Highly sensitive OFET based room temperature operated gas sensors using a thieno[3,2b]thiophene extended phthalocyanine semiconductor

Recep Isci*, Ozgur Yavuz, Sheida Faraji, Dilara Gunturkun, Mehmet Eroglu, Leszek A. Majewski, Ismail Yilmaz*, Turan Ozturk*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Over the past decades, organic field-effect transistor (OFET) gas sensors have maintained a rapid development. However, the majority of OFET gas sensors show insufficient detection capability towards oxidizing and hazardous gases such as nitrogen dioxide (NO2) and sulfide dioxide (SO2). In this report, a sustainable approach toward the fabrication of OFET gas sensors, consisting of a thieno[3,2-b]thiophene (TT) and phthalocyanine (Pc) based electron rich structure (TT-Pc) for the detection of both nitrogen dioxide (NO2) and sulfide dioxide (SO2) is disclosed for the first time. Khaya gum (KG), a natural, biodegradable biopolymer is used as the gate dielectric in these OFET-based sensors. Thin film properties and surface morphology of TT-Pc were investigated by UV-Vis, SEM, AFM and contact angle measurements, which indicated a uniform and smooth film formation. The UV-Vis properties were supported by computational chemistry, performed using density functional theory (DFT) for optimizing geometry and absorption of TT-Pc models. Sensitive and selective responses of 90% and 60% were obtained from TT-Pc OFET-based sensors upon exposure to 20 ppm of NO2 and SO2, respectively, under ambient conditions. One of the lowest limits of detection of B165 ppb was achieved for both NO2 and SO2 using a solution-processed TT-Pc sensor with a natural, biodegradable dielectric biopolymer. The sensors showed excellent long-term environmental and operational stability with only a 7% reduction of the sensor’s initial response (%) upon exposure to NO2 and SO2 over nine months of operation in air.

Original languageEnglish
JournalJournal of Materials Chemistry C
DOIs
Publication statusAccepted/In press - 2024

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry 2024.

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