Improving the electrocatalytic hydrogen evolution reaction through a magnetic field and hydrogen peroxide production co-assisted Ni/Fe3O4@poly(3,4-ethylene-dioxythiophene)/Ni electrode

• Published in: Journal of colloid and interface science 2024-01, Vol.654, p.1303-1311
• Main Authors: Hou, Zhi-Qiang, Hu, Wen-Ping, Yang, Guo-Hua, Zhang, Zi-Xuan, Cheng, Tian-Yi, Huang, Ke-Jing
• Format: Article
• Language: English
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2023.10.151

The production of high-purity hydrogen using surplus electrical energy and abundant water resources has immense potential in mitigating the fossil energy crisis, as hydrogen fuel holds clean, pollution-free, and high-energy characteristics. However, the practical application of large-scale hydrogen production from water faces challenges such as high overpotentials, sluggish dynamics, and limited electrocatalytic lifetime associated with the hydrogen evolution reaction (HER). Here, we fabricated the sandwich structure of a Ni/Fe3O4@poly(3,4-ethylene-dioxythiophene)/Ni (Ni/Fe3O4@PEDOT/Ni) electrode and employed a strong magnet to obtain a magnetic electrode capable of achieving high-activity and durability for HER. Electrochemical analysis reveals that the activated magnetic electrode displays a significantly reduced overpotential and an extended electrocatalytic lifetime of 10 days. Notably, its stability is higher than that of non-magnetic Ni/Fe3O4/Ni and Ni/Fe3O4@PEDOT/Ni electrodes, primarily due to the support from magnetic force and the protective PEDOT layer. Moreover, the minute atomized droplets can form the H2O2 species in a moist environment, facilitating the formation of the NiO layer on the Ni surface, which plays a vital role in boosting catalytic activity. In conclusion, our magnetic electrode strategy, combined with the emergence of the NiO layer, offers valuable insights for the development of advanced HER electrodes.