Balancing act: influence of Cu content in NiCu/C catalysts for methane decomposition.

Thermal catalytic decomposition of methane is an innovative pathway to produce CO2-free hydrogen from natural gas. We investigated the role of Cu content in carbon-supported bimetallic NiCu catalysts. A graphitic carbon material was used as a model support, and we combined operando methane decomposition experiments in a thermogravimetric analyzer with in situ electron microscopy measurements. The carbon yield was maximum with around 30% Cu in the nanoparticles. Adding more Cu drastically lowered the carbon solubility in the metal nanoparticles, which lowered the initial reaction rate and overall carbon yield. In situ TEM measurements showed that the addition of Cu to the catalysts strongly influenced the metal nanoparticle shape and size during carbon growth, and the growth mode. NiCu particles were larger, remained spherical and facilitated steady CNF growth. In contrast, pure Ni nanoparticles fluctuated in shape, sometimes fragmented, and showed stuttering CNF growth. This was ascribed to fluctuating coverage of part of the Ni nanoparticle surface with amorphous carbon, which increased the chance of total encapsulation and hence deactivation of the individual Ni nanoparticles. This supports a picture where balancing the carbon supply, transport, and nucleation of amorphous and crystalline carbon is crucial. Our results also highlight the importance of combining statistically relevant measurements with microscopic information on individual nanoparticles to understand overall catalytic trends from the combined behavior of individual catalyst nanoparticles.

An In Situ TEM Study of the Influence of Water Vapor on Reduction of Nickel Phyllosilicate - Retarded Growth of Metal Nanoparticles at Higher Rates.

Unavoidable water formation during the reduction of solid catalyst precursors has long been known to influence the nanoparticle size and dispersion in the active catalyst. This in situ transmission electron microscopy study provides insight into the influence of water vapor at the nanoscale on the nucleation and growth of the nanoparticles (2-16 nm) during the reduction of a nickel phyllosilicate catalyst precursor under H2/Ar gas at 700 °C. Water suppresses and delays nucleation, but counterintuitively increases the rate of particle growth. After full reduction is achieved, water vapor significantly enhances Ostwald ripening which in turn increases the likelihood of particle coalescence. This study proposes that water leads to formation of mobile nickel hydroxide species, leading to faster rates of particle growth during and after reduction.

Control over the fibrillization yield by varying the oligomeric nucleation propensities of self-assembling peptides.

Self-assembling peptides are an exemplary class of supramolecular biomaterials of broad biomedical utility. Mechanistic studies on the peptide self-assembly demonstrated the importance of the oligomeric intermediates towards the properties of the supramolecular biomaterials being formed. In this study, we demonstrate how the overall yield of the supramolecular assemblies are moderated through subtle molecular changes in the peptide monomers. This strategy is exemplified with a set of surfactant-like peptides (SLPs) with different ß-sheet propensities and charged residues flanking the aggregation domains. By integrating different techniques, we show that these molecular changes can alter both the nucleation propensity of the oligomeric intermediates and the thermodynamic stability of the fibril structures. We demonstrate that the amount of assembled nanofibers are critically defined by the oligomeric nucleation propensities. Our findings offer guidance on designing self-assembling peptides for different biomedical applications, as well as insights into the role of protein gatekeeper sequences in preventing amyloidosis.

Thermal enhancement and quenching of upconversion emission in nanocrystals.

Photoluminescence is a powerful tool in temperature sensing. Recently, the application of upconversion (UC) nanocrystals (NCs) has shown great potential for nanothermometry due to high spatial resolution, superior accuracy, and its non-invasive nature. In addition to spectral changes upon heating, anomalous thermal enhancement of UC emission has been reported for UC NCs, but the underlying mechanism remains unclear. Here, we report on NaY(WO4)2 doped with the Er3+-Yb3+ UC couple in NCs and the bulk material, and investigate the temperature-dependent luminescence in both air and dry nitrogen. For UC NCs in air, strong thermal enhancement of UC emission is observed with good reversibility and accompanied by a lengthening of the decay time for the Er3+ UC emission and Yb3+ IR emission. In contrast, the measurements carried out on NCs in dry nitrogen demonstrate a transition from thermal enhancement in the first cycle to thermal quenching in the subsequent cycles. The thermal quenching is similar to that in bulk materials. Thermogravimetric analysis (TGA) and Fourier transform infrared (FT-IR) measurements reveal the presence of water coupled on the NC surface that evaporates upon heating up to ∼470 K but is readsorbed upon cooling. Based on these observations, we explain the anomalous thermal enhancement of UC NCs in air by quenching of the Yb3+ and Er3+ emissions via surface adsorbed water molecules. The present study highlights the importance of careful characterization of surface adsorbed molecules which is crucial for understanding the luminescence properties of NCs, and enables the exploration of UC NCs with higher quantum efficiencies.