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Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors
Understanding the hybrid charge-storage mechanisms of pseudocapacitive nanomaterials holds promising keys to further improve the performance of energy storage devices. Based on the dependence of the light scattering intensity of single Prussian blue nanoparticles (PBNPs) on their oxidation state dur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051208/ https://www.ncbi.nlm.nih.gov/pubmed/35484125 http://dx.doi.org/10.1038/s41467-022-30058-4 |
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author | Niu, Ben Jiang, Wenxuan Jiang, Bo Lv, Mengqi Wang, Sa Wang, Wei |
author_facet | Niu, Ben Jiang, Wenxuan Jiang, Bo Lv, Mengqi Wang, Sa Wang, Wei |
author_sort | Niu, Ben |
collection | PubMed |
description | Understanding the hybrid charge-storage mechanisms of pseudocapacitive nanomaterials holds promising keys to further improve the performance of energy storage devices. Based on the dependence of the light scattering intensity of single Prussian blue nanoparticles (PBNPs) on their oxidation state during sinusoidal potential modulation at varying frequencies, we present an electro-optical microscopic imaging approach to optically acquire the Faradaic electrochemical impedance spectroscopy (oEIS) of single PBNPs. Here we reveal typical pseudocapacitive behavior with hybrid charge-storage mechanisms depending on the modulation frequency. In the low-frequency range, the optical amplitude is inversely proportional to the square root of the frequency (∆I ∝ f(−0.5); diffusion-limited process), while in the high-frequency range, it is inversely proportional to the frequency (∆I ∝ f(−1); surface charging process). Because the geometry of single cuboid-shaped PBNPs can be precisely determined by scanning electron microscopy and atomic force microscopy, oEIS of single PBNPs allows the determination of the depth of the surface charging layer, revealing it to be ~2 unit cells regardless of the nanoparticle size. |
format | Online Article Text |
id | pubmed-9051208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90512082022-04-30 Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors Niu, Ben Jiang, Wenxuan Jiang, Bo Lv, Mengqi Wang, Sa Wang, Wei Nat Commun Article Understanding the hybrid charge-storage mechanisms of pseudocapacitive nanomaterials holds promising keys to further improve the performance of energy storage devices. Based on the dependence of the light scattering intensity of single Prussian blue nanoparticles (PBNPs) on their oxidation state during sinusoidal potential modulation at varying frequencies, we present an electro-optical microscopic imaging approach to optically acquire the Faradaic electrochemical impedance spectroscopy (oEIS) of single PBNPs. Here we reveal typical pseudocapacitive behavior with hybrid charge-storage mechanisms depending on the modulation frequency. In the low-frequency range, the optical amplitude is inversely proportional to the square root of the frequency (∆I ∝ f(−0.5); diffusion-limited process), while in the high-frequency range, it is inversely proportional to the frequency (∆I ∝ f(−1); surface charging process). Because the geometry of single cuboid-shaped PBNPs can be precisely determined by scanning electron microscopy and atomic force microscopy, oEIS of single PBNPs allows the determination of the depth of the surface charging layer, revealing it to be ~2 unit cells regardless of the nanoparticle size. Nature Publishing Group UK 2022-04-28 /pmc/articles/PMC9051208/ /pubmed/35484125 http://dx.doi.org/10.1038/s41467-022-30058-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Niu, Ben Jiang, Wenxuan Jiang, Bo Lv, Mengqi Wang, Sa Wang, Wei Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors |
title | Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors |
title_full | Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors |
title_fullStr | Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors |
title_full_unstemmed | Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors |
title_short | Determining the depth of surface charging layer of single Prussian blue nanoparticles with pseudocapacitive behaviors |
title_sort | determining the depth of surface charging layer of single prussian blue nanoparticles with pseudocapacitive behaviors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051208/ https://www.ncbi.nlm.nih.gov/pubmed/35484125 http://dx.doi.org/10.1038/s41467-022-30058-4 |
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