Tuning charge dynamics in MIL-88A(Fe) via decoration by boron carbon nitride quantum dots for superior photocatalytic elimination performance
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The development of efficient and sustainable strategies for the removal of pharmaceutical pollutants from aqueous environments has become a critical challenge. Boron carbon nitride quantum dots (BCNQDs) have emerged as highly promising materials in photocatalysis, offering substantial performance advantages. In this study, BCNQDs were successfully integrated onto the MIL-88A(Fe) framework for the first time via a simple impregnation technique. Characterization analyses confirmed that the crystalline integrity and surface functionalities of MIL-88A(Fe) were preserved following BCNQDs decoration. HRTEM images revealed spherical BCNQDs uniformly distributed over the hexagonal rod-like MIL-88A structure. Photoluminescence (PL) and photocurrent analyses demonstrated that the integration of BCNQDs effectively suppressed electron-hole recombination. Moreover, the photocatalytic performance was significantly enhanced, with tetracycline (TC) removal efficiency increasing from 45.09 % for pristine MIL-88A to 95.19 % in the optimized MIL-88A(Fe) @BCNQDs catalyst, alongside a sixfold increase in reaction rate. This improvement was attributed to synergistic effects including enhanced charge separation, extended light absorption, favorable band structure modulation, and improved pollutant-catalyst interactions. The hybrid photocatalyst maintained high degradation efficiencies in various water matrices, achieving 84.1 % and 71.2 % removal in tap water and seawater, respectively. Radical scavenging experiments revealed a hole-dominated photocatalytic pathway, with BCNQDs functioning as efficient electron traps, thereby prolonging hole lifetimes and enabling effective oxidation under visible light. Additionally, the MIL-88A(Fe)@BCNQDs catalyst exhibited excellent reusability, retaining over 70 % efficiency after eight consecutive cycles. Overall, this study pioneers the integration of BCNQDs into a MOFbased photocatalyst, unveiling their untapped potential as next-generation, eco-friendly co-catalysts. The findings not only modulate charge carrier dynamics but also establish a new benchmark for sustainable antibiotic degradation under visible light.









