Affiliation:
1. Department of Chemical Engineering and Waterloo Institute of Nanotechnology, (WIN) University of Waterloo 200 University Ave West Waterloo N2L 3G1 Canada
2. Security and Disruptive Technologies National Research Council Canada 1200 Montreal Road Ottawa Ontario K1A 0R6 Canada
3. College of Chemistry Chemical Engineering and Materials Science Soochow University Suzhou 215123 P. R. China
Abstract
AbstractThe study has developed two hemi‐isoindigo (HID)‐based polymers for printed flexible resistor‐type nitrogen oxide (NO2) sensors: poly[2‐ethylhexyl 3‐((3′“,4′‐bis(dodecyloxy)‐3,4‐dimethoxy‐[2,2′:5′,2′”‐terthiophen]‐5‐yl)methylene)‐2‐oxoindoline‐1‐carboxylate] (P1) and poly[2‐ethylhexyl 2‐oxo‐3‐((3,3′“,4,4′‐tetrakis(dodecyloxy)‐[2,2′:5′,2′”‐terthiophen]‐5‐yl)methylene)indoline‐1‐carboxylate] (P2). These polymers feature thermally removable carbamate side chains on the HID units, providing solubility and creating molecular cavities after thermal annealing. These cavities enhance NO2 diffusion, and the liberated unsubstituted amide ─C(═O)NH─ groups readily form robust double hydrogen bonds (DHB), as demonstrated by computer simulations. Furthermore, both polymers possess elevated highest occupied molecular orbital (HOMO) energy levels of −4.74 and −4.77 eV, making them highly susceptible to p‐doping by NO2. Gas sensors fabricated from P1 and P2 films, anneal under optimized conditions to partially remove carbamate side chains, exhibit remarkable sensitivities of +1400% ppm−1 and +3844% ppm−1, and low detection limit (LOD) values of 514 ppb and 38.9 ppb toward NO2, respectively. These sensors also demonstrate excellent selectivity for NO2 over other gases.
Funder
Natural Sciences and Engineering Research Council of Canada
Cited by
2 articles.
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