TY - JOUR
T1 - Controlled electrochemical synthesis of bimetallic cobalt–manganese borate (CoMnBi) thin layer for enhanced clean oxygen generation reaction
T2 - Experimental and theoretical investigation
AU - Irfan, Ahamad
AU - Pirzada, Bilal Masood
AU - Talib, Shamraiz Hussain
AU - Mohamed, Sharmarke
AU - Qurashi, Ahsanulhaq
N1 - Publisher Copyright:
© 2025
PY - 2025/3/14
Y1 - 2025/3/14
N2 - There is a pressing need to develop facile synthesis methodologies and efficient earth-abundant electrocatalysts for accelerating oxygen evolution reaction (OER) that facilitates various purposes ranging from efficient green hydrogen to clean oxygen generation. In this work, a facile electrochemical deposition method was employed to synthesize bimetallic cobalt-manganese borate (x%-Co-Mn-Bi) electrocatalysts on fluorine-doped tin oxide (FTO) substrate. The bimetallic borate electrocatalysts were characterized as synthesized using XRD, SEM, EDS, and XPS studies. The electrochemical performance for OER was demonstrated using a 3-electrode electrochemical cell set-up. Due to metal-metal synergistic effects and other supporting factors, the 30%-Co-Mn-Bi exhibited the lowest overpotential among the un-annealed samples, followed by 40%-Co-Mn-Bi. However, when the samples were annealed at different temperatures, 40%-Co-Mn-Bi annealed at 200 °C showed the best overall OER performance with the least Tafel slope of 72.5 mV/dec, lower charge transfer resistance, a high electrochemical surface area, excellent turnover frequency, moderate faradaic efficiency in addition to convincing long-term stability for OER application. The results were further validated using theoretical Density Functional Theory (DFT) treatment which inferred that 30%-Co-Mn-Bi exhibits the lowest overpotential for oxygen generation reaction. This work provides a concrete and comprehensive strategy for the controlled synthesis of varying stoichiometric thin-layer bimetallic borates for efficient oxygen production with reduced usage of expensive cobalt.
AB - There is a pressing need to develop facile synthesis methodologies and efficient earth-abundant electrocatalysts for accelerating oxygen evolution reaction (OER) that facilitates various purposes ranging from efficient green hydrogen to clean oxygen generation. In this work, a facile electrochemical deposition method was employed to synthesize bimetallic cobalt-manganese borate (x%-Co-Mn-Bi) electrocatalysts on fluorine-doped tin oxide (FTO) substrate. The bimetallic borate electrocatalysts were characterized as synthesized using XRD, SEM, EDS, and XPS studies. The electrochemical performance for OER was demonstrated using a 3-electrode electrochemical cell set-up. Due to metal-metal synergistic effects and other supporting factors, the 30%-Co-Mn-Bi exhibited the lowest overpotential among the un-annealed samples, followed by 40%-Co-Mn-Bi. However, when the samples were annealed at different temperatures, 40%-Co-Mn-Bi annealed at 200 °C showed the best overall OER performance with the least Tafel slope of 72.5 mV/dec, lower charge transfer resistance, a high electrochemical surface area, excellent turnover frequency, moderate faradaic efficiency in addition to convincing long-term stability for OER application. The results were further validated using theoretical Density Functional Theory (DFT) treatment which inferred that 30%-Co-Mn-Bi exhibits the lowest overpotential for oxygen generation reaction. This work provides a concrete and comprehensive strategy for the controlled synthesis of varying stoichiometric thin-layer bimetallic borates for efficient oxygen production with reduced usage of expensive cobalt.
KW - Bimetallic borates
KW - Cobalt borate
KW - Electrodeposition
KW - Manganese borate
KW - Oxygen evolution reaction
KW - Thin film
UR - https://www.scopus.com/pages/publications/85217542293
U2 - 10.1016/j.ijhydene.2025.02.022
DO - 10.1016/j.ijhydene.2025.02.022
M3 - Article
AN - SCOPUS:85217542293
SN - 0360-3199
VL - 109
SP - 636
EP - 647
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -