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Binder-Free Spinel Co2CuO4 Nanosheet Electrodes with Cu-Driven Kinetic Enhancement for Alkaline OER Applicationsopen access

Authors
Ahmed, Abu Talha AqueelMujtaba, Momin M.Ansari, Abu SaadCho, Sangeun
Issue Date
Jan-2026
Publisher
MDPI
Keywords
electrodeposition; Co2CuO4; nanosheets; Co3O4; OER; prolonged electrolysis
Citation
Materials, v.19, no.2, pp 1 - 17
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
Materials
Volume
19
Number
2
Start Page
1
End Page
17
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/63660
DOI
10.3390/ma19020301
ISSN
1996-1944
1996-1944
Abstract
Developing electrocatalysts that are efficient and durable for the oxygen evolution reaction (OER) is essential for improving the energy efficiency of alkaline water splitting. Spinel-type transition-metal oxides have emerged as promising non-noble alternatives; however, their catalytic performance is often limited by sluggish charge transport and insufficient utilization of active sites. Herein, we present a systematic comparative study of electrodeposited Co3O4 (CO-300) and Cu-substituted Co2CuO4 (CCO-300) nanosheet films directly grown on Ni foam. Structural, morphological, and spectroscopic analyses reveal that Cu2+ integration into Co-oxide spinel lattice modifies the local electronic environment and produces a more open and interconnected nanosheet architecture, thereby enhancing conductivity and increasing the density of accessible redox-active sites. As a result, the optimized CCO-300 exhibits superior catalytic performance at higher current densities, along with a smaller Tafel slope (44 mV dec(-1)), a larger electrochemically active surface area (ECSA), and reduced charge-transfer resistance compared to CCO-300, indicating accelerated reaction kinetics and improved electron-ion transport. Furthermore, the multistep chronopotentiometry measurements and long-term stability tests over 100 h at current densities of 10 and 250 mA cm(-2) highlight the excellent operational stability of the CCO-300 catalyst.
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