材料科学
钙钛矿(结构)
能量转换效率
光伏
成核
化学工程
锡
氧化锡
光伏系统
卤化物
氧化物
钝化
钙钛矿太阳能电池
化学浴沉积
纳米技术
热稳定性
太阳能电池
光电子学
杂质
介孔材料
沉积(地质)
作者
Xin Wang,Ziang Pan,Jingyao Feng,Lifei Chen,Yuchen Song,Wenkai Liao,Peng Huang,Yifan Li,Jianguang Xu,Feng Wang,Xiaoming Zhao
摘要
ABSTRACT SnO 2 is a benchmark electron transport material for perovskite solar cells (PSCs). However, SnO 2 films from the conventional chemical bath deposition (CBD) are limited by impurities and defects that accelerate non‐radiative recombination and compromise device stability. Here, we present a volatile additive engineering strategy using pyruvic acid (PA) as a dual‐functional nucleation promoter and surface modulator during SnO 2 deposition. Owing to its volatility (sublimation at 145°C), PA can be effectively removed during annealing, resulting in cleaner SnO 2 surfaces with reduced residual groups. This is accompanied by a decrease in oxygen‐related defect densities in the SnO 2 layer. This improvement leads to enhanced charge recombination and improved thermal stability at the buried interface. Consequently, PA‐engineered PSCs achieve a power conversion efficiency of 26.17%, together with improved device stability, retaining >80% of their initial efficiency after 900 h of continuous operation, 1000 h at 65°C, and 30 days under 30% relative humidity. Furthermore, this approach is compatible with large‐area fabrication, yielding efficiencies of 24.83% for 1 cm 2 lab‐scale cells and 20.21% for 30 cm × 30 cm industrial‐scale solar modules. These results suggest that controlling additive volatility improves CBD‐SnO 2 quality and offers a promising route for stable, scalable perovskite solar cells.
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