Abstract

Electrochemical synthesis of hydrogen peroxide (H2O2) via two-electron oxygen reduction reaction (2e- ORR) or two-electron water oxidation reaction (2e- WOR), parades great prospects in substituting traditional anthraquinone process. However, the low efficiency and selectivity hinders its practical utilization. Exploration of a bifunctional catalyst capable of simultaneously driving the 2e- WOR and 2e- ORR is crucial for thoroughly improving H2O2 conversion efficiency. Herein, by means of first principles calculation, the 2e- ORR and 2e- WOR activities of metal-nitrogen doped carbon (M−NC, M = Mn, Fe, Co, Ni, Ru, In, and Pt) are investigated. Combining the pyrrole nitrogen coordination regulation, the best sample (RuN(Po)4) is screened from forty single atom configurations, which exhibits ultra-low overpotentials (0.02 V/0.04 V) and excellent inhibition on 4e- ORR/WOR side reactions. In-depth study further verifies its low reaction energy barrier and high thermodynamic stability for H2O2 synthesis in two pathways. Our work is expected to provide useful understanding for designing highly-efficient bifunctional catalysts for H2O2 production.

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