Reversible ppt-Level Detection of Perfluorooctane Sulfonic Acid in Tap Water using Field-Effect Transistor Sensors

17 November 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Widespread, persistent, and toxic per- and polyfluoroalkyl substances (PFAS) pose a major threat to both water systems and human health. Current PFAS detection methods are relatively expensive, slow, and complex. To combat PFAS contamination and meet increasingly stringent regulations of PFAS in drinking water, the development of highly sensitive and selective PFAS sensing techniques is urgently needed. Herein, we present an ultrasensitive sensing platform for perfluorooctane sulfonic acid (PFOS) detection in tap water with a reporting limit (~250 ppq) lower than the maximum contaminant level (4 ppt) set by the U.S. Environmental Protection Agency, using remote gate field-effect transistor (RGFET) sensors featuring β-cyclodextrin (β-CD)-modified reduced graphene oxide as the sensing membrane. The sensor exhibits excellent selectivity against common inorganic ions (e.g., Na+, K+, Ca2+, Cl-, HPO42-, SO42- ) and select organic pollutants (e.g., trichloroacetic acid) in tap water. Importantly, the reversible and rapid response (< 2 min) indicates the potential of RGFET for continuous inline monitoring of PFAS. Quartz crystal microbalance results emphasize the important roles of both analyte adsorption and charge properties of analytes and buffers in generating sensing signals. The binding nature between β-CD probe and PFOS or interferent molecules, as well as the spatially resolved selectivity revealed by molecular dynamics simulations, suggest rational probe engineering strategies for future selective capture probe design.

Keywords

PFAS Detection
Water Contaminants
Field-Effect Transistor (FET) Sensors
Interaction Study
Cyclodextrins

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