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Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction

Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal–organic f...

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Autores principales: You, Sheng-Mu, El Rouby, Waleed M. A., Thamilselvan, Annadurai, Tsai, Cheng-Kuo, Darmanto, Win, Doong, Ruey-An, Millet, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559871/
https://www.ncbi.nlm.nih.gov/pubmed/32867259
http://dx.doi.org/10.3390/nano10091688
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author You, Sheng-Mu
El Rouby, Waleed M. A.
Thamilselvan, Annadurai
Tsai, Cheng-Kuo
Darmanto, Win
Doong, Ruey-An
Millet, Pierre
author_facet You, Sheng-Mu
El Rouby, Waleed M. A.
Thamilselvan, Annadurai
Tsai, Cheng-Kuo
Darmanto, Win
Doong, Ruey-An
Millet, Pierre
author_sort You, Sheng-Mu
collection PubMed
description Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal–organic framework (MOF)-derived bimetallic electrocatalysis with its superior performance has wide application prospects in OER and PEC applications. Herein, we have fabricated a nickel and iron bimetallic organic framework (FeNi-MOF) deposited on top of anodized TiO(2) nanotube arrays (TNTA) for PEC and OER applications. The FeNi-MOF/TNTA was incorporated through the electrochemical deposition of Ni(2+) and Fe(3+) onto the surface of TNTA and then connected with organic ligands by the hydrothermal transformation. Therefore, FeNi-MOF/TNTA demonstrates abundant photoelectrocatalytic active sites that can enhance the photocurrent up to 1.91 mA/cm(2) under 100 mW/cm(2) and a negligible loss in activity after 180 min of photoreaction. The FeNi-MOF-doped photoanode shows predominant photoelectrochemical performance due to the boosted excellent light-harvesting ability, rapid photoresponse, and stimulated interfacial energy of charge separation under the UV-visible light irradiation conditions. The results of this study give deep insight into MOF-derived bimetallic nanomaterial synthesis for photoelectrochemical OER and provide guidance on future electrocatalysis design.
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spelling pubmed-75598712020-10-22 Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction You, Sheng-Mu El Rouby, Waleed M. A. Thamilselvan, Annadurai Tsai, Cheng-Kuo Darmanto, Win Doong, Ruey-An Millet, Pierre Nanomaterials (Basel) Article Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal–organic framework (MOF)-derived bimetallic electrocatalysis with its superior performance has wide application prospects in OER and PEC applications. Herein, we have fabricated a nickel and iron bimetallic organic framework (FeNi-MOF) deposited on top of anodized TiO(2) nanotube arrays (TNTA) for PEC and OER applications. The FeNi-MOF/TNTA was incorporated through the electrochemical deposition of Ni(2+) and Fe(3+) onto the surface of TNTA and then connected with organic ligands by the hydrothermal transformation. Therefore, FeNi-MOF/TNTA demonstrates abundant photoelectrocatalytic active sites that can enhance the photocurrent up to 1.91 mA/cm(2) under 100 mW/cm(2) and a negligible loss in activity after 180 min of photoreaction. The FeNi-MOF-doped photoanode shows predominant photoelectrochemical performance due to the boosted excellent light-harvesting ability, rapid photoresponse, and stimulated interfacial energy of charge separation under the UV-visible light irradiation conditions. The results of this study give deep insight into MOF-derived bimetallic nanomaterial synthesis for photoelectrochemical OER and provide guidance on future electrocatalysis design. MDPI 2020-08-27 /pmc/articles/PMC7559871/ /pubmed/32867259 http://dx.doi.org/10.3390/nano10091688 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
You, Sheng-Mu
El Rouby, Waleed M. A.
Thamilselvan, Annadurai
Tsai, Cheng-Kuo
Darmanto, Win
Doong, Ruey-An
Millet, Pierre
Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction
title Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction
title_full Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction
title_fullStr Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction
title_full_unstemmed Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction
title_short Fe/Ni Bimetallic Organic Framework Deposited on TiO(2) Nanotube Array for Enhancing Higher and Stable Photoelectrochemical Activity of Oxygen Evaluation Reaction
title_sort fe/ni bimetallic organic framework deposited on tio(2) nanotube array for enhancing higher and stable photoelectrochemical activity of oxygen evaluation reaction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559871/
https://www.ncbi.nlm.nih.gov/pubmed/32867259
http://dx.doi.org/10.3390/nano10091688
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