Thin-film transistors for chemical sensor applications
A chemical sensor is disclosed. The chemical sensor is an electronic device including in specific embodiments a first transistor and a second transistor. The first transistor includes a semiconducting layer made of a first semiconductor and carbon nanotubes. The second transistor includes a semiconducting layer made of a second semiconductor, and does not contain carbon nanotubes. The two transistors vary in their response to chemical compounds, and the differing response can be used to determine the identity of certain chemical compounds. The chemical sensor can be useful as a disposable sensor for explosive compounds such as trinitrotoluene (TNT). The electronic device is used in conjunction with an analyzer that processes information generated by the electronic device.
1. An electronic device for determining the identity of a chemical compound, the device comprising a first transistor and a second transistor;
wherein the first transistor comprises a first gate electrode, a first source electrode, a first drain electrode, and a first semiconducting layer, the first semiconducting layer comprising a first semiconductor polythiophene and carbon nanotubes;
wherein the second transistor comprises a second gate electrode, a second source electrode, a second drain electrode, and a second semiconducting layer, wherein the second semiconducting layer comprises a second semiconductor polythiophene and does not contain carbon nanotubes;
wherein the first transistor and the second transistor, when exposed to the chemical compound, produce a change in charge carrier mobility which is indicative of the chemical compound, and
the ratio of the change in charge carrier mobility of the first transistor and the second transistor confirms the identity of the chemical compound.
2. The electronic device of claim 1 , wherein the chemical compound is selected from the group consisting of hydrocarbons containing one or more nitro groups, chlorinated hydrocarbons, alcohols, and aromatic hydrocarbons.
3. The electronic device of claim 1 , wherein the first semiconductor polythiophene and the second semiconductor polythiophene each have the structure of Formula (II):
wherein m is from 2 to about 2,500.
4. The electronic device of claim 1 , wherein the carbon nanotubes are surface-modified carbon nanotubes.
5. The electronic device of claim 1 , wherein the carbon nanotubes comprise from about 1 wt % to about 50 wt % of the first semiconducting layer, based on the total weight of the first semiconductor and the carbon nanotubes.
6. The electronic device of claim 1 , wherein the first semiconductor polythiophene and the second semiconductor polythiophene independently have a structure of Formula (I):
wherein A is a divalent linkage; wherein each R is independently selected from hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, alkoxy, substituted alkoxy, a heteroatom-containing group, halogen, —CN, or —NO 2 ; and wherein n is from 2 to about 5,000.