Effect of complex oxide promoters and Pd on activity and stability of Ni/YSZ (ScSZ) cermets as anode materials for IT SOFC

Effect of fluorite-like or perovskite-like complex oxide promoters, Pd and Cu on the performance of Ni/8YSZ and Ni/ScCeSZ anode materials in CH4 steam reforming (SR) or selective oxidation (SO) by O-2 into syngas was studied. The spatial distribution of dopants in composites before and after contact with the reaction feed, features of components mutual interaction and forms of deposited coke were controlled by TEM combined with EDX analysis. The lattice oxygen mobility and reactivity were estimated by CH4 and H-2 temperature-programmed reduction (TPR), and the amount of deposited carbon after operation in the feed with stoichiometric H2O/CH4 ratio was estimated by the temperature-programmed oxidation. Promoters decrease the amount of deposited coke, while doping by Pd or Cu ensures also a good and stable performance at moderate (similar to 550 degrees C) temperatures required for the intermediate-temperature solid oxide fuel cells (IT SOFC) operation. (c) 2007 Elsevier B.V. All rights reserved.</p

Structural basis for selectivity and diversity in angiotensin II receptors

The angiotensin II receptors AT1R and AT2R serve as key components of the renin–angiotensin–aldosterone system. AT1R has a central role in the regulation of blood pressure, but the function of AT2R is unclear and it has a variety of reported effects. To identify the mechanisms that underlie the differences in function and ligand selectivity between these receptors, here we report crystal structures of human AT2R bound to an AT2R-selective ligand and to an AT1R/AT2R dual ligand, capturing the receptor in an active-like conformation. Unexpectedly, helix VIII was found in a non-canonical position, stabilizing the active-like state, but at the same time preventing the recruitment of G proteins or β-arrestins, in agreement with the lack of signalling responses in standard cellular assays. Structure–activity relationship, docking and mutagenesis studies revealed the crucial interactions for ligand binding and selectivity. Our results thus provide insights into the structural basis of the distinct functions of the angiotensin receptors, and may guide the design of newselective ligands