材料科学
钙钛矿(结构)
介观物理学
制作
纳米技术
光电子学
工程物理
化学工程
凝聚态物理
医学
物理
工程类
病理
替代医学
作者
Qin Zeng,Yiwen Chen,Weihuang Yang,Zheling Zhang,Wenfeng Liu,Yang Zhang,Yu Huang,Dongjie Wang,Qiaogan Liao,Jian Zhang
标识
DOI:10.1021/acsami.5c04888
摘要
In printable mesoporous perovskite solar cells (p-MPSCs), the perovskite films deposited from room-temperature solvents can effectively optimize the interface between the perovskite films and the electrodes. However, the low crystallization rate of perovskite thin films at room temperature often leads to the formation of nonphotoactive phases and an increase in the density of defect states. To accelerate the crystallization of perovskite films at room temperature, acetonitrile (ACN) is introduced as a cosolvent in the binary solvent system of 2-methoxyethanol/N-methyl-2-pyrrolidone (2 ME/NMP). The high volatility and excellent wettability of ACN improve the crystallization rate of perovskite films and optimize their crystallinity. Furthermore, the introduction of the multifunctional additive Phenformin hydrochloride in the perovskite precursor solution further optimizes the crystallization process of the perovskite films, passivating deep defects in the perovskite films and forming high-quality perovskite films in the mesopores. The optimized p-MPSCs achieve a power conversion efficiency (PCE) of 18.30%, which is the highest PCE for room temperature perovskite film p-MPSCs. Moreover, the optimized p-MPSCs exhibit negligible hysteresis and excellent reproducibility, showing no significant PCE degradation after being stored in air for over 3000 h.
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