Phase masks for electron microscopy fabricated by thermal scanning probe lithography.

Nano-structured phase masks offer intriguing possibilities in electron-beam shaping. The fabrication of such phase masks is typically achieved by focused (Ga+-)ion beam milling of thin membranes. To overcome the problem of Ga implantation in the phase mask, we explore the fabrication of silicon-nitride phase masks using thermal scanning probe lithography combined with wet and dry etching. The functionality of the phase masks is demonstrated by generation of electron Vortex and Bessel beams. Major benefit of thermal scanning probe lithography in addition to the absence of ion implantation is the high accuracy and control over the patterned structure and depth.

Reaction-induced cluster ripening and initial size-dependent reaction rates for CO oxidation on Pt(n)/TiO2(110)-(1×1).

We determined the CO oxidation rates for size-selected Ptn (n ∈ {3,7,10}) clusters deposited onto TiO2(110). In addition, we investigated the cluster morphologies and their mean sizes before and after the reaction. While the clusters are fairly stable upon annealing in ultrahigh vacuum up to 600 K, increasing the temperature while adsorbing either one of the two reactants leads to ripening already from 430 K on. This coarsening is even more pronounced when both reactants are dosed simultaneously, i.e., running the CO oxidation reaction. Since the ripening depends on the size initially deposited, there is nevertheless a size effect; the catalytic activity decreases monotonically with increasing initial cluster size.

Effect of the TiO2 reduction state on the catalytic CO oxidation on deposited size-selected Pt clusters.

The catalytic activity of deposited Pt(7) clusters has been studied as a function of the reduction state of the TiO(2)(110)-(1 × 1) support for the CO oxidation reaction. While a slightly reduced support gives rise to a high catalytic activity of the adparticles, a strongly reduced one quenches the CO oxidation. This quenching is due to thermally activated diffusion of Ti(3+) interstitials from the bulk to the surface where they deplete the oxygen adsorbed onto the clusters by the formation of TiO(x) (x ≃ 2) structures. This reaction is more rapid than the CO oxidation. The present results are of general relevance to heterogeneous catalysis on TiO(2)-supported metal clusters and for reactions involving oxygen as intermediate.