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Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process

[Image: see text] Polyvinylpyrrolidone (PVP)-assisted nanocatalyst preparation was succeeded by employing a controlled solvothermal route to produce efficient electrodes for electrochemical water-splitting applications. Bi(2)WO(6) and FeWO(4) nanocatalysts have been confirmed through the strong sign...

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Autores principales: Jansi Rani, Balasubramanian, Ravi, Ganesan, Yuvakkumar, Rathinam, Praveenkumar, M., Ravichandran, Subbiah, Muthu Mareeswaran, Paulpandian, Hong, Sun Ig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648914/
https://www.ncbi.nlm.nih.gov/pubmed/31459696
http://dx.doi.org/10.1021/acsomega.8b03003
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author Jansi Rani, Balasubramanian
Ravi, Ganesan
Yuvakkumar, Rathinam
Praveenkumar, M.
Ravichandran, Subbiah
Muthu Mareeswaran, Paulpandian
Hong, Sun Ig
author_facet Jansi Rani, Balasubramanian
Ravi, Ganesan
Yuvakkumar, Rathinam
Praveenkumar, M.
Ravichandran, Subbiah
Muthu Mareeswaran, Paulpandian
Hong, Sun Ig
author_sort Jansi Rani, Balasubramanian
collection PubMed
description [Image: see text] Polyvinylpyrrolidone (PVP)-assisted nanocatalyst preparation was succeeded by employing a controlled solvothermal route to produce efficient electrodes for electrochemical water-splitting applications. Bi(2)WO(6) and FeWO(4) nanocatalysts have been confirmed through the strong signature of (113) and (111) crystal planes, respectively. The binding natures of Bi–W–O and Fe–W–O have been thoroughly discussed by employing X-ray photoelectron spectroscopy which confirmed the formation of Bi(2)WO(6) and FeWO(4). The freestanding nanoplate array morphology of Bi(2)WO(6) and the fine nanosphere particle morphology of FeWO(4) nanocatalysts were revealed by scanning electron microscopy images. With these confirmations, the fabrication of durable, long-term electrodes for electrochemical water splitting has been subjected to efficient oxidation of water, confirmed by obtaining 2.79 and 1.96 mA/g for 0.5 g PVP-assisted Bi(2)WO(6) and FeWO(4) nanocatalysts, respectively. The water oxidation mechanism of both nanocatalysts has been revealed with the support of 24 h stability test over continuous water oxidation and faster charge transfer achieved by the smaller Tafel slope values of 75 and 78 mV/dec, respectively. Generally, these nanocatalysts are utilized for photocatalytic applications. The present study revealed the PVP-assisted synthesis to produce electrocatalytically active nanocatalysts and their electrochemical water-splitting mechanism which will offer a pathway for research interests with regard to the production of multifunctional nanocatalysts for both electro- and photocatalytic applications in the near future.
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spelling pubmed-66489142019-08-27 Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process Jansi Rani, Balasubramanian Ravi, Ganesan Yuvakkumar, Rathinam Praveenkumar, M. Ravichandran, Subbiah Muthu Mareeswaran, Paulpandian Hong, Sun Ig ACS Omega [Image: see text] Polyvinylpyrrolidone (PVP)-assisted nanocatalyst preparation was succeeded by employing a controlled solvothermal route to produce efficient electrodes for electrochemical water-splitting applications. Bi(2)WO(6) and FeWO(4) nanocatalysts have been confirmed through the strong signature of (113) and (111) crystal planes, respectively. The binding natures of Bi–W–O and Fe–W–O have been thoroughly discussed by employing X-ray photoelectron spectroscopy which confirmed the formation of Bi(2)WO(6) and FeWO(4). The freestanding nanoplate array morphology of Bi(2)WO(6) and the fine nanosphere particle morphology of FeWO(4) nanocatalysts were revealed by scanning electron microscopy images. With these confirmations, the fabrication of durable, long-term electrodes for electrochemical water splitting has been subjected to efficient oxidation of water, confirmed by obtaining 2.79 and 1.96 mA/g for 0.5 g PVP-assisted Bi(2)WO(6) and FeWO(4) nanocatalysts, respectively. The water oxidation mechanism of both nanocatalysts has been revealed with the support of 24 h stability test over continuous water oxidation and faster charge transfer achieved by the smaller Tafel slope values of 75 and 78 mV/dec, respectively. Generally, these nanocatalysts are utilized for photocatalytic applications. The present study revealed the PVP-assisted synthesis to produce electrocatalytically active nanocatalysts and their electrochemical water-splitting mechanism which will offer a pathway for research interests with regard to the production of multifunctional nanocatalysts for both electro- and photocatalytic applications in the near future. American Chemical Society 2019-03-13 /pmc/articles/PMC6648914/ /pubmed/31459696 http://dx.doi.org/10.1021/acsomega.8b03003 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Jansi Rani, Balasubramanian
Ravi, Ganesan
Yuvakkumar, Rathinam
Praveenkumar, M.
Ravichandran, Subbiah
Muthu Mareeswaran, Paulpandian
Hong, Sun Ig
Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process
title Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process
title_full Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process
title_fullStr Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process
title_full_unstemmed Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process
title_short Bi(2)WO(6) and FeWO(4) Nanocatalysts for the Electrochemical Water Oxidation Process
title_sort bi(2)wo(6) and fewo(4) nanocatalysts for the electrochemical water oxidation process
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648914/
https://www.ncbi.nlm.nih.gov/pubmed/31459696
http://dx.doi.org/10.1021/acsomega.8b03003
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