New Insights on the Nickel State Deposited by Hydrazine Wet-Chemical Synthesis Route in the Ni/BCY15 Proton-Conducting SOFC Anode.

Yttrium-doped barium cerate (BCY15) was used as an anode ceramic matrix for synthesis of the Ni-based cermet anode with application in proton-conducting solid oxide fuel cells (pSOFC). The hydrazine wet-chemical synthesis was developed as an alternative low-cost energy-efficient route that promotes 'in situ' introduction of metallic Ni particles in the BCY15 matrix. The focus of this study is a detailed comparative characterization of the nickel state in the Ni/BCY15 cermets obtained in two types of medium, aqueous and anhydrous ethylene glycol environment, performed by a combination of XRD, N physisorption, SEM, EPR, XPS, and electrochemical impedance spectroscopy.

Oxygen-Storage Materials to Stabilize the Oxygen Redox Activity of Three-Layered Sodium Transition Metal Oxides.

To double the energy density of lithium- and sodium-ion batteries there is a need to activate simultaneously cationic and anionic redox reactions at the intercalation-type electrodes. In contrast to the cationic redox activity, the oxygen redox activity enforces an enhancement in the surface reactivity of the oxides leading to their poor reversibility and cycling stability. Herein, we propose a new concept to stabilize oxygen redox activity by using oxygen-storage materials as an efficient buffer supplying and receiving oxygen during alkali ion intercalation.

Mesoporous alumina from colloidal biotemplating of Al clusters.

A simple and green synthesis route was disclosed for the achievement of mesoporous alumina microparticles employing polysaccharide nanoparticles (α-chitin nanorods) as templates. Pore textures can be tuned by the cationic alumina precursor. Compared to small cations, the use of Al13 and Al30 oxo-hydroxo clusters leads to better defined and elongated mesopores.

Theoretical and experimental local reactivity parameters of 3-substituted coumarin derivatives.

Local reactivity descriptors, such as atomic charges, atomic electrostatic potential and atomic Fukui indices were computed for a series of 3-substituted coumarin (2-oxo-2H-1-benzopyran) derivatives, using density functional theory (DFT) and Möller-Plesset methods (MP2). The variation of those properties as a function of the substituents was compared with the variation of the measured XPS binding energies. The atomic electrostatic potentials and XPS binding energies serves as indicators of the electrophilicity of a given center within a molecule, while the atomic Fukui indices describe its degree of electronic localization, known as atomic softness.

Ultrafast charge transfer at monolayer graphene surfaces with varied substrate coupling.

The charge transfer rates of a localized excited electron to graphene monolayers with variable substrate coupling have been investigated by the core hole clock method with adsorbed argon. Expressed as charge transfer times, we find strong variations between ~3 fs (on graphene "valleys" on Ru(0001)) to ~16 fs (quasi-free graphene on SiC, O/Ru(0001), or SiO2/Ru). The values for the "hills" on Gr/Ru and on Gr/Pt(111) are in between, with the ratio 1.

Vibrational characterization of ethylene adsorption and its thermal evolution on Si(001)-(2 x 1): identification of majority and minority species.

The vibrational and structural properties of a single-domain Si(001)-(2 x 1) surface upon ethylene adsorption have been studied by density functional cluster calculations and high-resolution electron energy loss spectroscopy. The detailed analysis of the theoretically and the experimentally determined vibrational frequencies reveals two coexisting adsorbate configurations. The majority species consist of ethylene molecules which are di-sigma bonded to the two Si atoms of a single Si-Si dimer.