6533b86ffe1ef96bd12ce812

RESEARCH PRODUCT

Pd nanoparticles formation inside porous polymeric scaffolds followed by in situ XANES/SAXS

Francesco GianniciAlessandro LongoWei LiuWei LiuAndrea LazzariniCarlo LambertiCarlo LambertiElisa BorfecchiaGiovanni AgostiniGiovanni AgostiniElena GroppoGiuseppe Portale

subject

HistoryMaterials scienceAbsorption spectroscopyNanoparticlechemistry.chemical_elementreduction02 engineering and technologypolystyrene010402 general chemistry01 natural sciencesEducationP4VPchemistry.chemical_compoundPdPd nanoparticles formation inside porous polymeric scaffoldspaladumchemistry.chemical_classification[PHYS]Physics [physics]Small-angle X-ray scatteringnanoparticlein situSAXS XANES Pd paladum nanoparticle polystyrene P4VP DRIFT TEM reduction in situSAXSPolymer021001 nanoscience & nanotechnologyXANESXANES0104 chemical sciencesComputer Science ApplicationsCrystallographyDRIFTchemistryChemical engineeringTEMPolystyreneDiffuse reflection0210 nano-technologyPalladium

description

International audience; Simultaneous time-resolved SAXS and XANES techniques were employed to follow in situ the formation of Pd nanoparticles from palladium acetate precursor in two porous polymeric supports: polystyrene (PS) and poly(4-vinyl-pyridine) (P4VP). In this study we have investigated the effect of the use of different reducing agents (H-2 and CO) from the gas phase. These results, in conjunction with data obtained by diffuse reflectance IR (DRIFT) spectroscopy and TEM measurements, allowed us to unravel the different roles played by gaseous H-2 and CO in the formation of the Pd nanoparticles for both PS and P4VP hosting scaffolds

10.1088/1742-6596/712/1/012039https://hal.archives-ouvertes.fr/hal-01572833/file/JPCS_712_012039.pdf