Abstract
AbstractSolution Gated Graphene Field‐Effect Transistors (SGGT) are eagerly anticipated as an amplification platform for fabricating advanced ultra‐sensitive sensors, allowing significant modulation of the drain current with minimal gate voltage. However, few studies have focused on light‐matter interplay gating control for SGGT. Herein, this challenge is addressed by creating an innovative photoelectrochemical solution‐gated graphene field‐effect transistor (PEC‐SGGT) functionalized with enzyme cascade reactions (ECR) for Organophosphorus (OPs) detection. The ECR system, consisting of acetylcholinesterase (AChE) and CuBTC nanomimetic enzymes, selectively recognizes OPs and forms o‐phenylenediamine (oPD) oligomers sediment on the PEC electrode, with layer thickness related to the OPs concentration, demonstrating time‐integrated amplification. Under light stimulation, the additional photovoltage generated on the PEC gate electrode is influenced by the oPD oligomers sediment layer, creating a differentiated voltage distribution along the gate path. PEC‐SGGT, inherently equipped with built‐in amplification circuits, sensitively captures gate voltage changes and delivers output with an impressive thousandfold current gain. The seamless integration of these three amplification modes in this advanced sensor allows a good linear range and highly sensitive detection of OPs, with a detection limit as low as 0.05 pm. This work provides a proof‐of‐concept for the feasibility of light‐assisted functionalized gate‐controlled PEC‐SGGT for small molecule detection.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.