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The Nucleation Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes
[Image: see text] Nanobubble nucleation is a problem that affects efficiency in electrocatalytic reactions since those bubbles can block the surface of the catalytic sites. In this article, we focus on the nucleation rate of O(2) nanobubbles resulting from the electrooxidation of H(2)O(2) at Pt disk...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150736/ https://www.ncbi.nlm.nih.gov/pubmed/29847948 http://dx.doi.org/10.1021/acs.langmuir.8b01372 |
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author | Soto, Álvaro Moreno German, Sean R. Ren, Hang van der Meer, Devaraj Lohse, Detlef Edwards, Martin A. White, Henry S. |
author_facet | Soto, Álvaro Moreno German, Sean R. Ren, Hang van der Meer, Devaraj Lohse, Detlef Edwards, Martin A. White, Henry S. |
author_sort | Soto, Álvaro Moreno |
collection | PubMed |
description | [Image: see text] Nanobubble nucleation is a problem that affects efficiency in electrocatalytic reactions since those bubbles can block the surface of the catalytic sites. In this article, we focus on the nucleation rate of O(2) nanobubbles resulting from the electrooxidation of H(2)O(2) at Pt disk nanoelectrodes. Bubbles form almost instantaneously when a critical peak current, i(nb)(p), is applied, but for lower currents, bubble nucleation is a stochastic process in which the nucleation (induction) time, t(ind), dramatically decreases as the applied current approaches i(nb)(p), a consequence of the local supersaturation level, ζ, increasing at high currents. Here, by applying different currents below i(nb)(p), nanobubbles take some time to nucleate and block the surface of the Pt electrode at which the reaction occurs, providing a means to measure the stochastic t(ind). We study in detail the different conditions in which nanobubbles appear, concluding that the electrode surface needs to be preconditioned to achieve reproducible results. We also measure the activation energy for bubble nucleation, E(a), which varies in the range from (6 to 30)kT, and assuming a spherically cap-shaped nanobubble nucleus, we determine the footprint diameter L = 8–15 nm, the contact angle to the electrode surface θ = 135–155°, and the number of O(2) molecules contained in the nucleus (50 to 900 molecules). |
format | Online Article Text |
id | pubmed-6150736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61507362018-09-24 The Nucleation Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes Soto, Álvaro Moreno German, Sean R. Ren, Hang van der Meer, Devaraj Lohse, Detlef Edwards, Martin A. White, Henry S. Langmuir [Image: see text] Nanobubble nucleation is a problem that affects efficiency in electrocatalytic reactions since those bubbles can block the surface of the catalytic sites. In this article, we focus on the nucleation rate of O(2) nanobubbles resulting from the electrooxidation of H(2)O(2) at Pt disk nanoelectrodes. Bubbles form almost instantaneously when a critical peak current, i(nb)(p), is applied, but for lower currents, bubble nucleation is a stochastic process in which the nucleation (induction) time, t(ind), dramatically decreases as the applied current approaches i(nb)(p), a consequence of the local supersaturation level, ζ, increasing at high currents. Here, by applying different currents below i(nb)(p), nanobubbles take some time to nucleate and block the surface of the Pt electrode at which the reaction occurs, providing a means to measure the stochastic t(ind). We study in detail the different conditions in which nanobubbles appear, concluding that the electrode surface needs to be preconditioned to achieve reproducible results. We also measure the activation energy for bubble nucleation, E(a), which varies in the range from (6 to 30)kT, and assuming a spherically cap-shaped nanobubble nucleus, we determine the footprint diameter L = 8–15 nm, the contact angle to the electrode surface θ = 135–155°, and the number of O(2) molecules contained in the nucleus (50 to 900 molecules). American Chemical Society 2018-05-30 2018-06-26 /pmc/articles/PMC6150736/ /pubmed/29847948 http://dx.doi.org/10.1021/acs.langmuir.8b01372 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Soto, Álvaro Moreno German, Sean R. Ren, Hang van der Meer, Devaraj Lohse, Detlef Edwards, Martin A. White, Henry S. The Nucleation Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes |
title | The Nucleation
Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes |
title_full | The Nucleation
Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes |
title_fullStr | The Nucleation
Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes |
title_full_unstemmed | The Nucleation
Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes |
title_short | The Nucleation
Rate of Single O(2) Nanobubbles at Pt Nanoelectrodes |
title_sort | nucleation
rate of single o(2) nanobubbles at pt nanoelectrodes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150736/ https://www.ncbi.nlm.nih.gov/pubmed/29847948 http://dx.doi.org/10.1021/acs.langmuir.8b01372 |
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