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Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement
With the development of new instruments and methodologies, the highly dynamic behaviors of nanoparticle at the liquid-solid interface have been studied. However, the dynamic nature of the electrochemical behavior of individual nanoparticles on the electrode interface is still poorly understood. Here...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210955/ https://www.ncbi.nlm.nih.gov/pubmed/32385284 http://dx.doi.org/10.1038/s41467-020-16149-0 |
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author | Ma, Hui Chen, Jian-Fu Wang, Hai-Feng Hu, Pei-Jun Ma, Wei Long, Yi-Tao |
author_facet | Ma, Hui Chen, Jian-Fu Wang, Hai-Feng Hu, Pei-Jun Ma, Wei Long, Yi-Tao |
author_sort | Ma, Hui |
collection | PubMed |
description | With the development of new instruments and methodologies, the highly dynamic behaviors of nanoparticle at the liquid-solid interface have been studied. However, the dynamic nature of the electrochemical behavior of individual nanoparticles on the electrode interface is still poorly understood. Here, we generalize scaling relations to predict nanoparticle-electrode interactions by examining the adsorption energy of nanoparticles at an ultramicroelectrode interface. Based on the theoretical predictions, we investigate the interaction-modulated dynamic electrochemical behaviors for the oxidation of individual Ag nanoparticles. Typically, significantly distinct current traces are observed owing to the adsorption-mediated motion of Ag nanoparticles. Inspired by restraining the stochastic paths of particles in the vicinity of the electrode interface to produce surface-confined current traces, we successfully realize high-resolution size measurements of Ag nanoparticles in mixed-sample systems. This work offers a better understanding of dynamic interactions of nanoparticles at the electrochemical interface and displays highly valuable applications of single-entity electrochemistry. |
format | Online Article Text |
id | pubmed-7210955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72109552020-05-13 Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement Ma, Hui Chen, Jian-Fu Wang, Hai-Feng Hu, Pei-Jun Ma, Wei Long, Yi-Tao Nat Commun Article With the development of new instruments and methodologies, the highly dynamic behaviors of nanoparticle at the liquid-solid interface have been studied. However, the dynamic nature of the electrochemical behavior of individual nanoparticles on the electrode interface is still poorly understood. Here, we generalize scaling relations to predict nanoparticle-electrode interactions by examining the adsorption energy of nanoparticles at an ultramicroelectrode interface. Based on the theoretical predictions, we investigate the interaction-modulated dynamic electrochemical behaviors for the oxidation of individual Ag nanoparticles. Typically, significantly distinct current traces are observed owing to the adsorption-mediated motion of Ag nanoparticles. Inspired by restraining the stochastic paths of particles in the vicinity of the electrode interface to produce surface-confined current traces, we successfully realize high-resolution size measurements of Ag nanoparticles in mixed-sample systems. This work offers a better understanding of dynamic interactions of nanoparticles at the electrochemical interface and displays highly valuable applications of single-entity electrochemistry. Nature Publishing Group UK 2020-05-08 /pmc/articles/PMC7210955/ /pubmed/32385284 http://dx.doi.org/10.1038/s41467-020-16149-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ma, Hui Chen, Jian-Fu Wang, Hai-Feng Hu, Pei-Jun Ma, Wei Long, Yi-Tao Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
title | Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
title_full | Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
title_fullStr | Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
title_full_unstemmed | Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
title_short | Exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
title_sort | exploring dynamic interactions of single nanoparticles at interfaces for surface-confined electrochemical behavior and size measurement |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210955/ https://www.ncbi.nlm.nih.gov/pubmed/32385284 http://dx.doi.org/10.1038/s41467-020-16149-0 |
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