Heterogeneous catalysts with specific metal doping improve dye degradation, suggesting pathways for cleaner water solutions.
The removal of synthetic dyes from industrial effluents remains challenging due to their chemical stability and poor biodegradability. Here we engineer metal-doped carbon dots (CDs) as heterogeneous Fenton-like catalysts and elucidate how dopant identity governs structure–activity relationships and reactive oxygen species (ROS) pathways. Fe-, Cu-, Zn- and Mg-doped CDs were prepared via a one-pot hydrothermal route and comprehensively characterised by TEM, FTIR, XPS and zeta-potential analysis. The resulting nanoparticles displayed narrow size distributions (10.2–15.2 nm) and dopant-dependent surface chemistries and charges. Catalytic tests with methylene blue (MB) and rhodamine B (RB) show that Fe-doped CDs deliver the highest activity toward MB degradation (k = 0.0218 min−1), attributable to efficient Fe2+/Fe3+ redox cycling coupled with hydroxyl-rich surfaces that promote H2O2 activation. Zn-doped CDs achieve complete RB decolourisation under Fenton-like conditions, which we ascribe to their higher surface charge and abundant oxygenated sites that enhance pollutant adsorption and ROS generation. Cu- and Mg-doped CDs exhibit intermediate and dopant-specific performances consistent with their respective redox and adsorption characteristics. Collectively, these results establish clear correlations between dopant chemistry, surface functionality, and ROS formation routes, providing mechanistic guidance for the rational design of carbon-based Fenton catalysts for sustainable water remediation.
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Chen et al. (2025) studied this question.
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