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4th EucheMs chemistry congress

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thursday, 30-Aug 2012<br />

s850<br />

chem. Listy 106, s587–s1425 (2012)<br />

solid state Chemistry Materials <strong>chemistry</strong>/New materials<br />

solid state Chemistry and Nano<strong>chemistry</strong><br />

o - 5 1 9<br />

MetAL-ASSiSted Growth of GerMAniuM<br />

nAnowireS: oPPortunitieS uSinG SoLid MetAL<br />

SeedS<br />

S. BArth 1<br />

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

Chemistry, Vienna, Austria<br />

One-dimensional (1D) semiconductor nano-architectures<br />

with tunable morphologies, dimensions, crystallographic phases<br />

and orientation are of tremendous interest for a broad range of<br />

applications. [1] Metal-seeded growth of 1D semiconductor<br />

nanostructures is still a very active field of research, despite the<br />

huge progress which has been made in understanding this<br />

fundamental phenomenon. Liquid growth promoters allow control<br />

of the aspect ratio, diameter and structure of 1D crystals via<br />

external parameters, such as precursor feedstock, temperature and<br />

operating pressure. However the transfer of crystallographic<br />

information from a nanoparticle seed to a growing nanowire has<br />

not been described in the literature. We investigated the formation<br />

of Ge nanowires using solid metal growth promoters in a process<br />

based on thermal decomposition of diphenylgermane. The<br />

theoretical requirements for transferring information such as<br />

defects from nanoparticle seeds to growing semiconductor<br />

nanowires have been defined and we describe why specific metal<br />

nanoparticles are ideal candidates for this purpose. [2] Significantly,<br />

under certain reaction conditions {111} stacking faults in the<br />

noble metal seeds can be directly transferred to a high percentage<br />

of -oriented Ge nanowires, in the form of radial twins in<br />

the semiconductor crystals. In addition, we will detail the<br />

influence of solid growth seeds on the crystal quality of Ge<br />

nanowires and demonstrate size-selective growth in the sub-20 nm<br />

diameter regime. [3] Controlled defect transfer from nanoparticles<br />

to nanowires could open up the possibility of engineering 1D<br />

nanostructures with new and tuneable physical properties and<br />

morphologies.<br />

references:<br />

1. S. Barth, F. Hernandez-Ramirez, J. D. Holmes,<br />

A. Romano-Rodriguez. Prog. Mater. Sci. 2010, 55,<br />

563–627.<br />

2. S. Barth, J. J. Boland, J. D. Holmes. Nano Lett. 2011, 11,<br />

1550-1555.<br />

3. S. Barth, M. M. Kolesnik, K. Donegan, V. Krstic,<br />

J. D. Holmes. Chem. Mater. 2011, 23, 3335–3340.<br />

Keywords: Crystal growth; Chemical vapor deposition;<br />

Nanostructures; Electron diffraction;<br />

solid state Chemistry and Nano<strong>chemistry</strong><br />

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

o - 5 2 0<br />

StruCturAL ChArACterizAtion And<br />

trAnSPort ProPertieS of Cvt Grown zrSe3<br />

And zrS3 CryStALS.<br />

A. dASAdiA 1 , B. nAriyA 1 , A. JAni 1<br />

1 Sardar Patel University, Department Of Physics, Vallabh<br />

Vidyanagar, India<br />

Single crystals of ZrSe3 and ZrS3 are family of materials<br />

with low symmetry structure were grown by chemical vapour<br />

transport technique using iodine as a transporting agent. The<br />

grown crystals were characterized by energy dispersive analysis<br />

of X-ray (EDAX) for confirmation of stochiometric proportion of<br />

constituent elements and structure of grown crystals was<br />

determined by X-ray diffraction (XRD) technique. The resistivity<br />

and thermoelectric power measurements were carried out in the<br />

temperature range 308 K to 573 K. The Hall coefficient, carrier<br />

concentration and Hall mobility were determined from Hall Effect<br />

measurements at room temperature.<br />

Keywords: Crystal Growth; CVT; structure characterization;<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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