Principal goals in organic thin-film transistor (OTFT) gate dielectric research include achieving: (i) low gate leakage currents and good chemical/thermal stability, (ii) minimized interface trap state densities to maximize charge transport efficiency, (iii) compatibility with both p- and n- channel organic semiconductors, (iv) enhanced capacitance to lower OTFT operating voltages, and (v) efficient fabrication via solution-phase processing methods. In this Review, we focus on a prominent class of alternative gate dielectric materials: self-assembled monolayers (SAMs) and multilayers (SAMTs) of organic molecules having good insulating properties and large capacitance values, requisite properties for addressing these challenges. We first describe the formation and properties of SAMs on various surfaces (metals and oxides), followed by a discussion of fundamental factors governing charge transport through SAMs. The last section focuses on the roles that SAMs and SAMTs play in OTFTs, such as surface treatments, gate dielectrics, and finally as the semiconductor layer in ultra-thin OTFTs.

Molecular self-assembled monolayers and multilayers for organic and unconventional inorganic thin-film transistor applications

In a continuation of previous studies, the wetting properties of the hydrophobic diureapropyltriethoxysilane [bis(aminopropyl)-terminated polydimethylsiloxane (1000)] (PDMSU) sol-gel hybrid, which forms washing-resistant water-repellent finishes on cotton fabrics, were further investigated. The addition of 1H,1H,2H,2H-perfluorooctyltriethoxysilane (PFOTES) to PDMSU resulted in a highly apolar low-energy surface on aluminum with gammaStotal equal to 14.5 mJ/m2 and a DetlaGiwi value of -82 mJ/m2. Mixed PFOTES-PDMSU finishes applied on cotton fabrics increased the water contact angles (thetaw) from approximately 130 degrees (PDMSU) to 147 degrees, also imparting oleophobicity (thetadiiodomethane=130 degrees, thetan-hexadecane=120 degrees) to the finished cotton fabrics. Washing caused breakage of the coating's integrity as established from SEM, which was attributed to the partial removal of PFOTES from the composite films, also shown by subtractive IR attenuated total reflectance (ATR) and XPS spectral measurements made on washed and unwashed fabrics. The antibacterial properties of the PFOTES-PDMSU-finished fabrics were assessed with the transfer method (EN ISO 20743:2007), revealing that the reduction of Escherichia coli bacteria on unwashed cotton fabrics was nearly 100%. Moreover, for washed (10 times) cotton fabrics a much higher bacterial reduction was noted for the PFOTES-PDMSU finishes (60.6+/-10.8%), surpassing PDMSU (30.4+/-6.1%) and commercial fluoroalkoxysilane (FAS) (21.9+/-5.7%) finishes. The structure of PFOTES-PDMSU gels, xerogels, and the corresponding coatings was investigated by analyzing the 29Si NMR and IR ATR spectra and comparing them with the spectra of PFOTES and octameric (T8) PFOTES based polyhedra. The results revealed the tendency of PFOTES to condense in octameric silsesquioxane polyhedra (T8), coexisting in the PDMSU sol-gel network with cyclic tetramers (T4(OH)4) and open cube-like species (T7(OH)3). The presence of -OH-functionalized PFOTES silsesquioxanes, established even in coatings heat-treated at 140 degrees C (15 min), also explained the excellent washing fastness of PFOTES finishes on cotton fabrics. The regenerative nature of the water- and oil-repellent properties of washed PFOTES-PDMSU-finished cotton fabrics was attributed to the surface mobility of the T8 PFOTES based polyhedra, ousted from the coating interior during consecutive washings.

Structural Properties and Antibacterial Effects of Hydrophobic and Oleophobic Sol-Gel Coatings for Cotton Fabrics

