4.8 Article

Synergistic Effect of Co(III) and Co(II) in a 3D Structured Co3O4/Carbon Felt Electrode for Enhanced Electrochemical Nitrate Reduction Reaction

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 24, Pages 28348-28358

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c07063

Keywords

electrochemical nitrate reduction reaction; 3D structure; Co3O4/carbon felt electrode; high-rate nitrate removal; atomic H*; synergistic effect; Co(II)-Co(III)-Co(II) redox cycle

Funding

  1. Tianjin Development Program for Innovation and Entrepreneurship
  2. Natural Science Foundation of China [21773129, 21976096, 21811730274, 21273120]
  3. Tianjin Science and Technology Program [19PTZWHZ00050]
  4. NCC Fund [NCC2020PY15]
  5. Tianjin Post-graduate Students Research and Innovation Project [2019YJSB075, 2020YJSB048]
  6. Fundamental Research Funds for the Central Universities, Nankai University

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The study demonstrates that by controlling the calcination temperature, a relatively large amount of Co(II) on the surface of the Co3O4/CF electrode (1.3 Co(II)/Co(III) ratio) can be maintained to promote H* formation and enhance the performance of the ENRR. Therefore, building a 3D structure and optimizing the Co(II)/Co(III) ratio are crucial for designing efficient Co3O4 electrocatalysts for ENRR.
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 x 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 degrees 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.

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