Tailor-designed nanowire-structured iron and nickel oxides on platinum catalyst for formic acid electro-oxidation
This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeO x ) and nickel (nano-NiO x ) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-...
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Published in | RSC advances Vol. 12; no. 31; pp. 2395 - 242 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
06.07.2022
The Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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Abstract | This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeO
x
) and nickel (nano-NiO
x
) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiO
x
appeared as fibrillar nanowire bundles (
ca.
82 nm and 4.2 μm average diameter and length, respectively), nano-FeO
x
was deposited as intersecting nanowires (
ca.
74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeO
x
/NiO
x
/Pt catalyst exhibited
ca.
4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeO
x
/NiO
x
/Pt catalyst at −0.5 V
vs.
Ag/AgCl/KCl (sat.) in 0.2 mol L
−1
NaOH, a favorable Fe
2+
/Fe
3+
transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeO
x
/NiO
x
/Pt catalyst had an activity 7 times higher than that of bare-Pt with an
ca.
−122 mV shift in the onset potential of the FAOR. The presence of nano-FeO
x
and nano-NiO
x
enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra.
A FeO
x
/NiO
x
/Pt catalyst was recommended for formic acid electro-oxidation; the essential anodic reaction in direct formic acid fuel cells. |
---|---|
AbstractList | This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeO
x
) and nickel (nano-NiO
x
) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiO
x
appeared as fibrillar nanowire bundles (
ca.
82 nm and 4.2 μm average diameter and length, respectively), nano-FeO
x
was deposited as intersecting nanowires (
ca.
74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeO
x
/NiO
x
/Pt catalyst exhibited
ca.
4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeO
x
/NiO
x
/Pt catalyst at −0.5 V
vs.
Ag/AgCl/KCl (sat.) in 0.2 mol L
−1
NaOH, a favorable Fe
2+
/Fe
3+
transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeO
x
/NiO
x
/Pt catalyst had an activity 7 times higher than that of bare-Pt with an
ca.
−122 mV shift in the onset potential of the FAOR. The presence of nano-FeO
x
and nano-NiO
x
enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra.
A FeO
x
/NiO
x
/Pt catalyst was recommended for formic acid electro-oxidation; the essential anodic reaction in direct formic acid fuel cells. This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeOx) and nickel (nano-NiOx) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiOx appeared as fibrillar nanowire bundles (ca. 82 nm and 4.2 μm average diameter and length, respectively), nano-FeOx was deposited as intersecting nanowires (ca. 74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeOx/NiOx/Pt catalyst exhibited ca. 4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeOx/NiOx/Pt catalyst at −0.5 V vs. Ag/AgCl/KCl (sat.) in 0.2 mol L−1 NaOH, a favorable Fe2+/Fe3+ transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeOx/NiOx/Pt catalyst had an activity 7 times higher than that of bare-Pt with an ca. −122 mV shift in the onset potential of the FAOR. The presence of nano-FeOx and nano-NiOx enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra. This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeO x ) and nickel (nano-NiO x ) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiO x appeared as fibrillar nanowire bundles ( ca. 82 nm and 4.2 μm average diameter and length, respectively), nano-FeO x was deposited as intersecting nanowires ( ca. 74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeO x /NiO x /Pt catalyst exhibited ca. 4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeO x /NiO x /Pt catalyst at −0.5 V vs. Ag/AgCl/KCl (sat.) in 0.2 mol L −1 NaOH, a favorable Fe 2+ /Fe 3+ transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeO x /NiO x /Pt catalyst had an activity 7 times higher than that of bare-Pt with an ca. −122 mV shift in the onset potential of the FAOR. The presence of nano-FeO x and nano-NiO x enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra. |
Author | Alalawy, Hafsa H Allam, Nageh K Al-Akraa, Islam M Al-Qodami, Bilquis Ali Sayed, Sayed Youssef Mohammad, Ahmad M |
AuthorAffiliation | The British University in Egypt Chemistry Department Energy Materials Laboratory Hajjah University The American University in Cairo Faculty of Engineering Department of Chemical Engineering Faculty of Science Faculty of Education and Applied Science School of Sciences and Engineering Cairo University |
AuthorAffiliation_xml | – name: Department of Chemical Engineering – name: Faculty of Engineering – name: Energy Materials Laboratory – name: School of Sciences and Engineering – name: Chemistry Department – name: Faculty of Education and Applied Science – name: Cairo University – name: The British University in Egypt – name: Faculty of Science – name: The American University in Cairo – name: Hajjah University |
Author_xml | – sequence: 1 givenname: Bilquis Ali surname: Al-Qodami fullname: Al-Qodami, Bilquis Ali – sequence: 2 givenname: Hafsa H surname: Alalawy fullname: Alalawy, Hafsa H – sequence: 3 givenname: Sayed Youssef surname: Sayed fullname: Sayed, Sayed Youssef – sequence: 4 givenname: Islam M surname: Al-Akraa fullname: Al-Akraa, Islam M – sequence: 5 givenname: Nageh K surname: Allam fullname: Allam, Nageh K – sequence: 6 givenname: Ahmad M surname: Mohammad fullname: Mohammad, Ahmad M |
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CitedBy_id | crossref_primary_10_1039_D2CC05955J crossref_primary_10_1039_D3RA03350C crossref_primary_10_1016_j_arabjc_2022_104524 crossref_primary_10_1016_j_egyr_2022_10_232 crossref_primary_10_1016_j_aej_2023_06_069 crossref_primary_10_12677_JAPC_2023_124028 |
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Snippet | This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeO
x
) and... This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeOx) and nickel... |
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SubjectTerms | Carbon monoxide Carbon monoxide poisoning Catalysts Catalytic activity Chemistry Formic acid Fuel cells Iron Nanowires Nickel Oxidation Oxygen enrichment Platinum Poisoning Substrates |
Title | Tailor-designed nanowire-structured iron and nickel oxides on platinum catalyst for formic acid electro-oxidation |
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