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Graphene as an Imaging Platform of Charged Molecules
[Image: see text] Graphene, a single atom layer of carbon atoms, provides a two-dimensional platform with an extremely high sensitivity to charges due to its unique band structure and high surface-to-volume ratio. Graphene field-effect transistor (G-FET) biosensors have, indeed, demonstrated a detec...
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/PMC6044899/ https://www.ncbi.nlm.nih.gov/pubmed/30023861 http://dx.doi.org/10.1021/acsomega.7b02008 |
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author | Ushiba, Shota Ono, Takao Kanai, Yasushi Inoue, Koichi Kimura, Masahiko Matsumoto, Kazuhiko |
author_facet | Ushiba, Shota Ono, Takao Kanai, Yasushi Inoue, Koichi Kimura, Masahiko Matsumoto, Kazuhiko |
author_sort | Ushiba, Shota |
collection | PubMed |
description | [Image: see text] Graphene, a single atom layer of carbon atoms, provides a two-dimensional platform with an extremely high sensitivity to charges due to its unique band structure and high surface-to-volume ratio. Graphene field-effect transistor (G-FET) biosensors have, indeed, demonstrated a detection limit of subnanomolar or even subpicomolar. However, in G-FET, signal is averaged throughout the whole channel, so there remains a need to visualize the spatial distribution of target molecules on a single G-FET, to provide further insight into target molecules and/or biological functions. Here, we made use of graphene as an imaging platform of charged molecules via Raman microscopy. Positively (or negatively) charged microbeads with a diameter of 1 μm were dispersed in a buffer solution and were attached on graphene. We found out that Raman peaks of graphene, where positively (or negatively) charged beads contacted, were up-shifted (or down-shifted) significantly, indicating that the carrier density in the graphene was locally modulated by the charged beads and the charge state of the beads was represented by the peak-shift direction. From the peak shift, the change in the carrier density was calculated to be +1.4 × 10(12) cm(–2) (or −1.0 × 10(12) cm(–2)). By taking Raman peak-shift images, we visualized distribution of charged molecules on graphene with a spatial resolution below 1 μm. The technique described here overcomes the limitation of spatial resolution of G-FET and provides a new route to graphene-based chemical and biosensors. |
format | Online Article Text |
id | pubmed-6044899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60448992018-07-16 Graphene as an Imaging Platform of Charged Molecules Ushiba, Shota Ono, Takao Kanai, Yasushi Inoue, Koichi Kimura, Masahiko Matsumoto, Kazuhiko ACS Omega [Image: see text] Graphene, a single atom layer of carbon atoms, provides a two-dimensional platform with an extremely high sensitivity to charges due to its unique band structure and high surface-to-volume ratio. Graphene field-effect transistor (G-FET) biosensors have, indeed, demonstrated a detection limit of subnanomolar or even subpicomolar. However, in G-FET, signal is averaged throughout the whole channel, so there remains a need to visualize the spatial distribution of target molecules on a single G-FET, to provide further insight into target molecules and/or biological functions. Here, we made use of graphene as an imaging platform of charged molecules via Raman microscopy. Positively (or negatively) charged microbeads with a diameter of 1 μm were dispersed in a buffer solution and were attached on graphene. We found out that Raman peaks of graphene, where positively (or negatively) charged beads contacted, were up-shifted (or down-shifted) significantly, indicating that the carrier density in the graphene was locally modulated by the charged beads and the charge state of the beads was represented by the peak-shift direction. From the peak shift, the change in the carrier density was calculated to be +1.4 × 10(12) cm(–2) (or −1.0 × 10(12) cm(–2)). By taking Raman peak-shift images, we visualized distribution of charged molecules on graphene with a spatial resolution below 1 μm. The technique described here overcomes the limitation of spatial resolution of G-FET and provides a new route to graphene-based chemical and biosensors. American Chemical Society 2018-03-15 /pmc/articles/PMC6044899/ /pubmed/30023861 http://dx.doi.org/10.1021/acsomega.7b02008 Text en Copyright © 2018 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 | Ushiba, Shota Ono, Takao Kanai, Yasushi Inoue, Koichi Kimura, Masahiko Matsumoto, Kazuhiko Graphene as an Imaging Platform of Charged Molecules |
title | Graphene as an Imaging Platform of Charged Molecules |
title_full | Graphene as an Imaging Platform of Charged Molecules |
title_fullStr | Graphene as an Imaging Platform of Charged Molecules |
title_full_unstemmed | Graphene as an Imaging Platform of Charged Molecules |
title_short | Graphene as an Imaging Platform of Charged Molecules |
title_sort | graphene as an imaging platform of charged molecules |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044899/ https://www.ncbi.nlm.nih.gov/pubmed/30023861 http://dx.doi.org/10.1021/acsomega.7b02008 |
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