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控制表面光活性:π共轭在半导体表面上酸酐功能化分子中的影响。

Controlling On-Surface Photoactivity: The Impact of π-Conjugation in Anhydride-Functionalized Molecules on a Semiconductor Surface.

作者信息

Frezza Federico, Sánchez-Grande Ana, Canola Sofia, Lamancová Anna, Mutombo Pingo, Chen Qifan, Wäckerlin Christian, Ernst Karl-Heinz, Muntwiler Matthias, Zema Nicola, Di Giovannantonio Marco, Nachtigallová Dana, Jelínek Pavel

机构信息

Institute of Physics, Czech Academy of Sciences, Cukrovarnická 10, 16200, Prague 6, Czech Republic.

Faculty of Nuclear Sciences and Physical Engineering, Czech Technical University in Prague, Břehová 78/7, 11519, Prague 1, Czech Republic.

出版信息

Angew Chem Int Ed Engl. 2024 Jul 22;63(30):e202405983. doi: 10.1002/anie.202405983. Epub 2024 Jun 17.

DOI:10.1002/anie.202405983
PMID:38699982
Abstract

On-surface synthesis has become a prominent method for growing low-dimensional carbon-based nanomaterials on metal surfaces. However, the necessity of decoupling organic nanostructures from metal substrates to exploit their properties requires either transfer methods or new strategies to perform reactions directly on inert surfaces. The use of on-surface light-induced reactions directly on semiconductor/insulating surfaces represents an alternative approach to address these challenges. Here, exploring the photochemical activity of different organic molecules on a SnSe semiconductor surface under ultra-high vacuum, we present a novel on-surface light-induced reaction. The selective photodissociation of the anhydride group is observed, releasing CO and CO. Moreover, we rationalize the relationship between the photochemical activity and the π-conjugation of the molecular core. The different experimental behaviour of two model anhydrides was elucidated by theoretical calculations, showing how the molecular structure influences the distribution of the excited states. Our findings open new pathways for on-surface synthesis directly on technologically relevant substrates.

摘要

表面合成已成为在金属表面生长低维碳基纳米材料的一种突出方法。然而,要将有机纳米结构与金属基底分离以利用其性质,就需要转移方法或新策略来直接在惰性表面上进行反应。直接在半导体/绝缘表面上使用表面光诱导反应是应对这些挑战的一种替代方法。在这里,我们在超高真空下探索不同有机分子在SnSe半导体表面的光化学活性,提出了一种新型的表面光诱导反应。观察到酸酐基团的选择性光解离,释放出CO和CO。此外,我们阐明了光化学活性与分子核心的π共轭之间的关系。通过理论计算阐明了两种模型酸酐不同的实验行为,展示了分子结构如何影响激发态的分布。我们的研究结果为直接在技术相关基底上进行表面合成开辟了新途径。

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