甲脒
三碘化物
钙钛矿(结构)
沉积(地质)
溶剂
化学工程
材料科学
铅(地质)
化学
纳米技术
无机化学
有机化学
物理化学
地质学
色素敏化染料
工程类
古生物学
电极
地貌学
沉积物
电解质
作者
Henry J. Snaith,Benjamin Gallant,Philippe Holzhey,Karim A. Elmestekawy,James Ball,M. Greyson Christoforo,Laura M. Herz,Saqlain Choudhary,Joel A. Smith,Pietro Caprioglio,Igal Levine,Dominik J. Kubicki,Alexandra A. Sheader,Fengning Yang,Daniel T. W. Toolan,Rachel C. Kilbride,Karl‐Augustin Zaininger,Nakita K. Noel
出处
期刊:Research Square - Research Square
日期:2024-09-30
标识
DOI:10.21203/rs.3.rs-1135857/v1
摘要
Abstract Perovskite solar cells (PSCs) offer an efficient, inexpensive alternative to current photovoltaic technologies, with the potential for manufacture via high-throughput coating methods. However, challenges for commercial-scale solution-processing of metal-halide perovskites include the use of harmful solvents, the expense of maintaining controlled atmospheric conditions, and the inherent instabilities of PSCs under operation. Here, we address these challenges by introducing a high volatility, low toxicity, biorenewable solvent system to fabricate a range of 2D perovskites, which we use as highly effective precursor phases for subsequent transformation to α-formamidinium lead triiodide (α-FAPbI3), fully processed under ambient conditions. PSCs utilising our α-FAPbI3 reproducibly show remarkable stability under illumination and elevated temperature (ISOS-L-2) and “damp heat” (ISOS-D-3) stressing, surpassing other state-of-the-art perovskite compositions. We determine that this enhancement is a consequence of the 2D precursor phase crystallisation route, which simultaneously avoids retention of residual low-volatility solvents (such as DMF and DMSO) and reduces the rate of degradation of FA+ in the material. Our findings highlight both the critical role of the initial crystallisation process in determining the operational stability of perovskite materials, and that neat FA+-based perovskites can be competitively stable despite the inherent metastability of the α-phase.
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