Portable gas chromatograph calibration with gases of varying viscosities.

The quantitative analysis of gas mixtures with gas chromatography is based on the calibration with certified standards and the determination of a response relationship for each species by regression analysis. The conventional assumption of a constant amount-of-substance injected onto the column, the sample size, for all standards analyzed represents one of the largest sources of uncertainies in this analysis technique. For systems using time-based microinjectors, the sample size injected onto the column is determined by the opening time of a pneumatically actuated microvalve and therefore depends upon the gas velocity developed in the injector's microchannel.

Kinetics and Mechanism of Metal Nanoparticle Growth Optical Extinction Spectroscopy and Computational Modeling: The Curious Case of Colloidal Gold.

An overarching computational framework unifying several optical theories to describe the temporal evolution of gold nanoparticles (GNPs) during a seeded growth process is presented. To achieve this, we used the inexpensive and widely available optical extinction spectroscopy, to obtain quantitative kinetic data. spectra collected over a wide set of experimental conditions were regressed using the physical model, calculating light extinction by ensembles of GNPs during the growth process.

Enhanced Proton Conductivity in Y-Doped BaZrO via Strain Engineering.

The effects of stress-induced lattice distortions (strain) on the conductivity of Y-doped BaZrO, a high-temperature proton conductor with key technological applications for sustainable electrochemical energy conversion, are studied. Highly ordered epitaxial thin films are grown in different strain states while monitoring the stress generation and evolution in situ. Enhanced proton conductivity due to lower activation energies is discovered under controlled conditions of tensile strain.

Double modulation pyrometry: A radiometric method to measure surface temperatures of directly irradiated samples.

The design, implementation, calibration, and assessment of double modulation pyrometry to measure surface temperatures of radiatively heated samples in our 1 kW imaging furnace is presented. The method requires that the intensity of the external radiation can be modulated. This was achieved by a rotating blade mounted parallel to the optical axis of the imaging furnace.

Increasing the Sensitivity to Short-Lived Species in a Modulated Excitation Experiment.

The combination of spectroscopic and diffraction methods to study chemical transformations is fundamental for the understanding of reaction mechanisms. The identification of short-lived species, likely active species, is often hindered by the contribution of spectator species not directly involved in the reaction. The present study considers two different approaches to obtain increased sensitivity to transient species for experiments obeying the modulated excitation paradigm and exploiting phase sensitive detection (PSD).

Determination of Conduction and Valence Band Electronic Structure of LaTiO N Thin Film.

The nitrogen substitution into the oxygen sites of several oxide materials leads to a reduction of the band gap to the visible-light energy range, which makes these oxynitride semiconductors potential photocatalysts for efficient solar water splitting. Oxynitrides typically show a different crystal structure compared to the pristine oxide material. As the band gap is correlated to both the chemical composition and the crystal structure, it is not trivial to distinguish which modifications of the electronic structure induced by the nitrogen substitution are related to compositional and/or structural effects.

Investigating the behavior of various cocatalysts on LaTaON photoanode for visible light water splitting.

We performed a comparative study on the photoelectrochemical performance of LaTaON loaded with NiO, NiFeO, CoO and IrO as cocatalysts. Ni-based oxides lead to the highest improvement on the photoelectrochemical performance, while CoO and IrO also enhance the performance though to a lower extent, but they simultaneously introduce more pseudocapacitive current thus resulting in an inefficient utilization of the photo-generated holes. Repetitive voltage cycling between 1.

Synchrotron-Based Highest Resolution Terahertz Spectroscopy of the ν Band System of 1,2-Dithiine (CHS): A Candidate for Measuring the Parity Violating Energy Difference between Enantiomers of Chiral Molecules.

The chiral C symmetric molecule 1,2-dithiine (1,2-dithia-3,5-hexadiene, CHS) has been identified as a possible candidate for measuring the parity violating energy difference between enantiomers. We report here the observation and analysis of the low-frequency fundamental ν using highest resolution synchrotron-based interferometric Fourier transform infrared (FTIR) spectroscopy in the terahertz range with a band center of ν = 6.95375559 THz (ν̃ = 231.

