Engineering Nickel(II) Porphyrin-Conjugated Polymers with Different Aryl -Substituents for n-Type and p-Type Ammonia Sensors.

Conjugated polymers have revolutionized the field of conductometric gas sensors for sensing toxic gases arising from the fast urbanization and industrialization. In this work, we report the synthesis of a series of 5,15-diaryl Ni(II) porphyrin-conjugated polymers () and their integration as the top layer on an octafluorinated copper phthalocyanine () sublayer to construct bilayer heterojunction (BLH) devices for ammonia sensing. For the first time, we report the pioneering demonstration of polarity engineering within a BLH device by manipulating the -substituent of the 5,15-diaryl Ni(II) porphyrin-conjugated polymer constituting the top layer of the BLH device. The BLH devices prepared from the 5,15-diaryl Ni(II) porphyrin-conjugated polymer bearing electron-donating -substituents as the top layer exhibit a p-type behavior, whereas an n-type behavior is observed for the BLH devices prepared from the 5,15-diaryl Ni(II) porphyrin-conjugated polymer bearing electron-withdrawing -substituents. Laser desorption ionization high-resolution mass spectrometry, UV/vis/NIR, and X-ray photoelectron spectroscopy studies provide evidence of a decrease in intramolecular dehydrogenative coupling in bearing electron-withdrawing -substituents, resulting in low electrical conductivity of the thin films. Density functional theory calculations reveal noninvolvement of electron-withdrawing -substituents toward π-delocalization in the fused Ni(II) porphyrin tapes. Interestingly, all the / BLH devices exhibit remarkable sensing response toward NH. Among all the devices, displays the highest sensitivity of -1.17% ppm for NH, whereas and exhibit the best limit of detection for NH, below 200 ppb. In addition, shows short response and recovery times of 13 and 255 s, respectively, making this device highly suitable for deployment in emergency services.