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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...

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Autores principales: Ushiba, Shota, Ono, Takao, Kanai, Yasushi, Inoue, Koichi, Kimura, Masahiko, Matsumoto, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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