Vacuum-Deposited Passivation Layer Boosts Perovskite Solar Cell Performance
Abstract Controlling the top perovskite/electron-transport-layer interface is essential, as it dominates the loss pathways limiting efficiency and reproducibility in inverted perovskite solar cells. Through a systematic comparative study of organic ammonium passivators, we identify vacuum-deposited piperazinium diiodide (PDI-Vac) as an effective route for regulating the perovskite/C60 interfacial organization, enabled by its favorable kinetic and thermodynamic volatility. This approach forms a conformal and homogeneous passivation layer, which significantly reduces trap-assisted non-radiative recombination losses, as evidenced by enhanced photoluminescence, increased photoluminescence quantum yield, prolonged carrier lifetimes, and reduced quasi-Fermi level splitting and associated energy losses. Consequently, PDI-Vac devices achieve a power conversion efficiency (PCE) of 26.05% with markedly improved device-to-device consistency. The benefits persist in wide-bandgap (1.68 eV) perovskites and extend to monolithic perovskite/silicon tandem cells, delivering a PCE of 33.37% (certified 33.09%). The PDI-Vac strategy can serve as a key contributor to a scalable pathway toward commercial viability, delivering reproducible, state-of-the-art performance in perovskite-based photovoltaics. How passivation molecules are arranged at the surface of a perovskite solar cell (PSC) can affect both energy loss and device-to-device consistency. Researchers at UNIST have found that molecular volatility can be used to control this process through vacuum deposition, producing a more uniform interface and more consistent device performance. A research team, led by Professors Changduk Yang of the School of Energy and Chemical Engineering and Kyoung Jin Choi of the Department of Materials Science and Engineering identified piperazinium diiodide (PDI) as particularly well suited to vacuum deposition. The material forms a thin, uniform passivation layer at the perovskite/C60 interface, suppressing defects that would otherwise contribute to energy loss. Passivation materials are typically applied from solution, but uneven molecular adsorption and assembly can create variations across the interface and increase non-radiative recombination. Rather than simply testing different passivators for their ability to suppress defects, the researchers examined molecular volatility as a design parameter for vacuum deposition. After comparing six organic ammonium passivators, the team found that PDI offered a favorable balance of thermal stability and volatility. Deposited at 0.01 nanometers per second, PDI formed a conformal, homogeneous layer at the perovskite/C60 interface, reducing trap-assisted non-radiative recombination. Inverted PSCs using vacuum-deposited PDI reached a power conversion efficiency of 26.05%, compared with 25.43% for cells treated with PDI from solution. Tests across 12 devices also showed less variation in efficiency, indicating improved device consistency. The strategy also proved effective in wide-bandgap perovskites used for perovskite/silicon tandem solar cells. The tandem devices reached 33.37% efficiency, with a certified efficiency of 33.09%. Stability improved as well. Under continuous illumination at 65 °C, cells treated with vacuum-deposited PDI retained 90% of their initial efficiency for 1,005 hours—about 55% longer than cells treated with PDI from solution. “By treating molecular volatility as a design parameter, we were able to precisely control the deposition process and form a uniform passivation layer on the perovskite surface,” said Jeewon Park, a co-first author of the study. “This approach improves efficiency and stability while also reducing performance variation between devices,” said Professor Yang. “Achieving a certified efficiency above 33% in a perovskite/silicon tandem cell demonstrates its potential for producing high-performance solar cells with greater consistency.” Jeewon Park and Jieun Kim of the Department of Energy and Chemical Engineering and Young Im Noh of the Department of Materials Science and Engineering served as co-first authors of the study. Their findings were published in Energy & Environmental Science on September 1, 2026. The research was supported by the National Research Foundation of Korea (NRF), the Korea Institute of Energy Technology Evaluation and Planning (KETEP), and the Ministry of Climate, Energy and Environment (MCEE). Journal Reference Jeewon Park, Jieun Kim, Young Im Noh, et al ., “Volatility-governed interfacial organization for low-loss perovskite tandems,” Energy Environ. Sci. , (2026).
2026.10.13