Abstract
Carbon-based CsPbI3 perovskite solar cells (C-PSCs) have exhibited great application potential because of their suitable optical bandgap and high chemical stability. However, the efficiency of CsPbI3 C-PSCs still lags behind the theoretical limits, mainly because of issues such as high defect density, non-ideal energy level alignment, and susceptibility to humidity or thermal stress. Herein, a multifunctional molecule, S-benzylisothiourea hydrochloride (BSH), is introduced to modify CsPbI3 perovskite films. It is demonstrated that the BSH treatment can enhance moisture resistance and enable BSH+ to react with residual PbI2, forming a low-dimensional (BSH)2PbX4 structure that passivates surface defects and improves energy-level alignment at the CsPbI3/carbon interface. Concurrently, Cl− distributes throughout the surface and buried interface, facilitating film reconstruction and passivating defects at both the surface and the TiO2/perovskite interface. The optimized devices achieve a PCE of 18.03% with a fill factor of 80.94%, along with enhanced stability, retaining 76.65% of initial PCE after 320 h at 85 °C in 20-30% RH and 88.73% after 1350 h at 25 °C in 20-30% RH.
| Original language | English |
|---|---|
| Article number | 240463 |
| Journal | Journal of Power Sources |
| Volume | 684 |
| DOIs | |
| State | Published - 30 Aug 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Carbon electrode
- CsPbI
- Defect passivation
- Inorganic perovskite
- Interfacial modification
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