Deriving a novel methodology for Nano-BioFETs and analyzing the effect of high-k oxides on the amino-acids sensing application

19 April 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

In this paper, a novel methodology is presented with the analytical simulations of BioFETs using the Gouy-Chapman-Stern and Modified Site-binding model. The derived approach is used to detect different amino acids such as Arginine (R), Aspartic Acid (D) and Proline (P), functionalized with the help of a linker over the gate-oxide. The performance of the BioFETs is optimized while analyzing the effect of high-k dielectrics as the gate oxide. High-k oxides are responsible for tuning the parameters such as sensitivity, surface potential and intrinsic buffer capacity. The variation of differential capacitance with the second gradient of drain current and surface potential are used to identify the signatures of different amino acids. The proposed method can be helpful in defining an efficient method for protein sequencing.

Keywords

ISFET
nano-biosensing
Amino Acids
Gouy-Chapman-Stern Theory
Modified Site-Binding Theory
PMI
TCAD simulation
High-k

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.