Department of Chemistry and Pharmacy and Interdisciplinary Center for Molecular Materials, Friedrich-Alexander-University Erlangen-Nuremberg, 91058 Erlangen, Germany.
Nanoscale. 2015 Mar 19;7(13):5674-82. doi: 10.1039/c4nr05719h.
We describe herein the preparation of novel exfoliated graphene-phthalocyanine nanohybrids, and the investigation of their photophysical properties. Pyridyl-phthalocyanines (Pcs) are presented as novel electron accepting building blocks of variable strengths with great potential for the exfoliation of graphite via their immobilization onto the basal plane of graphene in dimethylformamide (DMF) affording single layered and turbostratic graphene based . were fully characterized (AFM, TEM, Raman, steady-state and pump probe transient absorption spectroscopy) and were studied in terms of electron donor-acceptor interactions in the ground and excited states. In this context, electron transfer upon photoexcitation from graphene to the electron accepting Pcs with dynamics, for example, in of <1 and 330 ± 50 ps for charge separation and charge recombination, respectively, was corroborated in a series of steady-state and time-resolved spectroscopy experiments.
我们在此描述了新型剥离氧化石墨烯酞菁纳米杂化物的制备及其光物理性质的研究。吡啶酞菁(Pcs)作为新型电子接受体构建块,具有很强的可变性,通过在二甲基甲酰胺(DMF)中将其固定在氧化石墨烯的基面上来剥离石墨,从而得到单层和乱层氧化石墨烯基。进行了充分的表征(AFM、TEM、拉曼、稳态和泵浦探测瞬态吸收光谱),并研究了它们在基态和激发态中电子给体-受体相互作用。在这种情况下,通过从氧化石墨烯到电子接受体 Pcs 的光激发进行电子转移,例如,在<1 和 330 ± 50 ps 之间,分别用于电荷分离和电荷复合,这在一系列稳态和时间分辨光谱实验中得到了证实。