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/content/aip/journal/apl/106/26/10.1063/1.4923397
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14.See supplementary material at http://dx.doi.org/10.1063/1.4923397 for experimental details and auxiliary experiments.[Supplementary Material]
http://aip.metastore.ingenta.com/content/aip/journal/apl/106/26/10.1063/1.4923397
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/content/aip/journal/apl/106/26/10.1063/1.4923397
2015-06-29
2016-09-26

Abstract

The effect of device architecture upon the response of printable enzymatic glucose sensors based on poly(3-hexythiophene) (P3HT) organic thin film transistors is presented. The change in drain current is used as the basis for glucose detection and we show that significant improvements in drain current response time can be achieved by modifying the design of the sensor structure. In particular, we show that eliminating the dielectric layer and reducing the thickness of the active layer reduce the device response time considerably. The results are in good agreement with a diffusion based model of device operation, where an initial rapid dedoping process is followed by a slower doping of the P3HT layer from protons that are enzymatically generated by glucose oxidase (GOX) at the Nafion gate electrode. The fitted diffusion data are consistent with a P3HT doping region that is close to the source-drain electrodes rather than located at the P3HT:[Nafion:GOX] interface. Finally, we demonstrate that further improvements in sensor structure and morphology can be achieved by inkjet-printing the GOX layer, offering a pathway to low-cost printed biosensors for the detection of glucose in saliva.

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