Production of a monolithic fuel cell stack with high power density.

The transportation sector is undergoing a technology shift from internal combustion engines to electric motors powered by secondary Li-based batteries. However, the limited range and long charging times of Li-ion batteries still hinder widespread adoption. This aspect is particularly true in the case of heavy freight and long-range transportation, where solid oxide fuel cells (SOFCs) offer an attractive alternative as they can provide high-efficiency and flexible fuel choices. However, the SOFC technology is mainly used for stationary applications owing to the high operating temperature, low volumetric power density and specific power, and poor robustness towards thermal cycling and mechanical vibrations of conventional ceramic-based cells. Here, we present a metal-based monolithic fuel cell design to overcome these issues. Cost-effective and scalable manufacturing processes are employed for fabrication, and only a single heat treatment is required, as opposed to multiple thermal treatments in conventional SOFC production. The design is optimised through three-dimensional multiphysics modelling, nanoparticle infiltration, and corrosion-mitigating treatments. The monolithic fuel cell stack shows a power density of 5.6 kW/L, thus, demonstrating the potential of SOFC technology for transport applications.

The Raman spectrum of isolated water clusters.

Cold water oligomers (H2O)n and (D2O)n with n = 2-5 are assigned in spontaneous Raman scattering spectra of seeded rare gas expansions for the first time. Comparison with infrared spectra provides direct experimental insights into the hydrogen bond-mediated excitonic OH oscillator coupling, which is responsible for ultrafast energy transfer between water molecules, usually suppressed by isotopic dilution in femtosecond experiments for the condensed phase. The experimental coupling constants are compared to those in state-of-the-art full-dimensional water potential energy hypersurfaces, leaving room for improvement in the description of the coupled dynamics in water. Evidence for intensified Fermi resonance between OH stretching and OH bending motion beyond water trimers is collected.

Photoionization of small sodium-doped acetic acid clusters.

The uptake of sodium and the fragmentation before and after "soft" photoionization with ultraviolet light are investigated for small acetic acid clusters. The acetic acid clusters are generated in a supersonic expansion and ionized with ultraviolet light after doping with sodium in a pick-up chamber. The composition of the bare acetic acid clusters in the molecular beam is determined independently from complementary photoionization experiments using extreme ultraviolet light. The experimental results are analyzed with the help of density functional calculations for energetics and statistical adiabatic channel calculations for fragmentation kinetics. The study demonstrates that the detected ions originate from fragmentation in the neutral as well as in the ionic state, and in particular that the fragmentation pathway strongly depends on the cluster size.

PFI-ZEKE photoelectron spectrum of CH2F2, ionisation potential and ionic fragmentation appearance potentials.

The first vibrationally resolved pulsed-field-ionisation zero-kinetic-energy (PFI-ZEKE) photoelectron spectrum of difluoromethane from its adiabatic ionisation potential (formation of the C(2v) conformer of CH(2)F(2)(+)) to the onset of the first ionic fragmentation channel is presented. Precise values for the adiabatic ionisation potential (12.7252 +/- 0.0009 eV) and the appearance potentials of the H loss product (13.065 +/- 0.003 eV) and the F loss product (14.30 +/- 0.06 eV) of the cation are reported. Ab initio harmonic calculations were performed at the MP2 level with quadruple-zeta basis sets in an attempt to assign the newly observed vibrational structure which, in its previously published low resolution form, led to numerous speculations regarding its true origin. The adiabatic ionisation potential and the fragmentation appearance potentials for the three lowest dissociation channels are also predicted in the complete basis set limit of CCSD(T) theory.

The stiffness of a fully stretched polyethylene chain: A Raman jet spectroscopy extrapolation.

Linear alkanes with n=5-16 C-atoms are partially relaxed into their stretched all-trans conformation by supersonic jet expansion. Their longitudinal acoustic modes are identified by spontaneous Raman scattering and deperturbed from transverse bending mode components and Fermi resonance with combination states of the same symmetry. Comparison with quantum chemical predictions of the longitudinal modes in hydrocarbon chains with up to 54 C-atoms allows for a reliable extrapolation to the limiting product nnu(n)=2310+/-30 cm(-1) for large n, from which the elastic modulus of an ideal polyethylene chain in vacuum may be estimated at 309+/-8 GPa. Differences to solid state determinations of this quantity are discussed.

Infrared spectra of C2H6, C2H4, C2H2, and CO2 aerosols potentially formed in Titan's atmosphere.

Pure and mixed aerosols of ethane, ethylene, acetylene and carbon dioxide were generated in a collisional cooling cell and characterized by Fourier transform infrared spectroscopy between 600 and 4000 cm(-1). Pure ethane, pure ethylene, and mixed ethane/ethylene initially form supercooled liquid droplets, which over time crystallize to their stable solid phases. These droplets are found to be long-lived (up to hours) for pure ethane and mixed ethane/ethylene, but short-lived (up to seconds) for pure ethylene. Acetylene and carbon dioxide form solid aerosol particles. Acetylene particles have a partially amorphous structure, while carbon dioxide particles are crystalline. The structure of the infrared bands of carbon dioxide is strongly determined by the particles' shape due to exciton coupling. The comparison of various mixed systems reveals that acetylene very efficiently induces heterogeneous crystallization. As reported earlier, the co-condensation of acetylene and carbon dioxide can lead to the formation of a metastable mixed crystalline phase. Our preliminary calculations show that this mixed phase has a monoclinic rather than the cubic structure proposed previously.

