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DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation

[Image: see text] Direct methanol fuel cell technology implementation mainly depends on the development of non-platinum catalysts with good CO tolerance. Among the widely studied transition-metal catalysts, cobalt oxide with distinctively higher catalytic efficiency is highly desirable. Here, we hav...

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Autores principales: Kumaravel, Sangeetha, Subramanian, Mohanapriya, Karthick, Kannimuthu, Sakthivel, Arunkumar, Kundu, Subrata, Alwarappan, Subbiah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320070/
https://www.ncbi.nlm.nih.gov/pubmed/34337254
http://dx.doi.org/10.1021/acsomega.1c02515
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author Kumaravel, Sangeetha
Subramanian, Mohanapriya
Karthick, Kannimuthu
Sakthivel, Arunkumar
Kundu, Subrata
Alwarappan, Subbiah
author_facet Kumaravel, Sangeetha
Subramanian, Mohanapriya
Karthick, Kannimuthu
Sakthivel, Arunkumar
Kundu, Subrata
Alwarappan, Subbiah
author_sort Kumaravel, Sangeetha
collection PubMed
description [Image: see text] Direct methanol fuel cell technology implementation mainly depends on the development of non-platinum catalysts with good CO tolerance. Among the widely studied transition-metal catalysts, cobalt oxide with distinctively higher catalytic efficiency is highly desirable. Here, we have evolved a simple method of synthesizing cobalt tungsten oxide hydroxide hydrate nanowires with DNA (CTOOH/DNA) and without incorporating DNA (CTOOH) by microwave irradiation and subsequently employed them as electrocatalysts for methanol oxidation. Following this, we examined the influence of incorporating DNA into CTOOH by cyclic voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. The enhanced electrochemical surface area of CTOOH offered readily available electroactive sites and resulted in a higher oxidation current at a lower onset potential for methanol oxidation. On the other hand, CTOOH/DNA exhibited improved CO tolerance and it was evident from the chronoamperometric studies. Herein, we noticed only a 2.5 and 1.8% drop at CTOOH- and CTOOH/DNA-modified electrodes, respectively, after 30 min. Overall, from the results, it was evident that the presence of DNA in CTOOH played an important role in the rapid removal of adsorbed intermediates and regenerated active catalyst centers possibly by creating high density surface defects around the nanochains than bare CTOOH.
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spelling pubmed-83200702021-07-30 DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation Kumaravel, Sangeetha Subramanian, Mohanapriya Karthick, Kannimuthu Sakthivel, Arunkumar Kundu, Subrata Alwarappan, Subbiah ACS Omega [Image: see text] Direct methanol fuel cell technology implementation mainly depends on the development of non-platinum catalysts with good CO tolerance. Among the widely studied transition-metal catalysts, cobalt oxide with distinctively higher catalytic efficiency is highly desirable. Here, we have evolved a simple method of synthesizing cobalt tungsten oxide hydroxide hydrate nanowires with DNA (CTOOH/DNA) and without incorporating DNA (CTOOH) by microwave irradiation and subsequently employed them as electrocatalysts for methanol oxidation. Following this, we examined the influence of incorporating DNA into CTOOH by cyclic voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. The enhanced electrochemical surface area of CTOOH offered readily available electroactive sites and resulted in a higher oxidation current at a lower onset potential for methanol oxidation. On the other hand, CTOOH/DNA exhibited improved CO tolerance and it was evident from the chronoamperometric studies. Herein, we noticed only a 2.5 and 1.8% drop at CTOOH- and CTOOH/DNA-modified electrodes, respectively, after 30 min. Overall, from the results, it was evident that the presence of DNA in CTOOH played an important role in the rapid removal of adsorbed intermediates and regenerated active catalyst centers possibly by creating high density surface defects around the nanochains than bare CTOOH. American Chemical Society 2021-07-13 /pmc/articles/PMC8320070/ /pubmed/34337254 http://dx.doi.org/10.1021/acsomega.1c02515 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Kumaravel, Sangeetha
Subramanian, Mohanapriya
Karthick, Kannimuthu
Sakthivel, Arunkumar
Kundu, Subrata
Alwarappan, Subbiah
DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation
title DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation
title_full DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation
title_fullStr DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation
title_full_unstemmed DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation
title_short DNA-Modified Cobalt Tungsten Oxide Hydroxide Hydrate Nanochains as an Effective Electrocatalyst with Amplified CO Tolerance during Methanol Oxidation
title_sort dna-modified cobalt tungsten oxide hydroxide hydrate nanochains as an effective electrocatalyst with amplified co tolerance during methanol oxidation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320070/
https://www.ncbi.nlm.nih.gov/pubmed/34337254
http://dx.doi.org/10.1021/acsomega.1c02515
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