Lucie Rivet, Antoine Curé, Camille Jutard, Samuel Fauvel, Renaud Demadrille, Antonio J Riquelme, Cyril Aumaître
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引用次数: 0
Abstract
Among the latest advances in organic solar cells, all-polymer solar cells based on non-fullerene acceptors (NFAs) are emerging as a promising way to improve device stability. However, the synthesis of new electron-accepting polymers suitable for the active layer remains relatively unexplored. Current efforts primarily focus on maximizing photovoltaic conversion efficiency using PY-IT, a polymer derived from Y6. By contrast, there is a lack of fundamental research into controlling polymerization processes and the effect of the intrinsic optoelectronic properties of NFA-based polymers on their reactivity and stability when subjected to thermal stress and light soaking. To address this, we present the synthesis of a series of NFA-based polymers that incorporate thiophene, indacenodithiophene or a thienothiophene analogue. We systematically optimized Stille polymerisation by evaluating a range of phosphine ligands and correlating their performance with Tollman electronic and steric parameters, an approach that has rarely been explored in the literature. The resulting polymers exhibit improved macromolecular control, good solubility in o-xylene and optical properties suited to integration into the active layer of solar cells. Comprehensive spectroscopic and morphological characterisation (UV-vis, AFM and GIWAXS) of pristine polymer films confirms their amorphous nature in the solid state. The thermal and photochemical stability of the three new polymers was evaluated in devices under ISOS-D-2 (thermal ageing) and ISOS-L-1 (light soaking) protocols. After 1000 hours of thermal stress, all devices retained over 90% of their initial efficiency and they also demonstrated outstanding photostability over 300 hours under 1 Sun illumination. Some materials showed no degradation under these conditions, highlighting the potential of all-polymer solar cells to overcome long-standing stability challenges in organic photovoltaics.
在有机太阳能电池的最新进展中,基于非富勒烯受体(nfa)的全聚合物太阳能电池正成为提高器件稳定性的一种有前途的方法。然而,适合于活性层的新型电子接受聚合物的合成仍然相对未被探索。目前的努力主要集中在利用PY-IT(一种由Y6衍生的聚合物)最大限度地提高光伏转换效率。相比之下,在控制聚合过程以及nfa基聚合物在热应力和光浸泡下的光电特性对其反应性和稳定性的影响方面缺乏基础研究。为了解决这个问题,我们提出了一系列以nfa为基础的聚合物的合成,这些聚合物含有噻吩、吲哚二噻吩或噻吩类似物。我们通过评估一系列膦配体并将其性能与Tollman电子和立体参数相关联,系统地优化了Stille聚合,这是一种在文献中很少探索的方法。所得聚合物表现出更好的大分子控制,在邻二甲苯中的良好溶解度和适合集成到太阳能电池活性层的光学性能。对原始聚合物薄膜进行了全面的光谱和形态表征(UV-vis, AFM和GIWAXS),证实了它们在固体状态下的无定形性质。在iso - d -2(热老化)和iso - l -1(光浸泡)协议下,对这三种新聚合物的热和光化学稳定性进行了评估。在1000小时的热应力后,所有器件都保持了超过90%的初始效率,并且在1个太阳照射下,它们在300小时内也表现出出色的光稳定性。一些材料在这些条件下没有表现出降解,突出了全聚合物太阳能电池克服有机光伏电池长期存在的稳定性挑战的潜力。
期刊介绍:
The Journal of Materials Chemistry is divided into three distinct sections, A, B, and C, each catering to specific applications of the materials under study:
Journal of Materials Chemistry A focuses primarily on materials intended for applications in energy and sustainability.
Journal of Materials Chemistry B specializes in materials designed for applications in biology and medicine.
Journal of Materials Chemistry C is dedicated to materials suitable for applications in optical, magnetic, and electronic devices.
Example topic areas within the scope of Journal of Materials Chemistry C are listed below. This list is neither exhaustive nor exclusive.
Bioelectronics
Conductors
Detectors
Dielectrics
Displays
Ferroelectrics
Lasers
LEDs
Lighting
Liquid crystals
Memory
Metamaterials
Multiferroics
Photonics
Photovoltaics
Semiconductors
Sensors
Single molecule conductors
Spintronics
Superconductors
Thermoelectrics
Topological insulators
Transistors