A non-noble metal Li, Mn co-doped Ni3S2 electrocatalyst for glycerol oxidation synergistic coupling to promote the hydrogen evolution reaction

• Published in: New journal of chemistry 2024-09, Vol.48 (35), p.15470-15482
• Main Authors: Wang, Qingtao, Zhou, Xiaoling, Jin, Hanbin, Guo, Lulu, Wu, Yanxia, Ren, Shufang
• Format: Article
• Language: English
• Subjects: Anodizing; Electrocatalysts; Electrolysis; Electron transfer; Energy consumption; Glycerol; Hydrogen evolution reactions; Hydrogen production; Metal foams; Nickel sulfide; Noble metals; Organic compounds; Oxidation
• ISSN: 1144-0546; 1369-9261
• DOI: 10.1039/d4nj03067b

As one of the effective methods for hydrogen production, water electrolysis has been widely studied. However, the high overpotential challenge faced by the anode and the limitation of the electron transfer rate in this process significantly inhibit the efficiency of hydrogen production, which has become the main obstacle to overcome in the current research. The use of thermodynamically more favorable organic compounds to oxidize at the anode instead of traditional water oxidation (OER) is an effective strategy to optimize the process of electrolytic hydrogen production. In this paper, Ni3S2 catalysts co-doped with non-noble metals Li and Mn were prepared on nickel foam and used for the glycerol oxidation reaction (GOR) coupled with the hydrogen evolution reaction (HER). In alkaline solution, Li, Mn–Ni3S2@NF exhibits good GOR and HER performance. Specifically, overpotentials of 1.58 V vs. RHE and 0.54 V vs. RHE are required to reach a current density of 200 mA cm−2, respectively, and the catalytic performance of the material remains good after a long-term test. Li, Mn–Ni3S2@NF as a bifunctional catalytic material oxidizes glycerol to formate, and its faradaic efficiency (FE) is as high as 91%, and the volume of hydrogen production is close to the theoretical value. In addition, the replacement of the OER by the GOR can reduce the energy consumption by about 17.44%.