MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS

Graphene-based catalysts (M-N-C) have emerged as an alternative to platinum catalysts in fuel cell cathodes due to their low cost and abundant availability. Among the graphene-based catalysts under investigation, the Mangan-Nikel dual-atom catalyst (DAC) shows potential as an alternative due to its...

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Main Author: Helmi, Faizal
Format: Theses
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/86798
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:86798
spelling id-itb.:867982024-12-23T12:22:58ZMECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS Helmi, Faizal Indonesia Theses Dual-Atom Catalyst (DAC), MnNiN6, DFT, ORR, fuel cell. INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/86798 Graphene-based catalysts (M-N-C) have emerged as an alternative to platinum catalysts in fuel cell cathodes due to their low cost and abundant availability. Among the graphene-based catalysts under investigation, the Mangan-Nikel dual-atom catalyst (DAC) shows potential as an alternative due to its good activity and stability. This study focuses on exploring and analyzing the oxygen reduction reaction (ORR) activity of the MnNiN6 catalyst by introducing nanopores so that the active sites are at the edge of graphene. This research uses density functional theory (DFT), the computational hydrogen electrode (CHE) approach, and microkinetic modeling, this research examines surface structure stability, ORR thermodynamics, and ORR kinetics for the MnNiN6 catalyst. The results show that the presence of nanopores can facilitate the formation of active sites, which is indicated by lower formation energy values compared to active sites in the base. The thermodynamic and kinetic analyses of the ORR on the MnNiN6 catalyst show consistent results. In the ortho configuration, the active site located on the edge of graphene with armchair type (MnNiN6)o@a1 shows an increase in ORR activity by 0.17 V compared to the basal configuration. Meanwhile, the para configuration shows an endergonic reaction at the OH* intermediate stage; nevertheless, the para surface with an OH*-poisoned active site demonstrates a high onset potential in configutarion (MnNiN6_OH)o@z1 reaching 0.53 V, an increase of 0.12 V from the basal site. These findings indicate that the presence of nanopores in graphene can enhance the ORR activity of the MnNiN6 catalyst in specific configurations. Keywords: Dual-Atom Catalyst (DAC), MnNiN6, DFT, ORR, fuel cell. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Graphene-based catalysts (M-N-C) have emerged as an alternative to platinum catalysts in fuel cell cathodes due to their low cost and abundant availability. Among the graphene-based catalysts under investigation, the Mangan-Nikel dual-atom catalyst (DAC) shows potential as an alternative due to its good activity and stability. This study focuses on exploring and analyzing the oxygen reduction reaction (ORR) activity of the MnNiN6 catalyst by introducing nanopores so that the active sites are at the edge of graphene. This research uses density functional theory (DFT), the computational hydrogen electrode (CHE) approach, and microkinetic modeling, this research examines surface structure stability, ORR thermodynamics, and ORR kinetics for the MnNiN6 catalyst. The results show that the presence of nanopores can facilitate the formation of active sites, which is indicated by lower formation energy values compared to active sites in the base. The thermodynamic and kinetic analyses of the ORR on the MnNiN6 catalyst show consistent results. In the ortho configuration, the active site located on the edge of graphene with armchair type (MnNiN6)o@a1 shows an increase in ORR activity by 0.17 V compared to the basal configuration. Meanwhile, the para configuration shows an endergonic reaction at the OH* intermediate stage; nevertheless, the para surface with an OH*-poisoned active site demonstrates a high onset potential in configutarion (MnNiN6_OH)o@z1 reaching 0.53 V, an increase of 0.12 V from the basal site. These findings indicate that the presence of nanopores in graphene can enhance the ORR activity of the MnNiN6 catalyst in specific configurations. Keywords: Dual-Atom Catalyst (DAC), MnNiN6, DFT, ORR, fuel cell.
format Theses
author Helmi, Faizal
spellingShingle Helmi, Faizal
MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS
author_facet Helmi, Faizal
author_sort Helmi, Faizal
title MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS
title_short MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS
title_full MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS
title_fullStr MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS
title_full_unstemmed MECHANISM OF OXYGEN REDUCTION REACTION ACTIVITY ON MANGAN-NIKEL DUAL-ATOM ELECTROCATALYST ACTIVE SITES LOCATED AT GRAPHENE NANOPORE EDGES FOR HYDROGEN FUEL CELL CATHODE APPLICATIONS
title_sort mechanism of oxygen reduction reaction activity on mangan-nikel dual-atom electrocatalyst active sites located at graphene nanopore edges for hydrogen fuel cell cathode applications
url https://digilib.itb.ac.id/gdl/view/86798
_version_ 1822283516080029696