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4th EucheMs chemistry congress

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Poster Session 2<br />

s1201<br />

chem. Listy 106, s257–s1425 (2012)<br />

Poster session 2 - solid state <strong>chemistry</strong><br />

P - 0 6 7 7<br />

effeCt of hydroxyL denSity on<br />

CondenSAtion BehAviorS of SeLf-ASSeMBLed<br />

MonoLAyerS And PerforMAnCe of<br />

PentACene-BASe orGAniC thin-fiLM<br />

trAnSiStorS<br />

M. y. Kuo 1 , h. C. tiAo 1<br />

1 National Chi Nan University, Applied Chemistry, Nantou,<br />

Taiwan<br />

A series of self-assembled monolayers (SAMs), comprising<br />

octadecyltrichlorosilane (ODTS), dodecyltrichlorosilane (DDTS),<br />

and hexamethyldisilazane (HMDS), were prepared to examine the<br />

effects of phase states and condensation behaviors of SAMs on<br />

the morphologies and performance of pentacene-based organic<br />

field-effect transistors (OFETs) by means of Fourier Transform<br />

Infrared (FT-IR) spectrometer, atomic force microscope (AFM),<br />

X-ray diffraction (XRD), and semiconductor parameter analyzer.<br />

Experimental results reveal that the treatment of SiO substrates<br />

2<br />

with O plasma (denoted as O -SiO ) and the preparation<br />

2 2 2<br />

temperature of SAMs dramatically influence the morphologies of<br />

SAMs and the performance of corresponding pentacene-based (no<br />

purification) OFETs. When the SAMs were prepared at 30 °C, the<br />

OFET based on ODTS-treated O -SiO substrate had the highest<br />

2 2<br />

hole mobility, reaching as large as 1.15 cm2V-1s-1 , and an on/off<br />

current ratio in excess of 105 ; these values are both much larger<br />

than those of a device based on ODTS-modified SiO substrates<br />

2<br />

without O plasma treatment and O -SiO substrates modified by<br />

2 2 2<br />

ODTS SAMs prepared at other temperatures. OFETs based on<br />

O -SiO substrates that were modified by DDTS and HMDS<br />

2 2<br />

SAMs prepared at 4 °C performed best.<br />

Keywords: Organic field-effect transistors; self-assembled<br />

monolayer; pentacene; O2 plasma; preparing temperature;<br />

4 th <strong>EucheMs</strong> <strong>chemistry</strong> <strong>congress</strong><br />

P - 0 6 7 8<br />

deveLoPMent of wAter-BASed SoL-GeL<br />

CoAtinGS AS AdheSion Pre-treAtMent for<br />

ALuMiniuM SheetS<br />

S. Meyer 1 , u. SChuBert 1<br />

1 Vienna University of Technology, Institute of Materials<br />

Chemistry, Vienna, Austria<br />

Since 2000, as the chromate conversion coatings were<br />

forbidden in the automotive and aircraft sector, much research has<br />

been done to find a follow-up system for corrosion protection of<br />

aluminium. Sol-gel coatings are very promising because the<br />

precursors can be modified easily and the coatings can be tailored<br />

for different requirements.<br />

This work deals with the development of water-based<br />

coatings providing a good pre-treatment for adhesive bonding as<br />

well a good corrosion protection, even after aging under corrosive<br />

conditions.<br />

Based on a coating system which consists of zirconia<br />

nanoparticles embedded in a silica network [1] made of tetraethyl<br />

orthosilicate (TEOS) and glycidoxypropyltrimethoxysilane<br />

(GLYMO), a water-based coating was developed. Furthermore<br />

the replacement of zirconium by titanium was tested. This new<br />

system was varied with regard to the aging time of the sol, ratio<br />

of transition metal precursor and water proportion. The suitability<br />

as adhesion pre-treatment was tested by tensile shear strength<br />

measurements. Additionally, the aging resistance was investigated<br />

by storing the bonded specimens in a salt spray chamber for<br />

480 hours and testing them after this treatment. Morphological<br />

characterization was done by SEM and the composition was<br />

investigated by XPS.<br />

references:<br />

1. M.L. Zheludkevich, R. Serra, M.F. Montemor, I.M. Miranda<br />

Salvado, M.G.S. Ferreira Surface and Coatings Technology<br />

200 (2006) 3084–3094<br />

Keywords: Aluminum; Sol-gel processes; Water <strong>chemistry</strong>;<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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