Highly sensitive SnO2 sensor via reactive laser-induced transfer.

Gas sensors based on tin oxide (SnO2) and palladium doped SnO2 (Pd:SnO2) active materials are fabricated by a laser printing method, i.e. reactive laser-induced forward transfer (rLIFT).

In situ stress observation in oxide films and how tensile stress influences oxygen ion conduction.

Many properties of materials can be changed by varying the interatomic distances in the crystal lattice by applying stress. Ideal model systems for investigations are heteroepitaxial thin films where lattice distortions can be induced by the crystallographic mismatch with the substrate. Here we describe an in situ simultaneous diagnostic of growth mode and stress during pulsed laser deposition of oxide thin films.

Crystallization of zirconia based thin films.

The crystallization kinetics of amorphous 3 and 8 mol% yttria stabilized zirconia (3YSZ and 8YSZ) thin films grown by pulsed laser deposition (PLD), spray pyrolysis and dc-magnetron sputtering are explored. The deposited films were heat treated up to 1000 °C ex situ and in situ in an X-ray diffractometer. A minimum temperature of 275 °C was determined at which as-deposited amorphous PLD grown 3YSZ films fully crystallize within five hours.

Reinvestigation of the elementary chemical kinetics of the reaction C2H5(•) + HBr (HI) → C2H6 + Br(•) (I(•)) in the range 293-623 K and its implication on the thermochemical parameters of C2H5(•) free radical.

A reinvestigation of the absolute rate constants of the metathesis reactions C2H5• + HBr → C2H6 + Br• (R1) and C2H5• + HI → C2H6 + I• (R2) has been performed and led to the following Arrhenius expressions: k1 = 3.69(±0.95) × 10–11 exp(−10.

Strain-induced ferromagnetism in antiferromagnetic LuMnO3 thin films.

Single phase and strained LuMnO(3) thin films are discovered to display coexisting ferromagnetic and antiferromagnetic orders. A large moment ferromagnetism (≈1μ(B)), which is absent in bulk samples, is shown to display a magnetic moment distribution that is peaked at the highly strained substrate-film interface. We further show that the strain-induced ferromagnetism and the antiferromagnetic order are coupled via an exchange field, therefore demonstrating strained rare-earth manganite thin films as promising candidate systems for new multifunctional devices.

Sequential printing by laser-induced forward transfer to fabricate a polymer light-emitting diode pixel.

Patterned deposition of polymer light-emitting diode (PLED) pixels is a challenge for electronic display applications. PLEDs have additional problems requiring solvent orthogonality of different materials in adjacent layers. We present the fabrication of a PLED pixel by the sequential deposition of two different layers with laser-induced forward transfer (LIFT), a "dry" deposition technique.

Partially reduced graphite oxide as an electrode material for electrochemical double-layer capacitors.

Partially reduced graphite oxide was prepared from graphite oxide by using synthetic graphite as precursor. The reduction of graphite oxide with a layer distance of 0.57 nm resulted in a reduction of the layer distance depending on the degree of reduction.

Electronic structure and oxygen vacancies in PdO and ZnO: validation of DFT models.

PdO is one of the most important catalytic materials currently used in the industry. In redox catalytic reactions involving PdO, the bulk phase is an additional source of oxygen. This leads to strong transformations not only at the surface of PdO but also in the near sub-surface and bulk regions.

Reaction of SO4˙⁻ with an oligomer of poly(sodium styrene sulfonate). Probing the mechanism of damage to fuel cell membranes.

Clarification of the mechanism of degradation of model compounds for polymers used in polymer electrolyte fuel cells may identify intermediates that propagate damage; such knowledge can be used to improve the lifetime of fuel cell membranes, a central issue to continued progress in fuel cell technology. In proton-exchange membranes based on poly(styrene sulfonic acid), hydroxycyclohexadienyl radicals are formed after reaction with HO˙ and thought to decay to short-lived radical cations at low pH. To clarify subsequent reactions, we generated radical cations by reaction of SO(4)˙(-) with oligomers of poly(styrene sulfonic acid) (MW ≈ 1100 Da).

