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Citation: Jingyi Xie,  Qianxi Lü,  Weizhen Qiao,  Chenyu Bu,  Yusheng Zhang,  Xuejun Zhai,  Renqing Lü,  Yongming Chai,  Bin Dong. Enhancing Cobalt―Oxygen Bond to Stabilize Defective Co2MnO4 in Acidic Oxygen Evolution[J]. Acta Physico-Chimica Sinica, ;2024, 40(3): 230502. doi: 10.3866/PKU.WHXB202305021 shu

Enhancing Cobalt―Oxygen Bond to Stabilize Defective Co2MnO4 in Acidic Oxygen Evolution

  • State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, Shandong Province, China

  • Corresponding author: Yongming Chai,  Bin Dong, 
  • Received Date: 9 May 2023
    Revised Date: 8 July 2023
    Accepted Date: 10 July 2023

    Fund Project: The project was supported by the National Natural Science Foundation of China (52174283), Innovation Fund Project for Graduate Student of China University of Petroleum (East China) (22CX04023A), and the Fundamental Research Funds for the Central Universities.

  • Co-based oxides have shown promise as catalysts for the oxygen evolution reaction (OER), as evidenced by experimental and theoretical studies. However, these common Co-based catalysts suffer from poor stability in acidic environments, making them susceptible to corrosion in acid electrolytes. Consequently, developing OER catalysts that can maintain both activity and stability under strongly acidic conditions is a challenging task for large-scale industrial hydrogen production applications. To address this challenge, the incorporation of manganese (Mn) into the spinel lattice of Co3O4 (CoMn1O) has been proposed, resulting in a defect-rich catalyst with improved lifetime in acidic electrolytes. The crystalline phase structures and chemical valence states were investigated using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM), and energy-dispersive spectroscopy (EDS) elemental maps. The introduction of Mn led to the generation of a significant number of defects due to changes in the local crystal structure. Additionally, as the amount of Mn atoms increased, a red shift was observed in the Co 2p spectrum, indicating an increase in the overall valence of Co and the formation of more stable Co―O bonds. Moreover, when the Mn-to-Co ratio reached 1 (CoMn1O), the resulting catalyst exhibited promising OER activity, with overpotentials of 415 and 552 mV at 10 and 50 mA·cm-2, respectively. Detailed physical characterization and electrochemical tests demonstrated that CoMn1O exhibited over four times the stability of Mn-free Co3O4 (CoMn0O). This enhanced stability can be attributed to the introduction of Mn, which promotes electron density bias of Co towards O, resulting in the formation of more stable Co―O bonds. Mn also facilitates acidic oxygen evolution by delaying the oxidation rate of the Co active sites, thereby enhancing stability. Density functional theory (DFT) calculations were further employed to analyze the electronic structures of CoMn1O and CoMn0O. The d-band center of Co 3d (εd) in CoMn1O shifted closer to the Fermi level (EF) compared to that of CoMn0O, indicating a reduced reaction energy barrier for CoMn1O and enhanced bonding interaction with OER intermediates. Overall, this work presents a promising strategy for achieving highly efficient and stable acidic oxygen evolution using noble-metal-free electrocatalysts.
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