Catalytic activity of nanostructured Au: Scale effects versus bimetallic/bifunctional effects in low-temperature CO oxidation on nanoporous Au

• Lu-Cun Wang,
• Yi Zhong,
• Haijun Jin,
• Daniel Widmann,
• Jörg Weissmüller and
• R. Jürgen Behm

Beilstein J. Nanotechnol. 2013, 4, 111–128, doi:10.3762/bjnano.4.13

• be significantly influenced by the mass transport limitation by pore diffusion [29]. For the diluted powders of NPG samples used in this work, however, diffusion limitations are much less likely than for NPG disks used in a previous study [29]. In fact, by using the method described before [29], the

• Thiele modulus is estimated to be less than 3, where the influence of mass transport limitations is negligible. Figure 5a shows the CO oxidation activity of the four NPG(Ag) catalysts, in terms of Au mass-normalized reaction rates, and their temporal evolution in a standard reaction mixture (1% CO, 1% O2

Characterization and properties of micro- and nanowires of controlled size, composition, and geometry fabricated by electrodeposition and ion-track technology

• Maria Eugenia Toimil-Molares

Beilstein J. Nanotechnol. 2012, 3, 860–883, doi:10.3762/bjnano.3.97

Focused electron beam induced deposition: A perspective

• Michael Huth,
• Fabrizio Porrati,
• Christian Schwalb,
• Marcel Winhold,
• Roland Sachser,
• Maja Dukic,
• Jonathan Adams and
• Georg Fantner

Beilstein J. Nanotechnol. 2012, 3, 597–619, doi:10.3762/bjnano.3.70

• termed as the reaction-rate-limited (RRL) regime. For longer dwell times the precursor adsorbate becomes depleted as a consequence of the dissociation rate exceeding the replenishment rate. The resulting growth regime is mass-transport-limited (MTL). Since the characteristic dwell time for which, at a

Nanostructured, mesoporous Au/TiO₂ model catalysts – structure, stability and catalytic properties

• Matthias Roos,
• Dominique Böcking,
• Kwabena Offeh Gyimah,
• Gabriela Kucerova,
• Joachim Bansmann,
• Johannes Biskupek,
• Ute Kaiser,
• Nicola Hüsing and
• R. Jürgen Behm

Beilstein J. Nanotechnol. 2011, 2, 593–606, doi:10.3762/bjnano.2.63

• positive reaction orders (at 135 °C αCO ≈ 1.0 and αO2 ≈ 0.8). Furthermore, the observation of a linear increase of the activity with increasing film thickness indicates that mass transport limitations inside the film are essentially absent (below the detection limit), and the reaction conditions (partial

Inorganic–organic hybrid materials through post-synthesis modification: Impact of the treatment with azides on the mesopore structure

• Miriam Keppeler,
• Jürgen Holzbock,
• Johanna Akbarzadeh,
• Herwig Peterlik and
• Nicola Hüsing

Beilstein J. Nanotechnol. 2011, 2, 486–498, doi:10.3762/bjnano.2.52

• Inorganic–organic hybrid materials with tailored porosity on several length scales are of interest for a variety of applications, such as separation, adsorption, catalysis, energy storage, etc., due to the benefits arising from each pore size regime, e.g., rapid mass transport through macropores combined

• , progress in the synthesis protocols even allows for the preparation of different macroscopic morphologies such as powders, coatings, fibres, or monoliths. Monoliths are of special interest for functional devices, e.g., as chromatography columns, or catalytic reactors. However, to allow mass transport with

Kinetic lattice Monte-Carlo simulations on the ordering kinetics of free and supported FePt L1₀-nanoparticles

• Michael Müller and
• Karsten Albe

Beilstein J. Nanotechnol. 2011, 2, 40–46, doi:10.3762/bjnano.2.5

• spherical particle is deposited. This can be seen by comparing the time evolution of the long-range order of the spherical with an initially facetted particle. The mass transport from the particle surface towards the substrate is therefore accompanied by a simultaneous adjustment of order. However, after