4.8 Article

Interfacial engineering of CoMn2O4/NC induced electronic delocalization boosts electrocatalytic nitrogen oxyanions reduction to ammonia

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 322, Issue -, Pages -

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ELSEVIER
DOI: 10.1016/j.apcatb.2022.122090

Keywords

Electrocatalytic; Ammonia; Nitrate reduction; NC; Coupled

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In this study, a new catalyst was developed for efficient wastewater treatment and high-value ammonia generation. The catalyst exhibited high Faradaic efficiency and yield at specific potentials, and the reaction was promoted by the interface effect. The experimental results and theoretical calculations provided insights into the catalytic mechanism and product formation.
Electrocatalytic nitrate (NO3-) reduction reaction (NO3-RR) is a promising avenue for wastewater treatment and value-added ammonia (NH3) generation. Herein, cobalt manganese spinel nanoparticles embedded in multi-channel carbon fibers (CoMn2O4/NC) to obtain optimal NH3 Faradaic efficiency is 92.4% with a yield rate of 144.5 mmol h-1 g-1 at -0.7 V versus reversible hydrogen electrode (vs. RHE). The interfacial between CoMn2O4 and NC induces the 3d orbital electrons of Co and Mn in less localized states, which promotes *NH3 desorption. Electrochemical in situ Raman spectra and online differential electrochemical mass spectrometry (DEMS) identified the intermediates and products. The theoretical calculation demonstrates that the existence of NC could reduce the free energy difference of the rate-determining step (RDS, 0.42 eV) of NO3-RR, suppressing hydrogen evolution reaction (HER) by enhancing the interaction of *H. Coupled benzyl alcohol oxidation re-action (BOR) with NO2-RR to obtain lower reduction voltage and high value-added anode products.

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