Inclusion of polysaccharides in perovskite thin films: from in-solution interaction to film formation and stability†

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Nanoscale Advances Pub Date : 2025-03-11 DOI:10.1039/D4NA01036A
Francesco Bisconti, Antonella Giuri, Nadir Vanni, Sonia Carallo, Silvia Spera, Rosamaria Marrazzo, Riccardo Po', Paolo Biagini, Barbara Paci, Amanda Generosi, Marco Guaragno, Carola Esposito Corcione, Andrea Listorti, Silvia Colella and Aurora Rizzo
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Abstract

Despite perovskite solar cells (PSCs) being among the most promising photovoltaic technologies, their widespread adoption requires further advancements in material processability and long-term stability. Polysaccharides have emerged as effective additives for assisted perovskite thin film crystallization in one step dripping-free deposition. Here, with the aim of rationalising their effect, the role of the hydroxyl groups (–OH) in the polymer structure, affecting the formation of perovskite–polymer nanocomposites, has been thoroughly analysed by comparing two celluloses, hydroxyethyl cellulose (HEC) and cellulose acetate (CAT), in which some of the –OH groups are replaced by acetyl groups. The combination of nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and rheological analysis showed that HEC strongly interacts with perovskite precursors already in solution, retards DMSO evaporation and then modifies the crystallisation dynamics process, resulting in a film characterised by highly uniform grain structure and improved film stability, with a power conversion efficiency (PCE) of 15.89%. In contrast, CAT with partially substituted –OH groups showed weaker interactions resulting in non-uniform crystal growth and poor film morphology. Furthermore, Energy Dispersive X-ray Reflectivity (EDXR), Atomic Force Microscopy (AFM), and X-ray Diffraction (XRD) confirm that HEC-based films maintain structural stability under light-aging conditions, whereas pristine methylammonium lead iodide (MAPbI3) undergoes significant degradation. These findings highlight the potential of HEC as an intrinsic stabilizer for perovskite films, paving the way for more durable and scalable PSC technologies.

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钙钛矿薄膜中多糖的包合:从溶液中相互作用到薄膜的形成和稳定性。
尽管钙钛矿太阳能电池(PSCs)是最有前途的光伏技术之一,但其广泛采用需要进一步提高材料的可加工性和长期稳定性。多糖作为辅助钙钛矿薄膜一步无滴结晶的有效添加剂已被发现。在这里,为了使它们的作用合理化,羟基(-OH)在聚合物结构中的作用,影响钙钛矿-聚合物纳米复合材料的形成,已经通过比较两种纤维素,羟乙基纤维素(HEC)和醋酸纤维素(CAT)进行了彻底的分析,其中一些-OH基团被乙酰基取代。核磁共振(NMR)、差示扫描量热法(DSC)、热重分析(TGA)和流变学分析表明,HEC与溶液中的钙钛矿前驱体强相互作用,延缓DMSO蒸发,进而改变结晶动力学过程,形成晶粒结构高度均匀、膜稳定性提高的薄膜,功率转换效率(PCE)为15.89%。相反,部分取代-OH基团的CAT相互作用较弱,导致晶体生长不均匀,膜形态较差。此外,能量色散x射线反射率(EDXR)、原子力显微镜(AFM)和x射线衍射(XRD)证实,hec基薄膜在光老化条件下保持结构稳定性,而原始甲基碘化铅(MAPbI3)则会发生明显的降解。这些发现突出了HEC作为钙钛矿薄膜固有稳定剂的潜力,为更耐用和可扩展的PSC技术铺平了道路。
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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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