What could be the low-temperature limit of atomic layer deposition of platinum using MeCpPtMe and oxygen?

We explore the low-temperature limit of atomic layer deposition of Pt using MeCpPtMe and O. We reveal that by supplying a sufficiently high O exposure, highly dispersed and thermally stable Pt sub-nanometer clusters can be deposited onto the surface of P25 TiO nanoparticles even at room temperature by atmospheric-pressure ALD.

Variable temperature TEM mapping of the thermodynamically stable element distribution in bimetallic Pt-Rh nanoparticles.

We report here the first variable temperature transmission electron microscopy (TEM) study on smaller Pt-Rh nanoparticles (≤24 nm) under vacuum conditions. Well-defined 50 at% Pt/50 at% Rh Pt-Rh solid solution and Rh(core)-Pt(shell) nanoparticles, obtained colloidal synthesis routes, were investigated between room temperature and 650 °C to elucidate the tendency of elemental mixing/segregation. Key findings are that Pt-Rh nanoparticles <13 nm are stable in a solid solution configuration over the entire studied temperature range, whereas nanoparticles >13 nm tend to segregate upon cooling.

One-pot synthesis of cobalt-rhenium nanoparticles taking the unusual β-Mn type structure.

Using a facile one-pot colloidal method, it is now possible to obtain monodisperse Co Re nanoparticles (NPs), with excellent control of Re stoichiometry for < 0.15. Re-incorporation in terms of a solid solution stabilizes the β-Mn polymorph relative to the hcp/ccp variants of cobalt.

In situ TEM observation of the Boudouard reaction: multi-layered graphene formation from CO on cobalt nanoparticles at atmospheric pressure.

Using a MEMS nanoreactor in combination with a specially designed in situ Transmission Electron Microscope (TEM) holder and gas supply system, we imaged the formation of multiple layers of graphene encapsulating a cobalt nanoparticle, at 1 bar CO : N (1 : 1) and 500 °C. The cobalt nanoparticle was imaged live in a TEM during the Boudouard reaction. The in situ/operando TEM studies give insight into the behaviour of the catalyst at the nanometer-scale, under industrially relevant conditions.

Intermediate stages of electrochemical oxidation of single-crystalline platinum revealed by in situ Raman spectroscopy.

Understanding the atomistic details of how platinum surfaces are oxidized under electrochemical conditions is of importance for many electrochemical devices such as fuel cells and electrolysers. Here we use in situ shell-isolated nanoparticle-enhanced Raman spectroscopy to identify the intermediate stages of the electrochemical oxidation of Pt(111) and Pt(100) single crystals in perchloric acid. Density functional theory calculations were carried out to assist in assigning the experimental Raman bands by simulating the vibrational frequencies of possible intermediates and products.

Iridium-based double perovskites for efficient water oxidation in acid media.

The development of active, cost-effective and stable oxygen-evolving catalysts is one of the major challenges for solar-to-fuel conversion towards sustainable energy generation. Iridium oxide exhibits the best available compromise between catalytic activity and stability in acid media, but it is prohibitively expensive for large-scale applications. Therefore, preparing oxygen-evolving catalysts with lower amounts of the scarce but active and stable iridium is an attractive avenue to overcome this economical constraint.

Supercrystals of CdSe quantum dots with high charge mobility and efficient electron transfer to TiO2.

Thermal annealing of thin films of CdSe/CdS core/shell quantum dots induces superordering of the nanocrystals and a significant reduction of the interparticle spacing. This results in a drastic enhancement of the quantum yield for charge carrier photogeneration and the charge carrier mobility. The mobile electrons have a mobility as high as 0.

Nanoscale chemical imaging of a working catalyst by scanning transmission X-ray microscopy.

The modern chemical industry uses heterogeneous catalysts in almost every production process. They commonly consist of nanometre-size active components (typically metals or metal oxides) dispersed on a high-surface-area solid support, with performance depending on the catalysts' nanometre-size features and on interactions involving the active components, the support and the reactant and product molecules. To gain insight into the mechanisms of heterogeneous catalysts, which could guide the design of improved or novel catalysts, it is thus necessary to have a detailed characterization of the physicochemical composition of heterogeneous catalysts in their working state at the nanometre scale.

Salinity-dependent diatom biosilicification implies an important role of external ionic strength.

The role of external ionic strength in diatom biosilica formation was assessed by monitoring the nanostructural changes in the biosilica of the two marine diatom species Thalassiosira punctigera and Thalassiosira weissflogii that was obtained from cultures grown at two distinct salinities. Using physicochemical methods, we found that at lower salinity the specific surface area, the fractal dimensions, and the size of mesopores present in the biosilica decreased. Diatom biosilica appears to be denser at the lower salinity that was applied.