Colloidal Syntheses of Shape- and Size-Controlled Pt Nanoparticles for Electrocatalysis

International audienceDifferent colloidal synthesis methods of platinum nanoparticles with controlled sizes and shapes that are relevant for electrocatalysis studies are reviewed. Four main methods, i.e., water in oil microemulsion (w/o) method, polyacrylate (PA) method, tetradecyltrimethylammonium bromide (TTAB) method, and ethylene glycol method, are used to synthesize platinum nanoparticles. The PA method allowed us to synthesize reproducibly nanocubes, nanooctahedrons, or nanocuboctahedrons/truncated nanooctahedrons with size between 8 and 10 nm, the TTAB method led to the synthesis of nanocubes of about 10 nm, and the w/o method allowed the synthesis of spherical particles of about 3 nm. All these samples could be cleaned for further electrochemical characterization of their surface structure by hydrogen underpotential deposition and by spontaneous deposition and oxidation of bismuth and germanium, leading to a quantitative determination of the (100) and (111) surface domains. The samples prepared by the ethylene glycol method, in the presence or not of polyvinylpyrrolydone as surfactant, were size or shape controlled, but did not allow the electrochemical characterization of their surface due to remaining of strongly adsorbed organic species even after cleaning steps

New findings on CO electrooxidation at platinum nanoparticle surfaces

Different unsupported platinum nanoparticles are synthesized via water-in-oil microemulsion and colloidal methods (PAA). TEM, adatom adsorption and cyclic voltammetry measurements give very coherent results concerning the surface structure of the crystallites. The combination of these results with CO stripping experiments leads us to assign the oxidation peak multiplicity to surface structure rather than to pure size effect. Keywords: Oriented platinum nanoparticles, CO electrooxidation, Cyclic voltammetr

A highly diverse siliceous sponge fauna (Porifera: Hexactinellida, Demospongiae) from the Eocene of north-eastern Italy: systematics and palaeoecology

A siliceous sponge fauna, consisting of more than 900 specimens, is described from an early Lutetian tuffite horizon in the Chiampo Valley, Lessini Mountains, north-eastern Italy. Thirty-two taxa (15 Hexactinellida, 17 Demospongiae) are determined and illustrated, belonging to 24 genera, two of which are new (Rigonia gen. nov. and Coronispongia gen. nov.). Among these, 10 new species are proposed: Stauractinella eocenica sp. nov., Rigonia plicata gen. et sp. nov., Hexactinella clampensis sp. nov., Camerospongia visentinae sp. nov., C. tuberculata sp. nov., Toulminia italica sp. nov., Coronispongia confossa gen. et sp. nov., Cavispongia scarpai sp. nov., Corallistes multiosculata sp. nov. and Bolidium bertii sp. nov. Of the genera identified at Chiampo, 14 range back to the Cretaceous, three to the Jurassic and one to the Triassic, while six are still extant. The studied fauna shows affinities with sponges from the Eocene of Spain and the Cretaceous of Germany. The sponge fossils are uncompressed and bodily preserved, but the original siliceous skeleton is dissolved and substituted by calcite. Delicate attachments can be nevertheless documented: some sponges attached to a hard substrate by encrustation, while others were anchored on soft sediments by root-like structures. The presence of different modes of attachment suggests heterogeneous substrate conditions. Small, possibly young, sponges are recorded too. The sponge fauna is essentially autochthonous and lived in the middle-outer part of a carbonate ramp, where it formed clusters. This study extends the geographical and stratigraphical range of many sponge taxa, including Camerospongia, Toulminia, Ozotrachelus and Bolidium, previously documented only from the Cretaceous. The Recent calcified demosponge genus Astrosclera is reported here in the Cenozoic for the first time, having been reported previously in the Triassic only. Additionally, this study documents the second worldwide occurrence of the Recent sphinctozoan genus Vaceletia in the Palaeogene, formerly recorded exclusively in Australia. http://zoobank.org/urn:lsid:zoobank.org:pub:B3466955-8E20-429A-89BE-42BAEB4002E8 \ua9 2016, \ua9 The Trustees of the Natural History Museum, London 2016. All Rights Reserved

Pt Particles Functionalized on the Molecular Level as New Nanocomposite Materials for Electrocatalysis

International audienceA nanocomposite material consisting of platinum nanoparticles surrounded by an ionic conducting polymer dispersed on carbon Vulcan XC72 was synthesized. The aim of this nanocomposite material is to translate the triple-phase boundary to a molecular level in electrochemical systems involving a polymer electrolyte. The ionic conducting polymer is a poly(styrenesulfonic acid) (PSSA, or PSSNa in its sodium form) synthesized by atom-transfer radical polymerization. The polymer has a terminal thiol group to ensure bonding with platinum nanoparticles. The nanocomposite material (Pt-PSSA/C) exhibited thermal stability up to 160 degrees C and electrochemical stability up to 1 V versus RI-LE. Compared to a Pt/C catalyst, the nanocomposite catalyst has a lower active surface area but comparable catalytic activity for the oxygen reduction reaction. Furthermore, this nanocomposite material exhibits similar behavior in a fuel cell active layer without Nafion as a classical Pt/C catalyst with Nafion included in the active layer