Synergistic Effect of Co(III) and Co(II) in a 3D Structured Co<sub>3</sub>O<sub>4</sub>/Carbon Felt Electrode for Enhanced Electrochemical Nitrate Reduction Reaction
Wenyang Fu, Xuedong Du, Pei Su, Qizhan Zhang, Minghua Zhou
Abstract
As nitrate contamination causes serious environmental problems, it is necessary to develop stable and efficient electrocatalysts for efficient electrochemical nitrate reduction reaction (ENRR). Here, a nonprecious Co3O4/carbon felt (CF) electrode with a 3D structure was prepared by integrating electrodeposition with calcination methods. This 3D structured Co3O4/CF electrode exhibits a high-rate constant of 1.18 × 10–4 s–1 cm–2 for the ENRR, surpassing other Co3O4 electrodes in previous literature. Moreover, it also has an excellent stability with a decrease of 6.4% after 10 cycles. Density functional theory calculations, electron spin resonance analysis, and cyclic voltammetry were performed to study the mechanism of the ENRR on the Co3O4/CF electrode, proving that atomic H* (indirect pathway) plays a prominent role in NO3– reduction and clarifying the synergistic effect of Co(III) and Co(II) in the Co(II)–Co(III)–Co(II) redox cycle for the ENRR: Co(III) prefers the adsorption of NO3– and Co(II) favors the production of H*. Based on this synergy, a relatively large amounts of Co(II) on the surface of the Co3O4/CF electrode (1.3 Co(II)/Co(III) ratio) was maintained by controlling the temperature of calcination to 200 °C with a lower energy barrier of H* formation of 0.46 eV than other ratios, which is beneficial for forming H* and enhancing the performance of the ENRR. Thus, this study suggests that building 3D structure and optimizing Co(II)/Co(III) ratio are important for designing efficient Co3O4 electrocatalyst for ENRR.