Insets are the H = K = 1 (radius = √2 reciprocal lattice units) circle scans for

L = 3 showing that Pt in-plane ordering is equivalent to STO as all peaks are separated by 90°. STO (200) is aligned to the direction of ϕ = 0. Conclusions We have demonstrated a simple method for the preparation of platinum nanoparticle arrays with control of nanoparticle size, spacing, and shape. This method can be used to produce monodisperse platinum catalyst nanoparticles without need for elaborate nanopatterning equipment. Particle size and spacing can be controlled by the size of the silica beads used to form the monolayer template. The silica monolayers deposited at optimized conditions on Nb-doped STO were used as masks for deposition of epitaxial platinum islands. Because of initial epitaxial relation between platinum and STO, and annealing conditions, www.selleckchem.com/products/bi-d1870.html cubooctahedral platinum nanoparticles form. The platinum nanocrystal arrays were characterized by scanning electron microscopy and synchrotron X-ray scattering indicating that they are single crystalline and oriented. Because the STO substrate is electrochemically inactive in a very wide range of

potentials in PF-02341066 manufacturer aqueous electrolytes, platinum nanoparticle arrays can be used as well-defined model electrocatalysts to study technologically important reactions such as oxygen reduction reaction, oxygen and hydrogen evolution reaction, or carbon monoxide oxidation. These reactions are important in operations of fuel cells and electrolyzers where platinum metal is the main constituent of deployed catalysts. Acknowledgements The authors would like to thank to Dr. Sungsik Lee for the help during X-ray experiments Resveratrol at APS. The work at Safarik University was supported by Slovak Grant VEGA No. 1/0782/12, by the grant of the Slovak Research and Development Agency under Contract No. APVV-0132-11, by project CFNT MVEP – the Centre of Excellence of the Slovak Academy of Sciences, and by the

ERDF EU Grant under Contract No. ITMS26220120005. The work in Materials Science Division and the use of the Advanced Photon Source and Electron Microscopy Center at Argonne National Laboratory were supported by the US Department of Energy, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. References 1. Strmcnik DS, Tripkovic DV, Van Der Vliet D, Chang KC, Komanicky V, You H, Karapetrov G, Greeley JP, Stamenkovic VR, Marković NM: Unique activity of platinum adislands in the CO electrooxidation reaction. J Am Chem Soc 2008,130(46):15332–15339.CrossRef 2. Komanicky V, Iddir H, Chang KC, Menzel A, Karapetrov G, Hennessy D, Zapol P, You H: Shape-dependent activity of platinum array catalyst. J Am Chem Soc 2009,131(16):5732–5733.CrossRef 3. Iddir H, Komanicky V, Oǧüt S, You H, Zapol PS: Shape of platinum nanoparticles supported on SrTiO 3 : experimental and theory. J Phys Chem C 2007,111(40):14782–14789.CrossRef 4.