TY - JOUR
T1 - Carbon nanotube/metal organic framework hybrid scaffolds for scalable and self-structured OER catalyst coating
T2 - From rheology study to MEA fabrication
AU - Lee, Suhyeon
AU - Ji, Yunseong
AU - Doo, Gisu
AU - Kim, Min Joong
AU - Shin, Jooyoung
AU - Kim, Chansol
AU - Han, Man Ho
AU - Lee, Woong Hee
AU - Lee, Jong Hyup
AU - Kwak, Yeonji
AU - Choi, Eunji
AU - Cho, Yonghwi
AU - Lee, Choong Hoo
AU - Kim, Minsu
AU - Park, Jung Tae
AU - Kim, Dae Woo
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/4/1
Y1 - 2025/4/1
N2 - We developed a scalable binder-free composite electrode layer fabrication method by integrating Fe-Ni-based MIL-101 MOF catalysts for the oxygen evolution reaction (OER) with carbon nanotube (CNT) scaffolds. This synergy significantly enhanced active site exposure, as the MOF uniformly dispersed across the CNT surface, forming a 3D electroconductive structure. In particular, the MOFs are further transformed into the hybrid structure of metal hydroxide and organic compounds during OER conditions, leading to an enhanced and stable catalytic layer. The resulting electrode exhibited improved catalytic performance, with overpotentials of 263 mV at 10 mA/cm2 and 355 mV at 100 mA/cm2 in half-cell tests. In an alkaline exchange membrane water electrolyzer (AEMWE), the electrode achieved a voltage of 1.8 V at 1 A/cm2, with an overpotential 0.69 V lower than that of the conventional IrOx/Nafion_CC electrode at a loading of 0.2 mg cm−2. Our method effectively overcomes the scalability challenges associated with traditional catalyst growth strategies and demonstrates that MOF materials can function as electrocatalysts without further treatment.
AB - We developed a scalable binder-free composite electrode layer fabrication method by integrating Fe-Ni-based MIL-101 MOF catalysts for the oxygen evolution reaction (OER) with carbon nanotube (CNT) scaffolds. This synergy significantly enhanced active site exposure, as the MOF uniformly dispersed across the CNT surface, forming a 3D electroconductive structure. In particular, the MOFs are further transformed into the hybrid structure of metal hydroxide and organic compounds during OER conditions, leading to an enhanced and stable catalytic layer. The resulting electrode exhibited improved catalytic performance, with overpotentials of 263 mV at 10 mA/cm2 and 355 mV at 100 mA/cm2 in half-cell tests. In an alkaline exchange membrane water electrolyzer (AEMWE), the electrode achieved a voltage of 1.8 V at 1 A/cm2, with an overpotential 0.69 V lower than that of the conventional IrOx/Nafion_CC electrode at a loading of 0.2 mg cm−2. Our method effectively overcomes the scalability challenges associated with traditional catalyst growth strategies and demonstrates that MOF materials can function as electrocatalysts without further treatment.
KW - Carbon nanotube
KW - Large-area catalyst coating
KW - Membrane electrode assembly
KW - Metal-organic framework
KW - Oxygen evolution reaction
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U2 - 10.1016/j.cej.2025.161533
DO - 10.1016/j.cej.2025.161533
M3 - Article
AN - SCOPUS:86000754355
SN - 1385-8947
VL - 509
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 161533
ER -