Papertronics: Integrating Electronics and Microfluidics on Paper for Sustainable Electroanalysis

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

Abstract

The widespread use of non-renewable materials in point-of-care (PoC) electroanalysis, such as disposable test strips with electronic meters, has inadvertently contributed to electronic waste. Paper, traditionally used as a passive substrate, offers a renewable alternative but faces limitations in direct conversion into conductive electronic components, hindering its adoption for on-site analysis. Here, we present the development of papertronics, integrating conductive electronic components and microfluidics on a single sheet of paper for sustainable electroanalysis. Using a flame retardant and laser treatment, we enable a direct conversion of cellulose paper into laser-induced graphite (PLIG). By optimizing laser parameters (e.g., laser power, scan speed and defocus/focus), the physicochemical properties of the PLIG are tailored. Microfluidic channels are patterned with sub-millimetre resolution via hot-pressing hydrophobic parafilm into paper at a relatively low temperature of 60 °C for 15 seconds. This process facilitates a seamless integration of paper-based electronic components with microfluidics. Demonstrative applications in pH sensing showed a sensitivity of -40.3 mV pH-1, and lactate biosensing achieved a sensitivity of 0.92 μA mM-1. This study establishes a foundation for cost-effective, environmentally friendly electroanalytical platforms with broad implications in biomedical diagnostics and environmental monitoring.

Keywords

papertronics
paper
laser
microfluidics
sustainability
electroanalysis

Supplementary materials

Title
Description
Actions
Title
Supporting information
Description
Supporting optical images, XPS, FTIR, SEM, wettability measurements.
Actions

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.