TY - JOUR
T1 - Ce-doped NiCoP/ Co3O4 composite Nanostructures on Ni foam and their enhanced performance for water and urea electrolysis
AU - Liu, Zhe
AU - Lee, Soyeon
AU - Zhou, Tao
AU - Yang, Jiwoong
AU - Yu, Taekyung
N1 - Publisher Copyright:
© 2025 Elsevier Inc.
PY - 2025/8/15
Y1 - 2025/8/15
N2 - Producing hydrogen through freshwater or urea-containing wastewater electrolysis using renewable electricity requires multifunctional catalysts made from nonprecious metals. In the current study, we disclose the rational fabrication of oxide/phosphide heterostructure nanorods with rare earth metal doping on nickel foam (NF), denoted Ce-NiCoP/Co3O4/NF, via partial phosphorization. Benefiting from intrinsic interface formation and doping effects, the interaction between the coupling components facilitates electron transfer, optimizing the electronic configuration of the Ce-NiCoP/Co3O4/NF catalyst. Ce-NiCoP/Co3O4/NF exhibited a competitive potential of − 0.151 V for hydrogen evolution reaction, 1.50 V for oxygen evolution reaction (OER), and 1.33 V (versus reversible hydrogen electrode) toward urea oxidation reactions (UOR) at 100 mA cm−2. In situ Fourier-transform infrared combined with electrochemical analysis detects *OOH and *O2 − intermediates in OER, as well as CO3 2− and CNO− ions, alongside the N–H vibration in UOR, providing deeper insight into the OER and UOR mechanisms on the Ce-NiCoP/Co3O4/NF. More importantly, the catalyst exhibited an activity of 20 mA cm−2 requiring voltages as low as 1.52 V for unassisted water splitting and 1.27 V for urea-assisted electrolysis.
AB - Producing hydrogen through freshwater or urea-containing wastewater electrolysis using renewable electricity requires multifunctional catalysts made from nonprecious metals. In the current study, we disclose the rational fabrication of oxide/phosphide heterostructure nanorods with rare earth metal doping on nickel foam (NF), denoted Ce-NiCoP/Co3O4/NF, via partial phosphorization. Benefiting from intrinsic interface formation and doping effects, the interaction between the coupling components facilitates electron transfer, optimizing the electronic configuration of the Ce-NiCoP/Co3O4/NF catalyst. Ce-NiCoP/Co3O4/NF exhibited a competitive potential of − 0.151 V for hydrogen evolution reaction, 1.50 V for oxygen evolution reaction (OER), and 1.33 V (versus reversible hydrogen electrode) toward urea oxidation reactions (UOR) at 100 mA cm−2. In situ Fourier-transform infrared combined with electrochemical analysis detects *OOH and *O2 − intermediates in OER, as well as CO3 2− and CNO− ions, alongside the N–H vibration in UOR, providing deeper insight into the OER and UOR mechanisms on the Ce-NiCoP/Co3O4/NF. More importantly, the catalyst exhibited an activity of 20 mA cm−2 requiring voltages as low as 1.52 V for unassisted water splitting and 1.27 V for urea-assisted electrolysis.
KW - Self-supported material
KW - Trifunctional electrocatalyst
KW - Water splitting
UR - https://www.scopus.com/pages/publications/105002218164
U2 - 10.1016/j.jcis.2025.137542
DO - 10.1016/j.jcis.2025.137542
M3 - Article
C2 - 40220637
AN - SCOPUS:105002218164
SN - 0021-9797
VL - 692
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
M1 - 137542
ER -