Design a promising electro-catalyst for oxygen reduction reaction in fuel cells based on transition metal doped in BN monolayer
The kinetic of the oxygen reduction reaction (ORR) at the cathodes of polymer-electrolyte-membrane fuel cells (PEMFCs) has been demonstrated to be slow, which is one of the pivotal issues in developing PEMFCs. Within the current piece of research, by performing first-principles calculations, we intr...
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Published in | International journal of hydrogen energy Vol. 50; pp. 161 - 168 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
02.01.2024
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Abstract | The kinetic of the oxygen reduction reaction (ORR) at the cathodes of polymer-electrolyte-membrane fuel cells (PEMFCs) has been demonstrated to be slow, which is one of the pivotal issues in developing PEMFCs. Within the current piece of research, by performing first-principles calculations, we introduce a Co-doped vacancy BN nanosheet (Co-HBN) as an efficacious noble metal-free electro-catalyst for the ORR process (ORRP) in fuel cells. The results demonstrate a rise in the energies of adsorption (or adhesion) onto the Co–N active site of these electrocatalysts in the order of O < OH < OOH < O2 < H2O2 < H2O on this electrocatalyst and there is a consistent change in the adsorption energies (Eads)for all oxygen-containing intermediates (OCIs). Based on the small and large thermodynamic driving force for the generation of H2O2 and for reducing OOH into O∗ (or to 2OH∗), respectively, the four-electron route was more favorable in comparison with the 2e− route. Furthermore, with the largest value of ΔG for Co-HBN electrocatalyst, the final reduction step (OH∗ + H+ + e− → H2O + ∗) has been regarded as the rate-limiting step. The d-band center of Co was considerably distant from the Fermi level. The greater gap between the frontier orbitals suggested that the electrocatalyst is not conducive to the adsorption of OCIs, which shows that the onset potential is larger and ORR is high.
•The catalytic activity of a series of Co-doped v-BN has been theoretically explored in the ORR.•O2 molecule can be directly dissociated on the Co-doped v-BN with 4e pathway.•It is reacting more favorable for the ER mechanism of OH∗ to convert into H2O.•The ORR reaction was found to be thermodynamically favorable in the Co-doped v-BN. |
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AbstractList | The kinetic of the oxygen reduction reaction (ORR) at the cathodes of polymer-electrolyte-membrane fuel cells (PEMFCs) has been demonstrated to be slow, which is one of the pivotal issues in developing PEMFCs. Within the current piece of research, by performing first-principles calculations, we introduce a Co-doped vacancy BN nanosheet (Co-HBN) as an efficacious noble metal-free electro-catalyst for the ORR process (ORRP) in fuel cells. The results demonstrate a rise in the energies of adsorption (or adhesion) onto the Co–N active site of these electrocatalysts in the order of O < OH < OOH < O2 < H2O2 < H2O on this electrocatalyst and there is a consistent change in the adsorption energies (Eads)for all oxygen-containing intermediates (OCIs). Based on the small and large thermodynamic driving force for the generation of H2O2 and for reducing OOH into O∗ (or to 2OH∗), respectively, the four-electron route was more favorable in comparison with the 2e− route. Furthermore, with the largest value of ΔG for Co-HBN electrocatalyst, the final reduction step (OH∗ + H+ + e− → H2O + ∗) has been regarded as the rate-limiting step. The d-band center of Co was considerably distant from the Fermi level. The greater gap between the frontier orbitals suggested that the electrocatalyst is not conducive to the adsorption of OCIs, which shows that the onset potential is larger and ORR is high.
•The catalytic activity of a series of Co-doped v-BN has been theoretically explored in the ORR.•O2 molecule can be directly dissociated on the Co-doped v-BN with 4e pathway.•It is reacting more favorable for the ER mechanism of OH∗ to convert into H2O.•The ORR reaction was found to be thermodynamically favorable in the Co-doped v-BN. |
Author | Vargas-Portugal, S. Kevin Hsu, Chou-Yi Naranjo Vargas, Eugenia Mercedes Ulloa, Nestor Saeed, Shakir Mahmood Majdi, Hasan Sh Lagum, Abdelmajeed Adam Saraswat, Shelesh Krishna |
Author_xml | – sequence: 1 givenname: Chou-Yi surname: Hsu fullname: Hsu, Chou-Yi organization: Department of pharmacy, Chia Nan University of Pharmacy and Science, Tainan, Taiwan – sequence: 2 givenname: Nestor surname: Ulloa fullname: Ulloa, Nestor email: nestor.ulloa@espoch.edu.ec organization: Facultad de Ingeniería Mecánica, Escuela Superior Politécnica de Chimborazo (ESPOCH), Riobamba, 060155, Ecuador – sequence: 3 givenname: Eugenia Mercedes surname: Naranjo Vargas fullname: Naranjo Vargas, Eugenia Mercedes organization: Facultad de Ingeniería Mecánica, Escuela Superior Politécnica de Chimborazo (ESPOCH), Riobamba, 060155, Ecuador – sequence: 4 givenname: Shelesh Krishna surname: Saraswat fullname: Saraswat, Shelesh Krishna email: sheleshkrishnasaraswat@gmail.com organization: Department of Electronics and communication Engineering, GLA University, 281406, Mathura, Uttar Pradesh, India – sequence: 5 givenname: Shakir Mahmood surname: Saeed fullname: Saeed, Shakir Mahmood organization: Department of Pharmacy, Al-Noor University College, Nineveh, Iraq – sequence: 6 givenname: S. Kevin surname: Vargas-Portugal fullname: Vargas-Portugal, S. Kevin organization: Universidad Tecnológica de los Andes, Perú – sequence: 7 givenname: Hasan Sh surname: Majdi fullname: Majdi, Hasan Sh organization: Department of Chemical Engineering and Petroleum Industries, Al- Mustaqbal University, 51001, Hilla, Iraq – sequence: 8 givenname: Abdelmajeed Adam surname: Lagum fullname: Lagum, Abdelmajeed Adam organization: Department of Civil Engineering, Faculty of Engineering, Isra University, P.O. Box 22, Amman, 11622, Jordan |
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Keywords | Thermodynamic driving force Electrocatalyst Adsorption energies Oxygen reduction reaction Fuel cells |
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Snippet | The kinetic of the oxygen reduction reaction (ORR) at the cathodes of polymer-electrolyte-membrane fuel cells (PEMFCs) has been demonstrated to be slow, which... |
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SubjectTerms | Adsorption energies Electrocatalyst Fuel cells Oxygen reduction reaction Thermodynamic driving force |
Title | Design a promising electro-catalyst for oxygen reduction reaction in fuel cells based on transition metal doped in BN monolayer |
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