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LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution

Metal–organic frameworks (MOFs) have emerged as alternative OER catalysts due to their easy regulation, such as in situ self-reconstruction from MOFs to metal hydroxides through alkaline hydrolysis. Herein, we demonstrate a facile strategy for the in situ transformation of FeCo layered double hydrox...

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Autores principales: Tang, Lin, Cai, Minjuan, Zhang, Maosheng, Chen, Xi, Cai, Zhixiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443477/
https://www.ncbi.nlm.nih.gov/pubmed/36199872
http://dx.doi.org/10.1039/d2ra04871j
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author Tang, Lin
Cai, Minjuan
Zhang, Maosheng
Chen, Xi
Cai, Zhixiong
author_facet Tang, Lin
Cai, Minjuan
Zhang, Maosheng
Chen, Xi
Cai, Zhixiong
author_sort Tang, Lin
collection PubMed
description Metal–organic frameworks (MOFs) have emerged as alternative OER catalysts due to their easy regulation, such as in situ self-reconstruction from MOFs to metal hydroxides through alkaline hydrolysis. Herein, we demonstrate a facile strategy for the in situ transformation of FeCo layered double hydroxide (FeCo-LDH) nanosheets into 1D spindle-shaped FeCo-MOFs for efficient OER. An optimized electrode of FeCo-MOF on a nickel foam (NF) was achieved by adjusting the addition of organic ligands and the reaction time in the hydrothermal reaction. Based on the unique 1D nanostructure and the cation regulation, the obtained FeCo-MOF exhibits a good catalytic performance toward the OER with a low overpotential of 475 mV at 100 mA cm(−2), a small Tafel slope of 121.8 mV dec(−1), and high long-term durability. This study provides a facile strategy for preparing bimetal-MOFs as catalysts for efficient OER.
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spelling pubmed-94434772022-10-04 LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution Tang, Lin Cai, Minjuan Zhang, Maosheng Chen, Xi Cai, Zhixiong RSC Adv Chemistry Metal–organic frameworks (MOFs) have emerged as alternative OER catalysts due to their easy regulation, such as in situ self-reconstruction from MOFs to metal hydroxides through alkaline hydrolysis. Herein, we demonstrate a facile strategy for the in situ transformation of FeCo layered double hydroxide (FeCo-LDH) nanosheets into 1D spindle-shaped FeCo-MOFs for efficient OER. An optimized electrode of FeCo-MOF on a nickel foam (NF) was achieved by adjusting the addition of organic ligands and the reaction time in the hydrothermal reaction. Based on the unique 1D nanostructure and the cation regulation, the obtained FeCo-MOF exhibits a good catalytic performance toward the OER with a low overpotential of 475 mV at 100 mA cm(−2), a small Tafel slope of 121.8 mV dec(−1), and high long-term durability. This study provides a facile strategy for preparing bimetal-MOFs as catalysts for efficient OER. The Royal Society of Chemistry 2022-09-05 /pmc/articles/PMC9443477/ /pubmed/36199872 http://dx.doi.org/10.1039/d2ra04871j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tang, Lin
Cai, Minjuan
Zhang, Maosheng
Chen, Xi
Cai, Zhixiong
LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution
title LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution
title_full LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution
title_fullStr LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution
title_full_unstemmed LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution
title_short LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution
title_sort ldh-assisted growth of feco bimetal-mof nanorods for electrocatalytic oxygen evolution
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443477/
https://www.ncbi.nlm.nih.gov/pubmed/36199872
http://dx.doi.org/10.1039/d2ra04871j
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