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OFETs

Because most of the OFETs reported until now were grown on silicon wafers, the deposition of the semiconductor is the determining step of their fabrication. De-... [Pg.257]

Figure 14-12. Various types of OFETs. (a) Inverted coplanar on a highly doped Si wafer, (b) inverted coplanar on a neutral substrate, (c) inverted staggered oil a neutral substrate, (d) inverted staggered using the dielectric layer as the substrate. Figure 14-12. Various types of OFETs. (a) Inverted coplanar on a highly doped Si wafer, (b) inverted coplanar on a neutral substrate, (c) inverted staggered oil a neutral substrate, (d) inverted staggered using the dielectric layer as the substrate.
OFETs constructed on a silicon wafer do not lake advantage of one of the main interest of organic materials, namely the possibility of building electronic devices on plastic substrates. A second important drawback of the silicon-based structure is the difficulty to individually address the gale of transistors built on the same wafer, which would prevent the achievement of integrated circuits. [Pg.258]

More recently. Gamier and coworkers used a printing technique to make OFETs on polymeric substrates [61]. Although printable field-effect transistors based on inorganic semiconductors have been reported as early as 1967 ]62], they did not come to any commercial development. We note, however, that in Gar-nier s device only the electrodes were actually printed. [Pg.258]

Figure 14-13. Evolution of the field-effect mobility of OFETs for five organic materials polythio-phenc (PT) and its derivatives, qualerthiophcne (4T), scxithio-phenc (6T), dihcxyl-sexithiophene (DH6T). and pcntaecnc. Figure 14-13. Evolution of the field-effect mobility of OFETs for five organic materials polythio-phenc (PT) and its derivatives, qualerthiophcne (4T), scxithio-phenc (6T), dihcxyl-sexithiophene (DH6T). and pcntaecnc.
Tablc 14-3. Performance of OFETs made with n-lypc organic semiconductors. [Pg.262]

The development of microelectronics cannot be envisaged without a comprehensive modeling of the devices. The modeling of OFETs is currently hampered by several features. First, charge transport in organic semiconductors is still not completely understood. The situation is clear at both ends of the scale. In high mobility materials (//>IOcnr V-1 s l), transport occurs within delocalized levels when temperature... [Pg.263]

Figure 14-22. Variation of the square root of the saturation current as a function of the gate voltage for a typical lightly doped DH6T OFET. Figure 14-22. Variation of the square root of the saturation current as a function of the gate voltage for a typical lightly doped DH6T OFET.
We Finally note that the MTR model is a priori more appropriate to disordered materials. It is not expected to give good results with single crystal OFET, especially when the mobility becomes temperature-independent (see Section 14.6.1.2). However, it has recently been invoked in the case of poly thiophene [112], the mobility of which is also thermally activated. [Pg.265]

Figure 14-27. Drain current-voltage charaeieristics of a doped DH6T OFET sliowiug both accumulation (V cO) and depletion (Fx>0) regimes. Figure 14-27. Drain current-voltage charaeieristics of a doped DH6T OFET sliowiug both accumulation (V cO) and depletion (Fx>0) regimes.
Table 14-2. Performance of pcnlacene based OFETs. Mobility in cm2 V 1 s substrate temperature in °C. RT room temperature. Table 14-2. Performance of pcnlacene based OFETs. Mobility in cm2 V 1 s substrate temperature in °C. RT room temperature.
More recently, OFETs were made with a dimer of another condensed molecule. dithieno[3,2-/j 2, 3 -c/ lhiophene 100, which presents a very similar structure lo that of benzodithiophene, except that the central benzene ring is changed lo a... [Pg.573]

This section is divided in two parts. In the first one, we review the studies on the transport mechanism in materials used in OFETs, whereby temperature-depen-dent measurements are a very powerful tool. The study of the gate bias dependence has also been used by researchers. In the second part, we present the few analytical models of the organic FETs that have been developed until now. [Pg.575]

As all measurements were performed in air, il is mosl probably due lo oxygen doping, a feature that lias been already noticed in oligolhiophene 1101 and poly-thiophene 11281 OFETs. [Pg.579]

