Abstract
Precisely tailoring the nitrogen defects has been verified to be a promising approach for promoting the photocatalytic efficiency of C3N4. Herein, two-coordinated-N vacancies are selectively introduced into the C3N4 framework by a facile Cl- modification method, whereas its concentration can be facilely tuned by varying Cl- usage in the process of thermal polymerization. Impressively, the optimal defective C3N4 (20 mg) exhibited superior hydrogen and oxygen evolution rates of 48.2 and 21.8 μmol h-1, respectively, in photocatalytic overall water splitting and an apparent quantum efficiency of 6.9% at 420 nm, the highest of reported single-component C3N4 photocatalysts for overall water splitting. Systematic studies including XPS, DFT simulations, and NEXAFS reveal that Cl- modification preferentially facilitates the introduction of two-coordinated-N vacancies through tuning the formation energy and promotes charge carrier separation efficiency, thereby greatly enhancing the photocatalytic efficiency. This work allows for a viable approach to rationally designing defective C3N4 for efficient photocatalysis.
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