Phenyl-modified carbon nitride nanosheets: Enhanced photocatalytic activity via sonication-assisted exfoliation
Year: 2025
Type: article
Abstract: Semiconductor-based photocatalysis represents a valuable approach for sustainable environmental remediation and the production of clean energy. Polymer semiconductors represent an environmentally friendly, metal-free and low-cost option as a photocatalyst material. Among others, graphitic carbon nitride (g-C 3 N 4 ) is one of the most promising materials due to its excellent chemical and thermal stability, as well as its layered structure that facilitates effective charge separation. However, the performance of bulk graphitic carbon nitride (g-C 3 N 4 ) is often limited by poor visible-light absorption and low specific surface area. In the present study, to address these limitations, phenyl-modified carbon nitride (PhCN) was synthesised and subjected to extended liquid-phase exfoliation via ultrasonication, leading to an increased specific surface area and enhanced exposure of active sites. Compared to its bulk counterpart, the exfoliated PhCN exhibited significantly improved photocatalytic performance, enhanced dye degradation rates for Rhodamine B and Methylene Blue in commercial white LED, confirmed mechanism by scavenger tests, and demonstrated a 1.6-fold increase in hydrogen evolution over the bulk under solar simulator. The improvement in photocatalytic activity in the test reactions is primarily assigned to reduced electron-hole recombination facilitated by structural surface defects. The present study highlights the potential of ultrasonicated PhCN for efficient visible-light-driven photocatalytic applications.
Authors: Saswati Bagchi, Riccardo Corpino, Memet Tursun Abudukade, Marco Altomare, Nicoletta Rusta, Stefania Porcu, Pier Carlo Ricci
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $3,230
Funders: Università degli Studi di Cagliari, Innovative Research Group Project of the National Natural Science Foundation of China, Deutsche Forschungsgemeinschaft, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Ministero dell’Istruzione, dell’Università e della Ricerca, Technische Universität Wien, Ministero dell'Università e della Ricerca, Ministero dell'Istruzione e del Merito
OpenAlex ID: W4416260873
