Detection of lysine molecular ions in solution gated field effect transistors based on unmodified graphene
The electrical transport in graphene interfaced with different ions in solution gated graphene field effect transistors (GFETs) is the subject of active studies due to its importance in sensor fabrication. Most of the developed GFET biological sensors use graphene that has been modified. The difficu...
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Published in | Journal of applied physics Vol. 128; no. 21 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Melville
American Institute of Physics
07.12.2020
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Subjects | |
Online Access | Get full text |
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Summary: | The electrical transport in graphene interfaced with different ions in solution gated graphene field effect transistors (GFETs) is the subject of active studies due to its importance in sensor fabrication. Most of the developed GFET biological sensors use graphene that has been modified. The difficulty in the modification procedure and the reduction in quality of graphene that it causes are important drawbacks for applications. Therefore, we focus on GFETs based on unmodified graphene gated by aqueous solutions containing lysine amino acids. We observed that an increase in the ionic concentration of lysine in these solutions leads to a suppression of unipolar electron conductance of graphene in GFETs. This dependence is opposite to the dependence typically observed in gating solutions containing smaller atomic ions. We attribute the observed suppression to electric field screening of the graphene surface from water molecules by lysine ions which are larger and have lower charge density compared to atomic ions. This novel phenomenon leads to an overall decrease of surface charge density in molecular layers formed at the graphene interface and can be applied in GFET sensors with unmodified graphene that detect the presence and concentration of large molecules in the gating solutions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 0021-8979 1089-7550 |
DOI: | 10.1063/5.0028108 |