- Title
- Fabrication and characterisation of organic thin-film transistors for sensing applications
- Creator
- Elkington, Daniel
- Relation
- University of Newcastle Research Higher Degree Thesis
- Resource Type
- thesis
- Date
- 2013
- Description
- Research Doctorate - Doctor of Philosophy (PhD)
- Description
- Organic thin-film transistors (OTFTs) are a family of devices in the area of organic electronics which are generating a large amount of interest due to the wide variety of potential applications for transistors which have all the benefits associated with using organic materials. These benefits include low-temperature and low-power fabrication possibilities, the use of flexible substrates and the low cost of materials. Previous literature on OTFTs comprising poly-3-hexylthiophene (P3HT) semiconductor layers, poly(4-vinylphenol) (PVP) dielectric layers and poly(3,4-ethylenedioxy-thiophene) poly(styrenesulfonate) (PEDOT:PSS) gate electrodes have reported on their relatively high performance at low operating voltages. However, there still remains the potential for further investigations to discover more about the nature of the current modulation mechanism(s) in these types of OTFTs. Several experiments were carried out to probe their operation mechanisms and determine their suitability for applications such as biosensors. The results of many of these experiments indicated that ions donated from the acidic PEDOT:PSS gate material as well as those liberated from water in air contribute to current modulation by doping and de-doping of the P3HT semiconductor. Poly(vinyl-pyridine) (PVPy) was then introduced as a dielectric material to replace PVP. PVPy contrasts in its chemical properties with PVP: rather than allowing and contributing to the free movement of protons within it as the acidic PVP does, the chemically basic PVPy will tend to bind protons to its pyridal groups, restricting their movement. It was shown that this change in material reduces the off current (IOFF) of the devices (by inhibiting any doping of P3HT which occurs upon PEDOT:PSS deposition), however the on current (ION) was also reduced and thus no real improvement in current modulation ration(ION/IOFF) was achieved. Whilst some aspects of device performance were improved when PVPy was used as the dielectric layer instead of PVP, the current modulation ratio remained low. Subsequent experiments showed that the addition of a dopant salt (LiClO4) to the PVPy layer can substantially increase the current modulation ratio of the OTFTs. In fact, it was demonstrated that the current modulation ratio can be controlled by varying the amount of salt added to each device. The nature of the drain current (ID) response to changes in gate voltage (VGS) in the time domain indicates that electrochemical doping, and not an electrostatic mechanism, is the nature of the mechanism causing current modulation (similar to the previous un-doped devices). NaClO4 was also trialled as a candidate for the dopant salt and, despite Na+ being larger than Li+, it appeared to move more freely within the device which is consistent with a hydration sphere model and therefore supports the idea that the dielectric layer is moisture-rich when operating in air. Finally, OTFTs incorporating the enzyme glucose oxidase (GOX) were fabricated for use as glucose sensors. GOX selectively oxidises glucose and it was hypothesised that the ions liberated in this oxidation reaction could contribute to the ionic processes which contribute to current modulation in the devices and therefore a relationship between the quantity of glucose exposed to the device and the ID level could be established. The results presented here show that devices with embedded GOX do indeed show a relationship between glucose concentration and ID when an analyte solution is deposited onto the device.
- Subject
- organic transistors; organic electronics; sensors; OTFT
- Identifier
- http://hdl.handle.net/1959.13/940864
- Identifier
- uon:13116
- Rights
- Copyright 2013 Daniel Elkington
- Language
- eng
- Full Text
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View Details Download | ATTACHMENT02 | Thesis | 6 MB | Adobe Acrobat PDF | View Details Download |