As a class of n-type organic semiconductors, PBI derivatives have received considerable attention for a variety of applications [312, 313], for example, for organic or polymer light-emitting diodes (OLEDs and PLEDs) [314, 315], thin-film organic field-effect transistors (OFETs) [316, 317], solar cells [318, 319], and liquid crystals [320]. They are also interesting candidates for single-molecule device applications, such as sensors [321], molecular wires [322], or transistors [141]. [Pg.166]

If amorphous Si TFTs and OFETs are adequate only for lower performance, lower cost applications, what are the options for more advanced applications To achieve the higher performance that is desired while keeping process technology consistent with the goals of macroelectronics, several different fabrica-... [Pg.14]

But, it is substantially better than the tens of kilohertz that classic amorphous silicon or OFETs can achieve. It is also in frequency ranges of interest for many mobile communication systems and radar detection bands and, therefore, would provide sufficient capability for a range of RF opportunities. [Pg.17]


See other pages where OFETs is mentioned: [Pg.218]    [Pg.231]    [Pg.12]    [Pg.244]    [Pg.252]    [Pg.257]    [Pg.258]    [Pg.258]    [Pg.259]    [Pg.260]    [Pg.261]    [Pg.261]    [Pg.262]    [Pg.267]    [Pg.267]    [Pg.268]    [Pg.565]    [Pg.569]    [Pg.570]    [Pg.570]    [Pg.570]    [Pg.573]    [Pg.573]    [Pg.574]    [Pg.575]    [Pg.575]    [Pg.578]    [Pg.578]    [Pg.579]    [Pg.197]    [Pg.197]    [Pg.557]    [Pg.458]    [Pg.13]   
See also in sourсe #XX -- [ Pg.86 , Pg.104 , Pg.173 ]

See also in sourсe #XX -- [ Pg.186 , Pg.216 ]

See also in sourсe #XX -- [ Pg.2 , Pg.92 , Pg.155 , Pg.189 , Pg.213 , Pg.218 , Pg.302 ]




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Access resistance, OFET

Accumulation regime, OFETs

Advanced OFET fabrication

Alternative OFET designs

BDT Based Polymers in OFET Application

Band OFETs

Basic OFET fabrication

Basic OFET structure and operation

Between Metal Diffusion and Device Properties of OFETs

Blend film OFETs

Bonding What can be Learned for OFETs

Bottom-gate OFET structure

Building OFETs

Conducting OFETs

Conduction OFETs

Conjugated OFETs

Contact resistance values, OFET

Contacts OFETs

Crystallization rate, OFET

Current OFETs

Depletion OFETs

Electrochemical OFETs

Electron-accumulation mode, OFET

Evaporation OFETs

Fermi OFETs

Ferroelectric OFET

Fullerenes OFETs

Heterojunctions OFETs

Hole-accumulation mode, OFET

Junctions OFETs

Layers OFETs

Materials OFETs

OFET Based on a Modified PPV and with Silanised Gate Oxide

OFET Device Fabrication

OFET Performance Characteristics

OFET Studies

OFET materials

OFET on Foil Substrates

OFETs CMOS inverters

OFETs ambipolar

OFETs field-effect mobility

OFETs models

OFETs short-channel

OFETs transistors

OFETs unipolar

Ohmic contacts, OFETs

Optimised Sub-micron OFETs

Organic field effect transistors OFET electrodes

Organic field effect transistors OFET)

Organic field-effect transistors (OFETs

Organic semiconductor devices OFETs)

Organic semiconductor materials for OFETs

Pentacene OFETs

Pentacene OFETs With Bottom Contacts

Polymer semiconductor development OFETs

Sensing Mechanisms and OFET Models

Short Channel OFET Based on P3HT

Single-Crystal OFETs Prepared on Well-Ordered Sapphire Substrates

Single-crystal organic field-effect transistors OFETs

Small OFETs

Solution OFETs

Spectroscopic Characterisation of Interfaces and Dielectric Layers for OFET Devices

Structure What can be Learned for OFETs

The Present Micro-OFET Concept

Thin OFETs

Top-Contacted Pentacene OFETs

Unipolar Films for OFETs

Voltage drops, OFETs

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