Experimental investigation of light-driven properties in porphyrin-graphene hybrids, indicating potential for advanced applications.
The noncovalent interactions between meso‐tetra(4‐sulfonatophenyl)porphyrin (TPPS) and graphene‐based materials, including graphene oxide (GO), reduced GO (RGO), and RGO modified with Pluronic P123 (RGO‐P123), were systematically investigated. These types of hybrid nanostructures are of significant interest for various applications, including photocatalysis or biomedical applications, due to their ability to enhance light‐driven processes and improve the efficiency of drug delivery. Absorption, emission, femtosecond transient absorption, and nanosecond transient absorption spectroscopy, along with structural analyses, demonstrated that TPPS interacts more strongly with RGO than with GO. This is attributed to enhanced π–π stacking interactions between the porphyrin macrocycle and the highly conjugated surface of RGO. The presence of Pluronic 123 in the TPPS‐RGO system led to an improvement in dispersion stability, which is a critical factor for maintaining the long‐term functionality of these materials. The study provides insights into the fundamental aspects of noncovalent interactions in porphyrin‐graphene systems, highlighting their potential for designing advanced materials with tailored photocatalytic and biomedical properties.
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Lesniewicz et al. (2026) studied this question.
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