TY - JOUR
T1 - Ultra-durable high-performance CoMo-MCA/Fe-NWs/NF heterostructures for industrial-grade current density seawater splitting
AU - Meena, Abhishek
AU - Jana, Atanu
AU - Shin, Giho
AU - Singh, Aditya Narayan
AU - Jang, Jae Won
AU - Im, Hyun sik
AU - Cho, Sangeun
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/10/7
Y1 - 2024/10/7
N2 - Extensive efforts are being dedicated to developing high-performance electrocatalysts for water splitting to achieve efficient and stable hydrogen production, especially under high current densities. In this study, we synthesised a CoMo microcolumn arrays (MCA)/Fe-nanowires (NWs)/nickel foam (NF) catalyst through a simple yet effective combination of hydrothermal and solution-based methods. This catalyst exhibits remarkable performance during the oxygen evolution reaction (OER), achieving a low overpotential of 425 mV at a current density of 2000 mA cm−2 and maintaining stability for 200 h at a current density of 1000 mA cm−2 in 1 M KOH. In natural alkaline seawater, the catalyst demonstrates an overpotential of 464 mV at a current density of 1000 mA cm−2, with stability extending to 250 h at a current density of 500 mA cm−2. These overpotentials are lower than that required for hypochlorite production (>490 mV). Furthermore, during alkaline full seawater splitting, the synthesised catalyst delivers a cell voltage of 1.861 V at a current density of 1000 mA cm−2, sustaining stability for 100 h at a current density of 500 mA cm−2. The heterointerfaces in the CoMo-MCA/Fe-NWs/NF structure optimise the electronic configuration, enhancing OER activity. The MCA structure and Fe2O3 NWs increase the electrochemically active surface area, providing numerous active sites and ensuring long-term durability under harsh conditions. This study suggests a promising approach for industrial-scale seawater electrolysis by engineering effective heterostructures and interfacial active sites.
AB - Extensive efforts are being dedicated to developing high-performance electrocatalysts for water splitting to achieve efficient and stable hydrogen production, especially under high current densities. In this study, we synthesised a CoMo microcolumn arrays (MCA)/Fe-nanowires (NWs)/nickel foam (NF) catalyst through a simple yet effective combination of hydrothermal and solution-based methods. This catalyst exhibits remarkable performance during the oxygen evolution reaction (OER), achieving a low overpotential of 425 mV at a current density of 2000 mA cm−2 and maintaining stability for 200 h at a current density of 1000 mA cm−2 in 1 M KOH. In natural alkaline seawater, the catalyst demonstrates an overpotential of 464 mV at a current density of 1000 mA cm−2, with stability extending to 250 h at a current density of 500 mA cm−2. These overpotentials are lower than that required for hypochlorite production (>490 mV). Furthermore, during alkaline full seawater splitting, the synthesised catalyst delivers a cell voltage of 1.861 V at a current density of 1000 mA cm−2, sustaining stability for 100 h at a current density of 500 mA cm−2. The heterointerfaces in the CoMo-MCA/Fe-NWs/NF structure optimise the electronic configuration, enhancing OER activity. The MCA structure and Fe2O3 NWs increase the electrochemically active surface area, providing numerous active sites and ensuring long-term durability under harsh conditions. This study suggests a promising approach for industrial-scale seawater electrolysis by engineering effective heterostructures and interfacial active sites.
UR - http://www.scopus.com/inward/record.url?scp=85206493706&partnerID=8YFLogxK
U2 - 10.1039/d4ta05175k
DO - 10.1039/d4ta05175k
M3 - Article
AN - SCOPUS:85206493706
SN - 2050-7488
VL - 12
SP - 30022
EP - 30031
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 43
ER -