term storage, thermal-aging, and light-soaking for 1200 h, respectively. Our work demonstrates the advantage and feasibility of the synergistic passivation strategy in preparing high-quality wide-bandgap perovskite films and tandem solar cells.
AB - Phase segregation is an inevitable phenomenon in wide-bandgap perovskites, triggering nonradiative recombination and degrading device performance. Herein, we propose a molecular-extrusion-driven passivation strategy by introducing bromomethyl-triphenylphosphonium bromide (TPB-Br) into perovskite precursors to achieve halogen homogenization. This approach simultaneously passivates bulk and interfacial defects, significantly mitigates phase segregation, and suppresses nonradiative recombination in wide-bandgap perovskites. As a result, we realize high-quality wide-bandgap perovskite films with high crystallinity, low defect density and released residual strain. Champion devices based on these films deliver impressive power conversion efficiencies (PCEs) of 23.63% in the 1.68 eV perovskite sub-cell and 32.03% (1.05 cm2) in the perovskite/silicon tandem solar cell. More importantly, the unencapsulated devices maintained 90.1%, 81.2%, and 93.4% of their initial PCEs under long-term storage, thermal-aging, and light-soaking for 1200 h, respectively. Our work demonstrates the advantage and feasibility of the synergistic passivation strategy in preparing high-quality wide-bandgap perovskite films and tandem solar cells.
KW - efficiency
KW - molecular extrusion
KW - perovskite/silicon tandem
KW - phase segregation
KW - wide-bandgap perovskite
UR - https://www.scopus.com/pages/publications/105044141480
U2 - 10.1002/anie.5530609
DO - 10.1002/anie.5530609
M3 - Article
AN - SCOPUS:105044141480
SN - 1433-7851
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
ER -