Stabilizing Single Ni Adatoms on a Two-Dimensional Porous Titania Overlayer at the SrTiO3(110) Surface

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Wang, Zhiming
Hao, Xianfeng
Gerhold, Stefan
Mareš, Petr
Wagner, Margareta
Bliem, Roland
Schulte, Karina
Schmid, Michael
Franchini, Cesare
Diebold, Ulrike

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Nickel vapor-deposited on the SrTiO3(110) surface was studied using scanning tunneling microscopy, photoemission spectroscopy (PES), and density functional theory calculations. This surface forms a (4 x 1) reconstruction, composed of a 2-D titania structure with periodic six- and ten-membered nanopores. Anchored at these nanopores, Ni single adatoms are stabilized at room temperature. PES measurements show that the Ni adatoms create an in-gap state located at 1.9 eV below the conduction band minimum and induce an upward band bending. Both experimental and theoretical results suggest that Ni adatoms are positively charged. Our study produces well-dispersed singleadatom arrays on a well-characterized oxide support, providing a model system to investigate single-adatom catalytic and magnetic properties.
Nickel vapor-deposited on the SrTiO3(110) surface was studied using scanning tunneling microscopy, photoemission spectroscopy (PES), and density functional theory calculations. This surface forms a (4 x 1) reconstruction, composed of a 2-D titania structure with periodic six- and ten-membered nanopores. Anchored at these nanopores, Ni single adatoms are stabilized at room temperature. PES measurements show that the Ni adatoms create an in-gap state located at 1.9 eV below the conduction band minimum and induce an upward band bending. Both experimental and theoretical results suggest that Ni adatoms are positively charged. Our study produces well-dispersed singleadatom arrays on a well-characterized oxide support, providing a model system to investigate single-adatom catalytic and magnetic properties.

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Journal of Physical Chemistry C. 2014, vol. 118, issue 34, p. 19904-19909.
https://pubs.acs.org/doi/10.1021/jp506234r

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en

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Except where otherwised noted, this item's license is described as Creative Commons Attribution 4.0 International
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