Adiabatic ionization potential of acetic acid and torsional dynamics of its cation.

Pulsed-field-ionization zero-kinetic-energy photoelectron spectroscopy and supersonic cooling are used to investigate the CH(3) torsional dynamics of the acetic acid cation and to determine an accurate value for the first adiabatic ionization potential of acetic acid (IP=85 912+/-5 cm(-1)), which has been the subject of debates for more than 40 yr. A doubling of the torsional barrier upon ionization is due to a significant shortening of the C-C bond and reduces the tunneling efficiency by an order of magnitude.

Raman spectroscopic evidence for the most stable water/ethanol dimer and for the negative mixing energy in cold water/ethanol trimers.

Spontaneous Raman scattering in supersonic jet expansions is used to prove that the mixed dimer of ethanol and water (corresponding to a volume fraction of 79% ethanol in the liquid) prefers ethanol in a gauche conformation as the hydrogen bond acceptor. This represents a particularly simple case of adaptive aggregation. Furthermore, it is shown experimentally that the isolated cold trimer built from one ethanol and two waters (corresponding to 64% ethanol in the liquid) has a significantly negative excess enthalpy, in line with the thermodynamic bulk observation at room temperature.

N-H...pi interactions in pyrroles: systematic trends from the vibrational spectroscopy of clusters.

Pyrrole and some of its methylated derivatives are aggregated in a controlled way in pulsed supersonic jet expansions. The cluster N-H stretching dynamics is studied using FTIR and Raman spectroscopy. Dimers, trimers and tetramers can be differentiated. Systematic trends in the dimer N-H...pi interaction as a function of methyl substitution are identified and explored for predictions. Overtone jet absorption spectroscopy is used to extract anharmonicities for the N-H bond in different environments. The N-H anharmonicity constant increases by 10% upon dimerization. Bulk matrix shifts can be emulated by the formation of Ar-decorated clusters. The experimental results are expected to serve as benchmarks for an accurate ab initio characterization of the N-H...pi hydrogen bond.

A peptide co-solvent under scrutiny: self-aggregation of 2,2,2-trifluoroethanol.

Trifluoroethanol (TFE) and its aggregates are studied via supersonic jet FTIR and Raman spectroscopy as well as by quantum chemistry and simple force field approaches. A multi-slit nozzle is introduced to study collisionally excited clusters. Efforts are made to extract harmonic frequencies from experiment for better comparison to theory. Based on deuteration, the OH stretching anharmonicity changes weakly upon dimerization, but increases for trimers. Among the possible dimer conformations, only an all-gauche, homoconfigurational, compact, OH-F connected structure is observed in an extreme case of chiral discrimination. Quantum tunneling assisted pathways for this surprising helicity synchronization are postulated. The oscillator coupling in hydrogen-bonded trimers is analyzed. Trans conformations of TFE start to become important for trimers and probably persist in the liquid state. Simple force fields can be refined to capture some molecular recognition features of TFE dimer, but their limitations are emphasized.

Structural preferences, argon nanocoating, and dimerization of n-alkanols as revealed by OH stretching spectroscopy in supersonic jets.

n-Alkanols can occur in a multitude of energetically competitive conformational states. Using the OH stretching vibration as an infrared and Raman spectroscopic sensor in supersonic jet expansions, the torsional preferences around the Calpha-O and Cbeta-Calpha bonds are probed for n-propanol through n-hexanol. Raman detection is more powerful for isolated monomers, whereas IR spectroscopy is more sensitive for molecular complexes. The subtle IR vibrational shift induced by the nanocoating of n-alcohols with Ar atoms is shown to alternate with chain length. A large number of alcohol dimer absorptions is observed and subjected to collisional relaxation and nanocoating conditions. Essential features of the dimer spectra are modeled successfully by a simple force field approach. Exploratory quantum chemical calculations up to the MP2/aug-cc-pvqz level encourage a rigorous theoretical study of the subtle conformational aspects in monomers and possibly also in dimers of linear alcohols.

Hydrogen-bonded OH stretching modes of methanol clusters: a combined IR and Raman isotopomer study.

A comprehensive study of the OH and OD stretching fundamentals in clusters of methanol and its isotopomers CH(3)OD, CD(3)OH, and CD(3)OD provides detailed insights into the hydrogen-bond mediated coupling as a function of cluster size. The combination of infrared and Raman supersonic jet spectroscopy enables the observation and assignment of all hydrogen-bonded OH stretching modes of isolated methanol trimer and methanol tetramer. A consistent explanation for the spectral complexity observed more than a decade ago in methanol trimer in terms of low-frequency methyl umbrella motions is provided. Previous explanations based on cluster isomerism or anharmonic resonances are ruled out by dedicated jet experiments. The first experimental lower bound for concerted quadruple proton transfer in S(4) symmetric methanol tetramer is derived and compared with theoretical predictions. The observed isotope effects offer insights into the anharmonicity of the localized OH bond. The performance of harmonic B3LYP and MP2 calculations in predicting hydrogen-bond-induced spectral shifts and couplings is investigated.

Concerted proton motion in hydrogen-bonded trimers: a spontaneous Raman scattering perspective.

Raman active symmetric O-H stretching modes are detected and assigned for the first time in isolated methanol, ethanol and methyl lactate trimers, providing insights into cluster structure, vibrational assignments and hydrogen-bond mediated couplings.