Using 2H labeling with neutron radiography for the study of solid polymer electrolyte water transport properties.

A method combining (2)H labeling of different sources of H atoms (hydrogen, water vapor) with neutron imaging for the analysis of transport parameters in the bulk and at the interfaces of Nafion polymer electrolyte membranes is proposed. The use of different isotope compositions in the steady state allows evaluation of the relation between bulk and interface transport parameters, but relies on literature data for evaluating absolute values. By using transients of isotope composition, absolute values of these parameters including the self-diffusion coefficient of H can be extracted, making this method an attractive alternative to self-diffusion measurements using nuclear magnetic resonance (NMR), allowing measurements in precisely controlled conditions in real fuel cell structures.

Evaporation of urea at atmospheric pressure.

Aqueous urea solution is widely used as reducing agent in the selective catalytic reduction of NO(x) (SCR). Because reports of urea vapor at atmospheric pressure are rare, gaseous urea is usually neglected in computational models used for designing SCR systems. In this study, urea evaporation was investigated under flow reactor conditions, and a Fourier transform infrared (FTIR) spectrum of gaseous urea was recorded at atmospheric pressure for the first time.

Laser-induced forward transfer of polymer light-emitting diode pixels with increased charge injection.

Laser-induced forward transfer (LIFT) has been used to print 0.6 mm × 0.5 mm polymer light-emitting diode (PLED) pixels with poly[2-methoxy, 5-(2-ethylhexyloxy)-1,4-phenylene vinylene] (MEH-PPV) as the light-emitting polymer.

Damage to fuel cell membranes. Reaction of HO* with an oligomer of poly(sodium styrene sulfonate) and subsequent reaction with O(2).

An understanding of the reactivity of oligomeric compounds that model fuel cell membrane materials under oxidative-stress conditions that mimic the fuel cell operating environment can identify material weaknesses and yield valuable insights into how a polymer might be modified to improve oxidative stability. The reaction of HO˙ radicals with a polymer electrolyte fuel cell membrane represents an initiation step for irreversible membrane oxidation. By means of pulse radiolysis, we measured k = (9.

Chemical and structural changes of quartz surfaces due to structuring by laser-induced backside wet etching.

Various physical and chemical processes which are involved in laser-induced backside wet etching are investigated. The surface of quartz etched by the laser-induced backside wet etching using a XeCl excimer laser at various fluences is analyzed by Raman microscopy, X-ray photoelectron spectroscopy and fiber-tip attenuated total-reflection Fourier-transform infrared spectroscopy. The investigations reveal the formation of a high amount of amorphous carbon deposits at low laser fluences, which strongly adhere to the quartz surface.

Determination of the bulk cobalt valence state of co-perovskites containing surface-adsorbed impurities.

We used thermogravimetric hydrogen reduction and iodometric titration to determine the bulk valence state of cobalt in Co-perovskites containing surface carbonate hydroxide or hydroxyl groups. It could be shown that thermogravimetric hydrogen reduction experiments are very sensitive to volatile surface groups, but due to their volatility, they can be specified and the bulk valence state of cobalt can still be deduced from these experiments. The iodometric titration is less sensitive to small volatile surface impurities, but precaution has to be taken that oxygen or iodine does not escape from the solution during dissolution of the sample.

Measured total cross sections of slow neutrons scattered by solid deuterium and implications for ultracold neutron sources.

The total scattering cross sections for slow neutrons with energies in the range 100 neV to 3 meV for solid ortho-2H2 at 18 and 5 K, frozen from the liquid, have been measured. The 18 K cross sections are found to be in excellent agreement with theoretical expectations and for ultracold neutrons dominated by thermal up scattering. At 5 K the total scattering cross sections are found to be dominated by the crystal defects originating in temperature induced stress but not deteriorated by temperature cycles between 5 and 10 K.