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Demonstrates enhanced photocatalytic activity in water treatment using a novel hybrid catalyst, indicating improved pollutant degradation.
Functionalized carbon dots (CDs) exhibit intriguing photo-exciton dynamics. CDs can donate or accept electrons depending on their functional groups and electrostatic characteristics. We exploited the electron-accepting capability of nitrogen-doped graphitic carbon dots (N- g -CDs) to improve the charge-carrier separation of the polymeric carbon nitride (PCN) photocatalyst. l -Aspartic acid pyrolyzed at 320 °C yielded ∼25 nm size N- g -CDs that were embedded with PCN. The in-plane infiltration of nanosized N- g -CDs increased the surface area of PCN from 11.5 to 104.9 m 2 g –1 . The N- g -CDs/PCN hybrid catalyst tested for photocatalytic chromium reduction evidenced about a 3-fold higher rate than PCN. Also, the antibiotic tetracycline and rhodamine B dye rapidly degraded with faster degradation kinetics. The carrier dynamic analysis and computational investigations suggest that the electron acceptor feature of N- g -CDs governs the effective separation of photo-excitons and the high surface area of N- g -CDs/PCN contributes to photoactivity enhancement. This study offers insights into designing high-performance metal-free photocatalysts for water treatment applications.
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Bhoyar et al. (2023) studied this question.
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