Multifunctional, water and oil repellent and antimicrobial finishes for cotton fibres were prepared from a commercially available fluoroalkylfunctional water-born siloxane (FAS) (Degussa), nanosized silver (Ag) (CHT) and a reactive organic–inorganic binder (RB) (CHT). Two different application procedures were used: firstly, one stage treatment of cotton fabric samples by FAS sol (i), as well as by a sol mixture constituted from all three precursors (Ag–RB–FAS, procedure 1S) (ii), and secondly, two stage treatment of cotton by Ag–RB sol and than by FAS sol (Ag–RB + FAS, procedure 2S) (iii). The hydrophobic and oleophobic properties of cotton fabrics treated by procedures (i)–(iii) before and after consecutive (up to 10) washings were established from contact angle measurements (water, diiodomethane and n-hexadecane) and correlated with infrared and XPS spectroscopic measurements. The results revealed that even after 10 washing cycles cotton treated with Ag–RB + FAS (2S) retained an oleophobicity similar to that of the FAS treated cotton, while the Ag–RB–FAS (1S) cotton fibres exhibited a loss of oleophobicity already after the second washing, even though fluorine and C–F vibrational bands were detected in the corresponding XPS and IR spectra. The antibacterial activity of cotton treated by procedures (i)–(iii) was tested by its reduction of the bacteria Escherichia coli and Staphylococcus aureus following the AATCC 100-1999 standard method and EN ISO 20743:2007 transfer method. The reduction in growth of both bacteria was nearly complete for the unwashed Ag–RB and Ag–RB–FAS (S1), but for the unwashed Ag–RB + FAS (S2) treated cotton no reduction of S. aureus and 43.5 ± 6.9% reduction of E. coli was noted. After the first washing, the latter two finishes exhibited nearly a complete reduction of E. coli but for the Ag–RB treated cotton the reduction dropped to 88.9 ± 3.4. None of the finishes retained antibacterial properties after 10 repetitive washings. The beneficial and long-lasting low surface energy effect of FAS finishes in the absence of Ag nanoparticles, which led to the “passive” antibacterial properties of FAS treated cotton fabrics, was established by applying the EN ISO 20743:2007 transfer method. The results revealed a reduction in bacteria of about 21.9 ± 5.7% (FAS), 13.1 ± 4.8% (Ag–RB–FAS (S1)) and 41.5 ± 3.7% (Ag–Rb + FAS (S2)), while no reduction of the growth of bacteria was observed for cotton treated with Ag nanoparticles after 10 repetitive washings. The physical properties (bending rigidity, breaking strength, air permeability) of finished cotton samples were determined, and showed increased fabric softness and flexibility as compared to the Ag–RB treated cotton, but a slight decrease of breaking strength in the warp and weft directions, while air permeability decreased for all type of finishes.

Sol–gel coating of cellulose fibres with antimicrobial and repellent properties

With the advances of organic field-effect transistors (OFETs), the interface between semiconductors and dielectrics has received much attention due to its dramatic effects on the morphology and charge-transport of organic semiconductors in OFETs. The purpose of this review is to give an overview of the recent progress in the engineering of the dielectric–semiconductor interface in OFETs. The interface-dependent performances of OFETs are reviewed, and interfacial control methods are especially dealt with an aim to solve interfacial effects. Finally, novel applications of the dielectric–semiconductor interface for achieving multifunctions are summarized to offer a clear map of interface engineering in OFETs.

Engineering of the dielectric–semiconductor interface in organic field-effect transistors

Self-assembled monolayers (SAMs) are rapidly becoming an essential part of organic electronics such as light emitting diodes (LEDs), organic field-effect transistors (OFETs), and complementary circuits, where they are employed to control the morphology and energetics of the interfaces. This review will focus on interface engineering and its influence on such devices. We will describe the growth of SAMs of organic molecules on various surfaces of interest for this purpose (mainly metals and oxides). For the growth of SAMs on metal electrodes, the most common approach makes use of thiols to modify the metal surface, but the preparation of SAMs on dielectrics requires other reactive groups such as carboxylic or phosphonic acids. We review also the control of the interfacial properties by appropriate molecular design of the SAMs and their effect on device performance. SAMs can modify the morphology of the organic semiconductor, the dielectric properties of the insulator, the electronic states at the dielectric interface and the level alignment at the electrode interfaces. All these factors can influence current transport mainly by modifying the charge mobility, the contact resistance and the trap density at the interfaces.

Surface engineering for high performance organic electronic devices: the chemical approach

Formation of stable and hydrophobic self-assembled monolayers (SAMs) on an oxidized copper (Cu) surface has been accomplished via reaction with 1H,1H,2H,2H-perfluorodecyldimethylchlorosilane (PFMS). The perfluoroalkyl SAMs showed sessile drop static contact angles of more than 125° for pure water and stability against exposure to boiling water, boiling nitric acid solution, and warm sodium hydroxide solution for up to 30 min. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared reflection/absorption spectroscopy (FT-IRRAS) data reveal a coordination of the PFMS silicon (Si) atom with a cuprate (CuO) molecule present on the oxidized copper substrate. The data give good evidence that the stability of the SAM film on the PFMS-modified oxidized Cu surface is largely due to the formation of a siloxy−copper (−Si−O−Cu−) bond via a condensation reaction between silanol (−Si−OH) and copper hydroxide (−CuOH). The extremely hydrophobic and stable SAMs on oxidized Cu could have useful applications in...

J. A. DeRose

Papers

Stable Perfluorosilane Self-Assembled Monolayers on Copper Oxide Surfaces: Evidence of Siloxy−Copper Bond Formation