Elucidating the performance of hexamethylene tetra-amine interlinked bimetallic NiCo-MOF for efficient electrochemical hydrogen and oxygen evolution
Bimetallic metal-organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nano...
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Published in: | RSC advances Vol. 14; no. 2; pp. 13837 - 13849 |
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25-04-2024
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Abstract | Bimetallic metal-organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nanostructure as a potent bifunctional electrocatalyst with superior performance for overall water splitting in alkaline environments. The structural, morphological, and electrochemical properties of the as-synthesized bifunctional catalyst were examined thoroughly before analyzing its behavior towards electrochemical water splitting. The HMT-based NiCo-MOF demonstrated small overpotential values of 274 mV and 330 mV in reaching a maximum current density of 30 mA cm
−2
for hydrogen and oxygen evolution mechanisms, respectively. The Tafel parameter also showed favorable HER/OER reaction kinetics, with slopes of 78 mV dec
−1
and 86 mV dec
−1
determined during the electrochemical evaluation. Remarkably, the NiCo-HMT electrode exhibited a double-layer capacitance of 4 mF cm
2
for hydrogen evolution and 23 mF cm
−2
for oxygen evolution, while maintaining remarkable stability even after continuous operation for 20 hours. This research offers a valuable blueprint for implementing a cost-effective and durable MOF-based bifunctional catalytic system that has proven to be effective for complete water splitting. Decomposition of water under higher current densities is crucial for effective long-term generation and commercial consumption of hydrogen.
This study investigates the electrocatalytic water splitting capabilities of hexamethylene tetra-amine-linked NiCo-MOF, synthesized
via
hydrothermal approach. It reveals low overpotentials of 274 mV and 330 mV with Tafel slopes of 78 mV dec
−1
and 86 mV dec
−1
towards HER and OER respectively. |
---|---|
AbstractList | Bimetallic metal-organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nanostructure as a potent bifunctional electrocatalyst with superior performance for overall water splitting in alkaline environments. The structural, morphological, and electrochemical properties of the as-synthesized bifunctional catalyst were examined thoroughly before analyzing its behavior towards electrochemical water splitting. The HMT-based NiCo-MOF demonstrated small overpotential values of 274 mV and 330 mV in reaching a maximum current density of 30 mA cm
−2
for hydrogen and oxygen evolution mechanisms, respectively. The Tafel parameter also showed favorable HER/OER reaction kinetics, with slopes of 78 mV dec
−1
and 86 mV dec
−1
determined during the electrochemical evaluation. Remarkably, the NiCo-HMT electrode exhibited a double-layer capacitance of 4 mF cm
2
for hydrogen evolution and 23 mF cm
−2
for oxygen evolution, while maintaining remarkable stability even after continuous operation for 20 hours. This research offers a valuable blueprint for implementing a cost-effective and durable MOF-based bifunctional catalytic system that has proven to be effective for complete water splitting. Decomposition of water under higher current densities is crucial for effective long-term generation and commercial consumption of hydrogen.
This study investigates the electrocatalytic water splitting capabilities of hexamethylene tetra-amine-linked NiCo-MOF, synthesized
via
hydrothermal approach. It reveals low overpotentials of 274 mV and 330 mV with Tafel slopes of 78 mV dec
−1
and 86 mV dec
−1
towards HER and OER respectively. Bimetallic metal-organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nanostructure as a potent bifunctional electrocatalyst with superior performance for overall water splitting in alkaline environments. The structural, morphological, and electrochemical properties of the as-synthesized bifunctional catalyst were examined thoroughly before analyzing its behavior towards electrochemical water splitting. The HMT-based NiCo-MOF demonstrated small overpotential values of 274 mV and 330 mV in reaching a maximum current density of 30 mA cm for hydrogen and oxygen evolution mechanisms, respectively. The Tafel parameter also showed favorable HER/OER reaction kinetics, with slopes of 78 mV dec and 86 mV dec determined during the electrochemical evaluation. Remarkably, the NiCo-HMT electrode exhibited a double-layer capacitance of 4 mF cm for hydrogen evolution and 23 mF cm for oxygen evolution, while maintaining remarkable stability even after continuous operation for 20 hours. This research offers a valuable blueprint for implementing a cost-effective and durable MOF-based bifunctional catalytic system that has proven to be effective for complete water splitting. Decomposition of water under higher current densities is crucial for effective long-term generation and commercial consumption of hydrogen. Bimetallic metal–organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nanostructure as a potent bifunctional electrocatalyst with superior performance for overall water splitting in alkaline environments. The structural, morphological, and electrochemical properties of the as-synthesized bifunctional catalyst were examined thoroughly before analyzing its behavior towards electrochemical