JOURNAL ARTICLE
Chemi-Resistive Sensor for Ammonia Using Inkjet Printing of GO/PEDOT:PSS Composite at Room Temperature.
Published In: Nano Life, 2025, v. 15, n. 1. P. 1 1 of 3
Database: Academic Search Ultimate 2 of 3
Authored By: Chhapia, Pratik; Patel, Harshad 3 of 3
Abstract
This study describes an easy and cheap inkjet printing method for producing a paper-based gas sensor consisting of a composite film made of graphene oxide and poly(3,4-ethylenedioxythiophene) and poly(styrenesulfonate) (PEDOT:PSS). A glossy paper substrate is an inkjet printed with ink made by dispersing graphene oxide in a PEDOT:PSS conducting polymer solution to test its ability to detect ammonia ( NH 3) at ambient temperature. The presence of few-layer graphene oxide in the PEDOT:PSS copolymer and the existence of π – π interactions between graphene oxide and PEDOT:PSS are confirmed by Fourier transform infrared spectroscopy, UV–Visible spectrophotometer, and X-ray diffraction. In a small concentration range of 1–100 ppm at ambient temperature, the ink-jet printed graphene oxide-PEDOT:PSS gas sensor displays strong responsiveness and good selectivity to NH3. The study found that NH 4 is a strong donor in the ammonia gas produced by a bubble system of ammonia water, with NH 4 molecules being ideal candidates for molecular doping of graphene. The H 2 O molecule can facilitate quick desorption by converting NH 3 to NH 4 . The interaction between graphene oxide and NH 3 molecules is weak. The attained gas-sensing performance may be attributed to the increased specific surface area of graphene oxide and enhanced interactions between the sensing film and NH 3 molecules via π and lone pair electron network. The NH 3 -sensing mechanisms of the flexible printed gas sensor are based on the competitive interaction of ammonia on the sensor, adsorption and dissociate ionization on the sensor surface. [ABSTRACT FROM AUTHOR]
Additional Information
- Source:Nano Life. 2025/02, Vol. 15, Issue 1, p1
- Document Type:Article
- Subject Area:Science
- Publication Date:2025
- ISSN:1793-9844
- DOI:10.1142/S1793984424500107
- Accession Number:179044323
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