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In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium
In situ electrochemical activation as a new pre-treatment method is extremely effective for enhanced electrocatalytic performances for different applications. With the help of this method, in situ surface modification of electrocatalyst is achieved without using pre-made seeds or complex synthesis p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695632/ https://www.ncbi.nlm.nih.gov/pubmed/35423543 http://dx.doi.org/10.1039/d0ra07817d |
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author | Kardan, Alireza Ashraf, Narges Dabirifar, Zeynab Khadempir, Sara |
author_facet | Kardan, Alireza Ashraf, Narges Dabirifar, Zeynab Khadempir, Sara |
author_sort | Kardan, Alireza |
collection | PubMed |
description | In situ electrochemical activation as a new pre-treatment method is extremely effective for enhanced electrocatalytic performances for different applications. With the help of this method, in situ surface modification of electrocatalyst is achieved without using pre-made seeds or complex synthesis procedure. Herein, with the purpose of finding an in situ and simple electrochemical activation protocol, the green synthesis of Au/Pd nanoparticles (AuPd) by means of polyoxometalate (POM) is reported. Structural analysis of the AuPd nanohybrid unveil the Au-core/Pd-shell structure which surrounded by POM. We propose a novel cathodic electrochemical activation in phosphate buffer solution which can greatly boost the electrocatalytic activity of the as-prepared AuPd and Pd electrocatalyst not only for hydrogen evolution reaction (HER) as a model of electro-reduction, but also for methanol and ethanol electro-oxidation reaction (MOR & EOR). For the HER in 1 M NaOH solution, after the electrochemical activation, the needed potential to drive a geometrical current density of 10 mA cm(−2) significantly decreases from – 400 mV vs. the reversible hydrogen electrode (RHE) to −290 mV vs. RHE. For the EOR and MOR, electrochemically activated AuPd realized 3.4- and 2.9- fold increase in mass current density (mA mg(Pd)(−1)) with respect to the pristine AuPd electrocatalyst, respectively. |
format | Online Article Text |
id | pubmed-8695632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86956322022-04-13 In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium Kardan, Alireza Ashraf, Narges Dabirifar, Zeynab Khadempir, Sara RSC Adv Chemistry In situ electrochemical activation as a new pre-treatment method is extremely effective for enhanced electrocatalytic performances for different applications. With the help of this method, in situ surface modification of electrocatalyst is achieved without using pre-made seeds or complex synthesis procedure. Herein, with the purpose of finding an in situ and simple electrochemical activation protocol, the green synthesis of Au/Pd nanoparticles (AuPd) by means of polyoxometalate (POM) is reported. Structural analysis of the AuPd nanohybrid unveil the Au-core/Pd-shell structure which surrounded by POM. We propose a novel cathodic electrochemical activation in phosphate buffer solution which can greatly boost the electrocatalytic activity of the as-prepared AuPd and Pd electrocatalyst not only for hydrogen evolution reaction (HER) as a model of electro-reduction, but also for methanol and ethanol electro-oxidation reaction (MOR & EOR). For the HER in 1 M NaOH solution, after the electrochemical activation, the needed potential to drive a geometrical current density of 10 mA cm(−2) significantly decreases from – 400 mV vs. the reversible hydrogen electrode (RHE) to −290 mV vs. RHE. For the EOR and MOR, electrochemically activated AuPd realized 3.4- and 2.9- fold increase in mass current density (mA mg(Pd)(−1)) with respect to the pristine AuPd electrocatalyst, respectively. The Royal Society of Chemistry 2021-03-12 /pmc/articles/PMC8695632/ /pubmed/35423543 http://dx.doi.org/10.1039/d0ra07817d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Kardan, Alireza Ashraf, Narges Dabirifar, Zeynab Khadempir, Sara In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
title |
In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
title_full |
In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
title_fullStr |
In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
title_full_unstemmed |
In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
title_short |
In situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
title_sort | in situ electrochemical activation as a generic strategy for promoting the electrocatalytic hydrogen evolution reaction and alcohol electro-oxidation in alkaline medium |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695632/ https://www.ncbi.nlm.nih.gov/pubmed/35423543 http://dx.doi.org/10.1039/d0ra07817d |
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