Molecular contacts with an orthogonal π-skeleton induce amorphization to enhance perovskite solar cell performance

IF 19.2 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jingjing Zhou, Yixin Luo, Runda Li, Liuwen Tian, Ke Zhao, Jiahui Shen, Donger Jin, Zixuan Peng, Libing Yao, Li Zhang, Qingqing Liu, Shaochen Zhang, Lu Jin, Shenglong Chu, Sisi Wang, Yuan Tian, Jiazhe Xu, Xu Zhang, Pengju Shi, Xiaonan Wang, Wei Fan, Xuechun Sun, Jingyi Sun, Luo-Zhou Chen, Gang Wu, Wen Shi, Hong-Fei Wang, Tianqi Deng, Rui Wang, Deren Yang, Jingjing Xue
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Abstract

Perovskite solar cells represent a promising class of photovoltaics that have achieved exceptional levels of performance within a short time. Such high efficiencies often depend on the use of molecule-based selective contacts that form highly ordered molecular assemblies. Although this high degree of ordering usually benefits charge-carrier transport, it is disrupted by structure deformation and phase transformation when subjected to external stresses, which limits the long-term operational stability of perovskite solar cells. Here we demonstrate a molecular contact with an orthogonal π-skeleton that shows better resilience to external stimuli than commonly used conjugated cores. This molecular design yields a disordered, amorphous structure that is not only highly stable but also demonstrates exceptional charge selectivity and transport capability. The perovskite solar cells fabricated with this orthogonal π-skeleton molecule exhibited enhanced long-term durability in accelerated-ageing tests. This orthogonal π-skeleton functionality opens new opportunities in molecular design for applications in organic electronics. Perovskite solar cells often rely on ordered molecular contacts for favourable charge-carrier transport, and any organizational disruption reduces device efficiency. Now a contact featuring an orthogonal π-skeleton has been shown to afford a high resilience to external stimuli plus long-term durability in accelerated-ageing tests.

Abstract Image

Abstract Image

正交π骨架的分子接触诱导非晶化以提高钙钛矿太阳能电池的性能
钙钛矿太阳能电池代表了一种很有前途的光伏电池,它在短时间内实现了卓越的性能水平。如此高的效率往往依赖于基于分子的选择性接触,形成高度有序的分子组装。虽然这种高度的有序通常有利于电荷载流子的传输,但当受到外部应力时,它会被结构变形和相变所破坏,这限制了钙钛矿太阳能电池的长期运行稳定性。在这里,我们展示了一个分子接触与正交π-骨架,表现出更好的弹性外部刺激比常用的共轭核。这种分子设计产生了一种无序的无定形结构,不仅高度稳定,而且表现出卓越的电荷选择性和传输能力。用该正交π-骨架分子制备的钙钛矿太阳能电池在加速老化试验中表现出较好的长期耐久性。这种正交π-骨架功能为有机电子学中的分子设计应用开辟了新的机会。
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来源期刊
Nature chemistry
Nature chemistry 化学-化学综合
CiteScore
29.60
自引率
1.40%
发文量
226
审稿时长
1.7 months
期刊介绍: Nature Chemistry is a monthly journal that publishes groundbreaking and significant research in all areas of chemistry. It covers traditional subjects such as analytical, inorganic, organic, and physical chemistry, as well as a wide range of other topics including catalysis, computational and theoretical chemistry, and environmental chemistry. The journal also features interdisciplinary research at the interface of chemistry with biology, materials science, nanotechnology, and physics. Manuscripts detailing such multidisciplinary work are encouraged, as long as the central theme pertains to chemistry. Aside from primary research, Nature Chemistry publishes review articles, news and views, research highlights from other journals, commentaries, book reviews, correspondence, and analysis of the broader chemical landscape. It also addresses crucial issues related to education, funding, policy, intellectual property, and the societal impact of chemistry. Nature Chemistry is dedicated to ensuring the highest standards of original research through a fair and rigorous review process. It offers authors maximum visibility for their papers, access to a broad readership, exceptional copy editing and production standards, rapid publication, and independence from academic societies and other vested interests. Overall, Nature Chemistry aims to be the authoritative voice of the global chemical community.
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