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Updated: Sep 16, 2025

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Synergistic Efficiency-Stability Enhancement in Sn-Pb Narrow-Bandgap Perovskite Solar Cells via Molecular
Yibin Lai1, Xuehui Xu1,2, Pan Li1
1State Key Laboratory of Extreme Photonics and Instrumentation, College of Optical Science and Engineering, Zhejiang University, Hangzhou, Zhejiang, 310027, China.
Abstract:
Tin-lead (Sn-Pb) mixed narrow band gap (NBG) perovskite solar cells (PSCs) hold promise for tandem photovoltaic applications due to their tunable bandgap (≈1.25 eV), but face challenges from rapid crystallization kinetics and operational instability. Conventional ammonium salt passivators improve efficiency but often compromise stability by introducing mobile ions. Herein, alkylammonium halide salts are systematically investigated with varying carbon chain lengths to reconcile this trade-off. As a result, it is found that the long-chain oleylammonium iodide (OAmI) achieves unprecedented synergy. It demonstrates superior defect passivation, enhanced crystallographic orientation, and suppressed ion migration. Transient ion current measurements reveal a fourfold reduction in mobile ion density for OAmI-treated devices. Electrostatic potential calculations and XPS analysis confirm stronger coordination between OAmI and undercoordinated Sn2+/Pb2+ sites, while GIWAXS reveal improved (001)-oriented crystallization and reduced surface roughness. These synergies yield a champion power conversion efficiency (PCE) of 22.69% for gas-quenching produced Sn-Pb PSCs and 14.46% for 6 × 6 cm2 mini-modules, alongside a T80 lifetime nearly twofold increase compared to the control group.
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