Cerdá Jesús, Ortí Enrique, Beljonne David, Aragó Juan
Laboratory for Chemistry of Novel Materials, University of Mons, Mons 7000, Belgium.
Instituto de Ciencia Molecular (ICMol), Universitat de València, Catedrático José Beltrán 2, Paterna 46980, Spain.
J Phys Chem Lett. 2024 Aug 1;15(30):7814-7821. doi: 10.1021/acs.jpclett.4c01520. Epub 2024 Jul 25.
H-bonded -heterotriangulene (NHT) supramolecular polymers offer a nice playground to explore the nature and dynamics of electronic excitations in low-dimensional organic nanostructures. Here, we report on a comprehensive molecular modeling of the excited-state electronic structure and optical properties of model NHT stacks, highlighting the important role of intermolecular charge-transfer (CT) excitations in shaping their optical absorption and emission lineshapes. Most importantly, we show that the coupling between the local and CT excitations, modulated by the electric fields induced by the presence of polar amide groups forming H-bonded arrays along the stacks, significantly increases the resulting hybrid exciton bandwidth. We discuss these findings in the context of the efficient transport of singlet excitons over the μm length scale reported experimentally on individual self-assembled nanofibers with molecular-scale diameter.
氢键连接的 - 异三蝶烯(NHT)超分子聚合物为探索低维有机纳米结构中电子激发的性质和动力学提供了一个很好的平台。在此,我们报告了模型NHT堆叠的激发态电子结构和光学性质的全面分子建模,突出了分子间电荷转移(CT)激发在塑造其光吸收和发射线形中的重要作用。最重要的是,我们表明,由沿着堆叠形成氢键阵列的极性酰胺基团的存在所诱导的电场调制的局部和CT激发之间的耦合,显著增加了所得混合激子带宽。我们在实验报道的具有分子尺度直径的单个自组装纳米纤维上,在微米长度尺度上高效传输单线态激子的背景下讨论这些发现。