OFETS HAVING ORGANIC SEMICONDUCTOR LAYER WITH HIGH CARRIER MOBILITY AND IN SITU ISOLATION
An organic field effect transistor includes a channel structure defining an active area located between a source and a drain. The channel structure includes a photoalignment layer and an organic semiconductor layer disposed directly over the photoalignment layer. The photoalignment layer is configured to influence an orientation of molecules within the organic semiconductor layer and hence impact the mobility of charge carriers both within the active area and adjacent to the active area.
1 . An organic field effect transistor comprising:
a channel structure defining an active area located between a source and a drain, the channel structure comprising a photoalignment layer and an organic semiconductor layer disposed directly over the photoalignment layer.
2 . The organic field effect transistor of claim 1 , wherein the photoalignment layer comprises a material selected from the group consisting of azo-compounds, polyimides, polysilanes, polystyrenes, polyesters, cinnamates, coumarins, chalconyls, tetrahydrophthalimides, and maleimides.
3 . The organic field effect transistor of claim 1 , wherein the photoalignment layer is configured to influence an orientation of molecules within the organic semiconductor layer.
4 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer comprises a polycrystalline layer or a single crystal layer.
5 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer comprises a polycyclic aromatic hydrocarbon.
6 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer comprises a molecule selected from the group consisting of naphthalene, anthracene, tetracene, pentacene, pyrene, polycene, fluoranthene, benzophenone, benzochromene, benzil, benzimidazole, benzene, hexachlorobenzene, nitropyridine-N-oxide, benzene-1, 4-dicarboxylic acid, diphenylacetylene, N-(4-nitrophenyl)-(s)-prolinal, 4,5-dicyanoimidazole, benzodithiophene, cyanopyridine, thienothiophene, stilbene, and azobenzene.
7 . The organic field effect transistor of claim 1 , further comprising a gate structure located proximate to the channel structure, the gate structure configured to control the conductivity of the channel structure within the active area.
8 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer is characterized by a charge carrier mobility of at least approximately 0.01 cm 2 V −1 s −1 within the active area along a direction between the source and the drain.
9 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer is characterized by a charge carrier mobility of at least approximately 1 cm 2 V −1 s −1 within the active area along a direction between the source and the drain.
10 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer comprises an isolation region adjacent to the active area.
11 . The organic field effect transistor of claim 1 , wherein the organic semiconductor layer comprises an amorphous layer within the isolation region.
12 . A method comprising:
forming a photoalignment layer;
illuminating the photoalignment layer with polarized light to form an oriented photoalignment layer; and
forming an organic semiconductor layer directly over the oriented photoalignment layer.
13 . The method of claim 12 , wherein the photoalignment layer comprises a material selected from the group consisting of azo-compounds, polyimides, polysilanes, polystyrenes, polyesters, cinnamates, coumarins, chalconyls, tetrahydrophthalimides, and maleimides.
14 . The method of claim 12 , wherein the organic semiconductor layer comprises a polycyclic aromatic hydrocarbon.
15 . The method of claim 12 , wherein the organic semiconductor layer comprises a molecule selected from the group consisting of naphthalene, anthracene, tetracene, pentacene, pyrene, polycene, fluoranthene, benzophenone, benzochromene, benzil, benzimidazole, benzene, hexachlorobenzene, nitropyridine-N-oxide, benzene-1, 4-dicarboxylic acid, diphenylacetylene, N-(4-nitrophenyl)-(s)-prolinal, 4,5-dicyanoimidazole, benzodithiophene, cyanopyridine, thienothiophene, stilbene, and azobenzene.
16 . The method of claim 12 , further comprising:
forming a source adjacent to a first region of the organic semiconductor layer; and
forming a drain adjacent to a second region of the organic semiconductor layer, wherein a charge carrier mobility of the organic semiconductor layer within an active area between the source and the drain is greater than a charge carrier mobility of the organic semiconductor layer within an isolation region adjacent to the active area.
17 . The method of claim 16 , wherein the photoalignment layer is illuminated with a first polarized light within the active area and the photoalignment layer is illuminated with a second polarized light within the isolation region.
18 . The method of claim 16 , wherein the organic semiconductor layer is characterized by a charge carrier mobility of at least approximately 0.01 cm 2 V −1 s −1 within the active area along a direction between the source and the drain.
19 . An organic field effect transistor comprising a photoalignment layer and an organic semiconductor layer disposed directly over the photoalignment layer, wherein a first region of the organic semiconductor layer is characterized by a first charge carrier mobility and a second region of the organic semiconductor layer is characterized by a second charge carrier mobility.
20 . The organic field effect transistor of claim 19 , wherein the first region is located within an active area between a source and a drain and the second region comprises an isolation region located adjacent to the active area.