Charles A. Mims

Rapid oxygen ion diffusion and surface exchange kinetics in PrBaCo2O5+x with a perovskite related structure and ordered A cations

As part of an investigation of new cathode materials for intermediate temperature solid oxide fuel cells, we have investigated particular perovskite oxides with ordered A cations which, in turn, localize the oxygen vacancies into layers. The oxygen exchange kinetics of polycrystalline samples of the oxygen-deficient double perovskite PrBaCo2O5+x (PBCO) have been determined by electrical conductivity relaxation (ECR) and by oxygen-isotope exchange and depth profiling (IEDP). The ECR and IEDP measurements reveal that PBCO has high electronic conductivity and rapid oxygen ion diffusion and surface exchange kinetics. Both techniques demonstrate that the oxygen kinetics in this structure type are significantly faster than in corresponding disordered perovskites.

The Role of Catalysts and Peroxide Oxidation in Lithium–Oxygen Batteries

A promotor for lithium batteries: nanocrystalline cobalt(II,III) oxide supported on graphene enhances the transport kinetics for both oxygen reduction and oxygen evolution in the lithium-oxygen cell. On cycling the lithium-oxygen cell, the effect of the promoter is, however, eventually overwhelmed by side reactions in the cell, such as, the deposition of carbonates.

Oxygen exchange kinetics of epitaxial PrBaCo2O5+δ thin films

The oxygen exchange kinetics of thin films of the oxygen-deficient double perovskite PrBaCo2O5+δ (PBCO) have been determined by electrical conductivity relaxation (ECR) and by oxygen-isotope exchange and depth profiling (IEDP). Microstructural studies indicate that the PBCO films, prepared by pulsed laser deposition, have excellent single-crystal quality and epitaxial nature. The ECR and IEDP measurements reveal that the PBCO films have high electronic conductivity and rapid surface exchange kinetics, although the ECR data indicate the presence of two distinct kinetic pathways. The rapid surface kinetics compared with those of other perovskites suggest the application of PBCO as a cathode material in intermediate-temperature solid oxide fuel cells.

The Rational Design of a Single-Component Photocatalyst for Gas-Phase CO2 Reduction Using Both UV and Visible Light

The solar‐to‐chemical energy conversion of greenhouse gas CO2 into carbon‐based fuels is a very important research challenge, with implications for both climate change and energy security. Herein, the key attributes of hydroxides and oxygen vacancies are experimentally identified in non‐stoichiometric indium oxide nanoparticles, In2O3‐x(OH)y, that function in concert to reduce CO2 to CO under simulated solar irradiation.

Photomethanation of Gaseous CO2 over Ru/Silicon Nanowire Catalysts with Visible and Near‐Infrared Photons

Gaseous CO2 is transformed photochemically and thermochemically in the presence of H2 to CH4 at millimole per hour per gram of catalyst conversion rates, using visible and near‐infrared photons. The catalyst used to drive this reaction comprises black silicon nanowire supported ruthenium. These results represent a step towards engineering broadband solar fuels tandem photothermal reactors that enable a three‐step process involving i) CO2 capture, ii) gaseous water splitting into H2, and iii) reduction of gaseous CO2 by H2.

Application of Time-of-Flight-Secondary Ion Mass Spectrometry for the Detection of Enzyme Activity on Solid Wood Substrates

Time-of-flight-secondary ion mass spectrometry (TOF-SIMS) is a surface analysis technique that is herein demonstrated to be a viable tool for the detection of enzyme activity on solid substrates. Proof-of-principle experiments are presented that utilize commercial cellulase and laccase enzymes, which are known to modify major polymeric components of wood (i.e., cellulose and lignin, respectively). Enzyme activity is assessed through principle component analysis (PCA) as well as through peak ratios intended to measure selective enzymatic wood degradation. Spectral reproducibility of the complex wood substrates is found to be within 5% relative standard deviation (RSD), allowing for relative quantification of changes in wood composition. Procedures are also presented to identify and avoid the influence of mass interferences from protein adsorption by the enzyme solutions. The activity of a cellulase cocktail is clearly evident through the TOF-SIMS spectra and is supported by high-pressure liquid chromatography (HPLC) measurements of sugar release and by complementary X-ray photoelectron spectroscopy (XPS) measurements of the wood surfaces. Laccase activity, which is mediated through small organic molecules, can be detected in the TOF-SIMS spectra through a decrease in G and S lignin peaks. This work has positive implications for the development of qualitative, high-throughput screening assays for enzyme activity on industrially relevant, lignocellulosic substrates.

