TY - JOUR
T1 - Multi-functional Phase-Changeable Salt for Inverted Perovskite Solar Cells
AU - Chen, Peidong
AU - Ou, Zeping
AU - Gao, Mingyang
AU - Wang, Can
AU - Song, Mingyu
AU - Liu, Lei
AU - Pan, Yi
AU - Gao, Qin
AU - Liu, Zhiping
AU - Wan, Wei
AU - Zhang, Junjie
AU - Shen, Jiahui
AU - Wang, Qiangwei
AU - Xiao, Zeyun
AU - Ouedraogo, Nabonswende Aida Nadege
AU - Chen, Yu
AU - Jiang, Tingming
AU - Wang, Rui
AU - Guo, Haoxuan
AU - Sun, Kuan
N1 - Publisher Copyright:
© 2026 Wiley-VCH GmbH.
PY - 2026/3/20
Y1 - 2026/3/20
N2 - Non-radiative recombination and uncontrolled crystallization at the buried perovskite interface remain key barriers to achieving highly efficient and stable perovskite solar cells (PSCs). Herein, we introduce a multi-functional phase-changeable salt, 2-(diphenylphosphino)ethanaminium tetrafluoroborate (DPPEABF4), as a functional interfacial modulator. DPPEA+ interacts with perovskite precursors (FAI and PbI2) through coordination and hydrogen bonding, suppressing excessive nucleation and reducing nucleation density. During annealing, DPPEABF4 undergoes a reversible solid-to-liquid phase transition that buffers heat transfer, ensuring more uniform heating and slower, more controlled crystallization across the substrate. These effects collectively yield perovskite films with enlarged grains, reduced defect densities, and improved crystallinity. Concurrently, π–π stacking between DPPEA+ and Me-4PACz establishes an interfacial dipole that increases the work function and tunes the energy-level alignment at the buried interface, facilitating efficient hole transport. As a result, the optimized devices achieve a champion power conversion efficiency of 26.52% (certified 26.46%) and retain over 90% of their initial efficiency after more than 2000 h of storage under 30–40% relative humidity. This work provides a new paradigm for designing dynamic interfacial materials for high-performance optoelectronic devices.
AB - Non-radiative recombination and uncontrolled crystallization at the buried perovskite interface remain key barriers to achieving highly efficient and stable perovskite solar cells (PSCs). Herein, we introduce a multi-functional phase-changeable salt, 2-(diphenylphosphino)ethanaminium tetrafluoroborate (DPPEABF4), as a functional interfacial modulator. DPPEA+ interacts with perovskite precursors (FAI and PbI2) through coordination and hydrogen bonding, suppressing excessive nucleation and reducing nucleation density. During annealing, DPPEABF4 undergoes a reversible solid-to-liquid phase transition that buffers heat transfer, ensuring more uniform heating and slower, more controlled crystallization across the substrate. These effects collectively yield perovskite films with enlarged grains, reduced defect densities, and improved crystallinity. Concurrently, π–π stacking between DPPEA+ and Me-4PACz establishes an interfacial dipole that increases the work function and tunes the energy-level alignment at the buried interface, facilitating efficient hole transport. As a result, the optimized devices achieve a champion power conversion efficiency of 26.52% (certified 26.46%) and retain over 90% of their initial efficiency after more than 2000 h of storage under 30–40% relative humidity. This work provides a new paradigm for designing dynamic interfacial materials for high-performance optoelectronic devices.
KW - defect passivation
KW - dipole engineering
KW - functional interfaces
KW - perovskite solar cells
KW - phase-changeable salt
UR - https://www.scopus.com/pages/publications/105031162326
U2 - 10.1002/adma.202520030
DO - 10.1002/adma.202520030
M3 - Article
C2 - 41732875
AN - SCOPUS:105031162326
SN - 0935-9648
VL - 38
JO - Advanced Materials
JF - Advanced Materials
IS - 17
M1 - e20030
ER -