CTAB‐Assisted Hydrothermal Synthesis of CoFeMo Layered Double Hydroxides for Efficient Oxygen Evolution Reactions

The sluggish kinetics of the oxygen evolution reaction (OER), one of the half-reactions in water electrolysis, severely constrains the large-scale implementation of this technology. Therefore, identifying electrocatalysts with superior OER performance is of critical importance. In this study, a CTAB-assisted hydrothermal method was employed to synthesize CoFeMo layered double hydroxide (LDH) nanosheets on nickel foam (NF) to achieve enhanced OER activity. The incorporation of Mo resulted in an increased number of active sites and improved electrical conductivity, yielding overpotentials of 164 and 265 mV at 10 and 50 mA cm<sup>-2</sup>, respectively surpassing the performance of both CoFe LDH/NF and RuO₂/NF, as well as most previously reported OER catalysts. The exceptional activity was attributed to the high valence state of Mo, which stabilizes neighboring metals through electronic structure modulation. In addition, the presence of the cationic surfactant CTAB during the hydrothermal process effectively suppressed metal agglomeration and regulated the morphology. Overall, this work demonstrates that CoFeMo LDH/NF synthesized via CTAB-assisted hydrothermal methods serves as a highly effective electrocatalyst for oxygen evolution reactions.

Authors

Institutions

Publication Details

Journal
Chemistry - An Asian Journal
Published
2025-02-13
DOI
https://doi.org/10.1002/asia.202401688
Citations
2
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.73

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

CTAB‐Assisted Hydrothermal Synthesis of CoFeMo Layered Double Hydroxides for Efficient Oxygen Evolution Reactions

Kun Liang, Jiantai Ma, Hao‐Li Zhang, Miao Li et al.
2 citations
Chemistry - An Asian Journal
Electrocatalysts for Energy Conversion
0.73
article

CTAB‐Assisted Hydrothermal Synthesis of CoFeMo Layered Double Hydroxides for Efficient Oxygen Evolution Reactions

Kun Liang, Jiantai Ma, Hao‐Li Zhang, Miao Li, Ming Chen, Jing Wang, Jinli Duan, S.Y. Ma
article en
2 citations

Abstract

The sluggish kinetics of the oxygen evolution reaction (OER), one of the half-reactions in water electrolysis, severely constrains the large-scale implementation of this technology. Therefore, identifying electrocatalysts with superior OER performance is of critical importance. In this study, a CTAB-assisted hydrothermal method was employed to synthesize CoFeMo layered double hydroxide (LDH) nanosheets on nickel foam (NF) to achieve enhanced OER activity. The incorporation of Mo resulted in an increased number of active sites and improved electrical conductivity, yielding overpotentials of 164 and 265 mV at 10 and 50 mA cm<sup>-2</sup>, respectively surpassing the performance of both CoFe LDH/NF and RuO₂/NF, as well as most previously reported OER catalysts. The exceptional activity was attributed to the high valence state of Mo, which stabilizes neighboring metals through electronic structure modulation. In addition, the presence of the cationic surfactant CTAB during the hydrothermal process effectively suppressed metal agglomeration and regulated the morphology. Overall, this work demonstrates that CoFeMo LDH/NF synthesized via CTAB-assisted hydrothermal methods serves as a highly effective electrocatalyst for oxygen evolution reactions.

Chemistry - An Asian JournalVol. 20(10)
Lanzhou University (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Clean water and sanitation
Openalex Percentile: Top 33%
Electrocatalysts for Energy Conversion
0.73
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.