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Abstract
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he catalytic reduction of O2 molecule into H2O is investigated over a P-doped divacancy C3N nanosheet (P-Dv-C3N) by using density functional theory calculations. A negative formation energy is calculated for P-Dv-C3N, suggesting that the introduction of a P atom into divacancy defective C3N would be thermodynamically favorable. The oxygen reduction reaction (ORR) over P-Dv-C3N would proceed via a 4e− pathway (O2 + 4H+ + 4e−→ 2H2O) at room temperature. The rate-determining step of the ORR on P-Dv-C3N is O + H+ + e− → OH which requires an activation energy of 1.21 eV. These results provide helpful insights into design novel metal-free catalysts to improve the kinetics of ORR in fuel cells.
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