Non-faradaic capacitive cation sensing under flow

Sophie C. Patrick

doi:10.1039/d4sc05271d

2024-01-01

DOI：10.1039/d4sc05271d

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The ability to continually monitor target ion species in real-time is a highly sought-after endeavour in the field of host-guest chemistry, given its direct pertinence to medical and environmental applications. Developing methodologies which support sensitive and continuous ion sensing in aqueous media, however, remains a challenge. Herein, we present a versatile and facile, proof-of-concept electrochemical sensing methodology based on non-faradaic capacitance, which can be operated continuously with high temporal resolution (approximate to 1.4 s), in conjunction with custom-designed integrated microfluidics. The potential of this method is demonstrated for cation sensing at a chemically simple benzo-15-crown-5-based molecular film (B15C5SAM) as a representative redox-inactive, receptive interface. Detection limits as low as 4 mu M are obtained for Na+ by these entirely reagentless analyses, and are additionally characterised by exceptional baseline stabilities that are able to support continuous sensing over multiple days. The platform performs well in artificial sweat across physiologically relevant spans of sodium concentration, and provides meaningful dose-dependent responses in freshwater samples. Finally, the high assay temporal resolution affords an ability to resolve both the kinetics of binding (association/dissociation) and notably characteristic fingerprints for different alkali metals which may be diagnostic of different interfacial ion binding modes. The ability to continually monitor target ion species in real-time is a highly sought-after endeavour in the field of host-guest chemistry, given its direct pertinence to medical and environmental applications.

Keyword:

SELF-ASSEMBLED MONOLAYERS

CROWN-ETHERS

ION

COMPLEXES

RECOGNITION

DERIVATIVES

15-CROWN-5

ELECTRODE

SENSOR

AMIDE