材料科学
退火(玻璃)
制作
卷到卷处理
薄膜
卤化物
四氢呋喃
化学工程
溶剂
能量转换效率
纳米技术
光电子学
复合材料
无机化学
有机化学
化学
工程类
医学
替代医学
病理
作者
Elena J. Cassella,Emma L. K. Spooner,Joel A. Smith,Timothy Thornber,Mary E. O’Kane,Robert D. J. Oliver,Thomas E. Catley,Saqlain Choudhary,Christopher J. Wood,Deborah B. Hammond,Henry J. Snaith,David G. Lidzey
标识
DOI:10.1002/aenm.202203468
摘要
Abstract High temperature post‐deposition annealing of hybrid lead halide perovskite thin films—typically lasting at least 10 min—dramatically limits the maximum roll‐to‐roll coating speed, which determines solar module manufacturing costs. While several approaches for “annealing‐free” perovskite solar cells (PSCs) have been demonstrated, many are of limited feasibility for scalable fabrication. Here, this work has solvent‐engineered a high vapor pressure solvent mixture of 2‐methoxy ethanol and tetrahydrofuran to deposit highly crystalline perovskite thin‐films at room temperature using gas‐quenching to remove the volatile solvents. Using this approach, this work demonstrates p‐i‐n devices with an annealing‐free MAPbI 3 perovskite layer achieving stabilized power conversion efficiencies (PCEs) of up to 18.0%, compared to 18.4% for devices containing an annealed perovskite layer. This work then explores the deposition of self‐assembled molecules as the hole‐transporting layer without annealing. This work finally combines the methods to create fully annealing‐free devices having stabilized PCEs of up to 17.1%. This represents the state‐of‐the‐art for annealing‐free fabrication of PSCs with a process fully compatible with roll‐to‐roll manufacture.
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