Eisenkolb Jasmin, Lloret Vicent, Zink-Lorre Nathalie, Pla Sara, Abellán Gonzalo, Sastre-Santos Ángela, Hauke Frank, Fernández-Lázaro Fernando, Hirsch Andreas
Chair of Organic Chemistry II, Center of Advanced Materials and Processes (ZMP), Friedrich-Alexander University Erlangen-Nürnberg, Dr.-Mack-Str. 81, 90762, Fürth.
Área de Química Orgánica, Instituto de Bioingeniería, Universidad Miguel Hernández, Avda. de la Universidad s/n, 03203, Elche, Spain.
Chemistry. 2024 Dec 2;30(67):e202402166. doi: 10.1002/chem.202402166. Epub 2024 Oct 29.
The non-covalent functionalization of black phosphorus (BP) was studied with a scope of ten tailor-made perylene diimides (PDIs). A combination of UV/Vis-, fluorescence-, as well as Raman spectroscopy and atomic force microscopy was used to investigate the structural factors, which contribute to a pronounced PDI-BP interaction and thus support the protection of BP nanosheets against oxidative degradation. We were able to show, that water-soluble, amphiphilic PDIs with highly charged head groups can be used for the non-covalent functionalization of BP in aqueous media. Here, based on the hydrophobic effect, an efficient adsorption of the respective PDI molecules takes place and leads to the formation of a passivating film, yielding a considerable stabilization of the BP flakes under ambient conditions exceeding 30 days.
研究了十种定制的苝二酰亚胺(PDI)对黑磷(BP)的非共价功能化。结合紫外可见光谱、荧光光谱、拉曼光谱以及原子力显微镜来研究结构因素,这些因素有助于显著的PDI-BP相互作用,从而支持保护BP纳米片免受氧化降解。我们能够证明,具有高电荷头部基团的水溶性两亲性PDI可用于在水性介质中对BP进行非共价功能化。在此,基于疏水效应,相应的PDI分子发生有效吸附并导致形成钝化膜,在超过30天的环境条件下使BP薄片得到相当程度的稳定。