2018
DOI: 10.1063/1.5021959
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Effect of channel-width and chirality on graphene field-effect transistor based real-time biomolecule sensing

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Cited by 4 publications
(9 citation statements)
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“…In real-time biosensing, the sensitivity can be quantified by the percent age change of FET current, dI DS /I DS [37]. To maximize dI DS /I DS we need to co-optimize the FET transconductance (g m ) and the total gate capacitance C G [25]. A highly sensitive GFET typically features a low limit of detection (LOD), defined as the lowest amount of targeted bio-molecules or cell-released chemicals, named as bio-target here, with a statistically significant FET readout (see the definition of signal to background ratio below).…”
Section: Overview Of the Device Concepts And Research Statusmentioning
confidence: 99%
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“…In real-time biosensing, the sensitivity can be quantified by the percent age change of FET current, dI DS /I DS [37]. To maximize dI DS /I DS we need to co-optimize the FET transconductance (g m ) and the total gate capacitance C G [25]. A highly sensitive GFET typically features a low limit of detection (LOD), defined as the lowest amount of targeted bio-molecules or cell-released chemicals, named as bio-target here, with a statistically significant FET readout (see the definition of signal to background ratio below).…”
Section: Overview Of the Device Concepts And Research Statusmentioning
confidence: 99%
“…For instance, in real-time biosensing SBR can be defined as the percentage of the FET current change, ΔI DS /I DS , between the current values before and after adding the bio-targets to GFETs (e.g. molecule absorption or cell signaling) [25,37]. The background signal (i.e.…”
Section: Overview Of the Device Concepts And Research Statusmentioning
confidence: 99%
See 3 more Smart Citations