Residence times and coverage by surface intermediates during the Fischer-Tropsch synthesis

Isotope tracing of alkene readsorption has been used to examine reversibility in the growth of higher hydrocarbons in the Fischer-Tropsch synthesis. Some reversibility is indicated, but the degree is insufficient to change previous conclusions from isotope transient studies; namely that the surface concentrations of the growing hydrocarbon oligomers during the reaction are very small.

Spatial Separation of Charge Carriers in In2O3–x(OH)y Nanocrystal Superstructures for Enhanced Gas-Phase Photocatalytic Activity

The development of strategies for increasing the lifetime of photoexcited charge carriers in nanostructured metal oxide semiconductors is important for enhancing their photocatalytic activity. Intensive efforts have been made in tailoring the properties of the nanostructured photocatalysts through different ways, mainly including band-structure engineering, doping, catalyst-support interaction, and loading cocatalysts. In liquid-phase photocatalytic dye degradation and water splitting, it was recently found that nanocrystal superstructure based semiconductors exhibited improved spatial separation of photoexcited charge carriers and enhanced photocatalytic performance. Nevertheless, it remains unknown whether this strategy is applicable in gas-phase photocatalysis. Using porous indium oxide nanorods in catalyzing the reverse water-gas shift reaction as a model system, we demonstrate here that assembling semiconductor nanocrystals into superstructures can also promote gas-phase photocatalytic processes. Transient absorption studies prove that the improved activity is a result of prolonged photoexcited charge carrier lifetimes due to the charge transfer within the nanocrystal network comprising the nanorods. Our study reveals that the spatial charge separation within the nanocrystal networks could also benefit gas-phase photocatalysis and sheds light on the design principles of efficient nanocrystal superstructure based photocatalysts.

Heterogeneous reduction of carbon dioxide by hydride-terminated silicon nanocrystals

Silicon constitutes 28% of the earths mass. Its high abundance, lack of toxicity and low cost coupled with its electrical and optical properties, make silicon unique among the semiconductors for converting sunlight into electricity. In the quest for semiconductors that can make chemicals and fuels from sunlight and carbon dioxide, unfortunately the best performers are invariably made from rare and expensive elements. Here we report the observation that hydride-terminated silicon nanocrystals with average diameter 3.5 nm, denoted ncSi:H, can function as a single component heterogeneous reducing agent for converting gaseous carbon dioxide selectively to carbon monoxide, at a rate of hundreds of μmol h−1 g−1. The large surface area, broadband visible to near infrared light harvesting and reducing power of SiH surface sites of ncSi:H, together play key roles in this conversion. Making use of the reducing power of nanostructured hydrides towards gaseous carbon dioxide is a conceptually distinct and commercially interesting strategy for making fuels directly from sunlight.

Oxygen pathways in methane selective oxidation over silica-supported molybdena

Oxygen pathways for CH4 partial oxidation over a silica-supported molybdena catalyst were investigated using a series of oxygen isotopic exchange experiments and steady state oxygen isotope transients. The initial source of oxygen in the products is masked by rapid and extensive oxygen exchange between the catalyst and the products CO2 and HCHO. This exchange process occurs at the surface molybdena site and is accompanied by rapid O interchange between the surface and support phases which allows access to the bulk of the support. Laser desorption Fourier transform mass spectra, LDFTMS, indicate equal enrichment of18O in both the silica and molybdena fragments.