water splitting. The HMT-based NiCo-MOF demonstrated small overpotential values of 274 mV and 330 mV in reaching a maximum current density of 30 mA cm−2 for hydrogen and oxygen evolution mechanisms, respectively. The Tafel parameter also showed favorable HER/OER reaction kinetics, with slopes of 78 mV dec−1 and 86 mV dec−1 determined during the electrochemical evaluation. Remarkably, the NiCo-HMT electrode exhibited a double-layer capacitance of 4 mF cm−2 for hydrogen evolution and 23 mF cm−2 for oxygen evolution, while maintaining remarkable stability even after continuous operation for 20 hours. This research offers a valuable blueprint for implementing a cost-effective and durable MOF-based bifunctional catalytic system that has proven to be effective for complete water splitting. Decomposition of water under higher current densities is crucial for effective long-term generation and commercial consumption of hydrogen. Bimetallic metal-organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nanostructure as a potent bifunctional electrocatalyst with superior performance for overall water splitting in alkaline environments. The structural, morphological, and electrochemical properties of the as-synthesized bifunctional catalyst were examined thoroughly before analyzing its behavior towards electrochemical water splitting. The HMT-based NiCo-MOF demonstrated small overpotential values of 274 mV and 330 mV in reaching a maximum current density of 30 mA cm-2 for hydrogen and oxygen evolution mechanisms, respectively. The Tafel parameter also showed favorable HER/OER reaction kinetics, with slopes of 78 mV dec-1 and 86 mV dec-1 determined during the electrochemical evaluation. Remarkably, the NiCo-HMT electrode exhibited a double-layer capacitance of 4 mF cm-2 for hydrogen evolution and 23 mF cm-2 for oxygen evolution, while maintaining remarkable stability even after continuous operation for 20 hours. This research offers a valuable blueprint for implementing a cost-effective and durable MOF-based bifunctional catalytic system that has proven to be effective for complete water splitting. Decomposition of water under higher current densities is crucial for effective long-term generation and commercial consumption of hydrogen. Bimetallic metal–organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of increased numbers of pores. For the inaugural time, we examine the effectiveness of a hexamethylene tetra-amine (HMT)-induced 3D NiCo-MOF-based nanostructure as a potent bifunctional electrocatalyst with superior performance for overall water splitting in alkaline environments. The structural, morphological, and electrochemical properties of the as-synthesized bifunctional catalyst were examined thoroughly before analyzing its behavior towards electrochemical water splitting. The HMT-based NiCo-MOF demonstrated small overpotential values of 274 mV and 330 mV in reaching a maximum current density of 30 mA cm −2 for hydrogen and oxygen evolution mechanisms, respectively. The Tafel parameter also showed favorable HER/OER reaction kinetics, with slopes of 78 mV dec −1 and 86 mV dec −1 determined during the electrochemical evaluation. Remarkably, the NiCo-HMT electrode exhibited a double-layer capacitance of 4 mF cm −2 for hydrogen evolution and 23 mF cm −2 for oxygen evolution, while maintaining remarkable stability even after continuous operation for 20 hours. This research offers a valuable blueprint for implementing a cost-effective and durable MOF-based bifunctional catalytic system that has proven to be effective for complete water splitting. Decomposition of water under higher current densities is crucial for effective long-term generation and commercial consumption of hydrogen. |
Author | Abdul Karim, Muhammad Ramzan Marwat, Mohsin Ali Zahid, Rida Khan, Fahd Sikandar |
AuthorAffiliation | Faculty of Engineering Sciences Faculty of Materials and Chemical Engineering Ghulam Ishaq Khan Institute of Engineering Sciences and Technology |
AuthorAffiliation_xml | – name: Ghulam Ishaq Khan Institute of Engineering Sciences and Technology – name: Faculty of Materials and Chemical Engineering – name: Faculty of Engineering Sciences |
Author_xml | – sequence: 1 givenname: Rida surname: Zahid fullname: Zahid, Rida – sequence: 2 givenname: Muhammad Ramzan surname: Abdul Karim fullname: Abdul Karim, Muhammad Ramzan – sequence: 3 givenname: Fahd Sikandar surname: Khan fullname: Khan, Fahd Sikandar – sequence: 4 givenname: Mohsin Ali surname: Marwat fullname: Marwat, Mohsin Ali |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38681836$$D View this record in MEDLINE/PubMed |
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Snippet | Bimetallic metal-organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of... Bimetallic metal–organic frameworks (MOFs) play a significant role in the electrocatalysis of water due to their large surface area and availability of... |
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SubjectTerms | Bimetals Chemical synthesis Current density Electrocatalysts Electrochemical analysis Hydrogen Hydrogen evolution Intermetallic compounds Metal-organic frameworks Oxygen evolution reactions Reaction kinetics Tafel slopes Water splitting |
Title | Elucidating the performance of hexamethylene tetra-amine interlinked bimetallic NiCo-MOF for efficient electrochemical hydrogen and oxygen evolution |
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