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静电相互作用与π-π相互作用在纳米级人工光合模型系统实现中的协同作用

Synergy of Electrostatic and π-π Interactions in the Realization of Nanoscale Artificial Photosynthetic Model Systems.

作者信息

Anaya-Plaza Eduardo, Joseph Jan, Bauroth Stefan, Wagner Maximilian, Dolle Christian, Sekita Michael, Gröhn Franziska, Spiecker Erdmann, Clark Timothy, de la Escosura Andrés, Guldi Dirk M, Torres Tomás

机构信息

Department of Organic Chemistry, Universidad Autónoma de Madrid (UAM), c/ Francisco Tomás y Valiente 7, Cantoblanco, 28049, Madrid, Spain.

Department of Bioproducts and Biosystems, Aalto University, Kemistintie 1, 02150, Espoo, Finland.

出版信息

Angew Chem Int Ed Engl. 2020 Oct 12;59(42):18786-18794. doi: 10.1002/anie.202006014. Epub 2020 Sep 2.

Abstract

In the scientific race to build up photoactive electron donor-acceptor systems with increasing efficiencies, little is known about the interplay of their building blocks when integrated into supramolecular nanoscale arrays, particularly in aqueous environments. Here, we describe an aqueous donor-acceptor ensemble whose emergence as a nanoscale material renders it remarkably stable and efficient. We have focused on a tetracationic zinc phthalocyanine (ZnPc) featuring pyrenes, which shows an unprecedented mode of aggregation, driven by subtle cooperation between electrostatic and π-π interactions. Our studies demonstrate monocrystalline growth in solution and a symmetry-breaking intermolecular charge transfer between adjacent ZnPcs upon photoexcitation. Immobilizing a negatively charged fullerene (C ) as electron acceptor onto the monocrystalline ZnPc assemblies was found to enhance the overall stability, and to suppress the energy-wasting charge recombination found in the absence of C . Overall, the resulting artificial photosynthetic model system exhibits a high degree of preorganization, which facilitates efficient charge separation and subsequent charge transport.

摘要

在构建效率不断提高的光活性电子供体 - 受体系统的科学竞赛中,对于这些构建模块集成到超分子纳米级阵列中时,尤其是在水性环境中的相互作用,人们了解甚少。在此,我们描述了一种水性供体 - 受体组合,其作为纳米级材料的出现使其具有显著的稳定性和高效性。我们聚焦于一种带有芘的四价阳离子锌酞菁(ZnPc),它展现出一种前所未有的聚集模式,这种模式由静电相互作用和π - π相互作用之间的微妙协同驱动。我们的研究表明在溶液中会发生单晶生长,并且光激发时相邻ZnPc之间会发生对称性破缺的分子间电荷转移。将带负电荷的富勒烯(C)作为电子受体固定在单晶ZnPc组件上,发现这会增强整体稳定性,并抑制在没有C时出现的能量浪费型电荷复合。总体而言,由此产生的人工光合模型系统展现出高度的预组织性,这有利于高效的电荷分离及随后的电荷传输。

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