Enhanced Thermal Stability in Perovskite Solar Cells via the Integration of a Nonionic Binary Compound

초록

Phenethylammonium (PEA+) has been extensively used for defect passivation, enhancing the photovoltaic performance of perovskite solar cells (PSCs) by forming a quasi-2D perovskite layer atop the 3D perovskite. However, the ionic nature of PEA+ renders it prone to deprotonation at elevated temperatures, generating neutral PEA0, which exhibits strong nucleophilicity and easily reacts with formamidinium cations (FA+) in the 3D perovskite. This reaction accelerates perovskite degradation, thereby deteriorating photovoltaic properties and long-term stability. Here, N,N-dimethylbenzenesulfonamide (DMBSA), a nonionic binary compound synthesized via a simple process, is applied as a defect passivation material. Unlike PEA+, DMBSA remains thermally stable due to strong covalent bonding and does not undergo deprotonation at elevated temperatures. Moreover, its lower nucleophilicity prevents undesirable reactions with FA+, significantly mitigating perovskite degradation. Consequently, DMBSA-passivated PSCs maintain 96.1 +/- 0.8% of their initial photoconversion efficiency (PCE) after 1500 h of thermal stress at 85 degrees C, compared to only 64.0 +/- 0.19% for PEA+-passivated PSCs. Furthermore, DMBSA passivation effectively suppresses nonradiative recombination, while its dipole moment induces an electrical field, facilitating efficient hole transfer to the hole transporting layer. As a result, DMBSA-passivated PSC achieves a PCE of 25.43% (certified 25.1%), substantially outperforming pristine PSC (22.07%).

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