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电子强耦合改变了自组装二氢卟吩分子中的基态分子间相互作用。

Electronic strong coupling modifies the ground-state intermolecular interactions in self-assembled chlorin molecules.

作者信息

Biswas Subha, Mondal Mainak, Chandrasekharan Gokul, Mony Kavya S, Singh Akshay, Thomas Anoop

机构信息

Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bengaluru, 560012, India.

Department of Physics, Indian Institute of Science, Bengaluru, 560012, India.

出版信息

Nat Commun. 2025 Jun 2;16(1):5115. doi: 10.1038/s41467-025-60025-8.

Abstract

The strong coupling of a molecular electronic transition with a quantized radiation field can result in modified photophysics compared to its uncoupled counterparts. Often, such changes are attributed to kinetic factors, overlooking the possible modifications to intermolecular interactions. The spin-cast films of chlorin e6 trimethyl ester (Ce6T) show an excitonic coupling band in absorption resulting from their ground-state intermolecular interactions and subsequent excimer-like emission upon photoexcitation. Interestingly, the electronic strong coupling (ESC) of the Ce6T Soret and Q-band suppresses the intermolecular excitonic interactions that otherwise exist in the Ce6T thin films and brings back the monomer-like emission characteristics. Our experiment provides a unique tool to tune the molecular assembly without involving chemical modifications. Our results suggest that ESC can induce modification to the intermolecular interaction forces that hold together the molecular assemblies in the ground state, which is a significant step toward understanding the fundamentals of polaritonic chemistry in detail.

摘要

与未耦合的同类分子相比,分子电子跃迁与量子化辐射场的强耦合会导致光物理性质发生改变。通常,这种变化归因于动力学因素,而忽略了对分子间相互作用可能产生的改变。二氢卟吩e6三甲酯(Ce6T)的旋涂薄膜在吸收光谱中显示出激子耦合带,这是由其基态分子间相互作用以及光激发后随后的准分子样发射引起的。有趣的是,Ce6T的Soret带和Q带的电子强耦合(ESC)抑制了Ce6T薄膜中原本存在的分子间激子相互作用,并恢复了单体样发射特性。我们的实验提供了一种无需进行化学修饰就能调节分子组装的独特工具。我们的结果表明,ESC可以诱导对基态下将分子组装体维系在一起的分子间相互作用力的改变,这是朝着详细理解极化子化学基本原理迈出的重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63d3/12130188/9fb540ca5b5d/41467_2025_60025_Fig1_HTML.jpg

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