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Octahedral palladium nanoparticles as excellent hosts for electrochemically adsorbed and absorbed hydrogen.


ABSTRACT: We report new results for electrochemical H adsorption on and absorption in octahedral palladium nanoparticles (Pd-NPs) with an average tip-to-tip size of 7.8 nm and a narrow size distribution. They reveal a very high H loading of 0.90 that cannot be achieved using bulk Pd materials or larger NPs; this behavior is assigned to a combination of two factors: their small size and face morphology. Temperature-dependent cyclic voltammetry (CV) studies in the range of 296 to 333 K reveal unique features that are attributed to electrochemical H adsorption, H absorption, and H2 generation. The CV features are used to prepare H adsorption and absorption isotherms that are then used in thermodynamic data analysis. Modeling of the experimental results demonstrates that, upon H adsorption and absorption, Pd-NPs develop a core-shell-skin structure, each with its unique H loading. The electrochemical results obtained for octahedral Pd-NPs are compared to analogous data obtained for cubic Pd-NPs with a similar size as well as for larger cubic Pd-NPs and bulk materials under gas-phase conditions.

SUBMITTER: Zalineeva A 

PROVIDER: S-EPMC5291700 | biostudies-other | 2017 Feb

REPOSITORIES: biostudies-other

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Octahedral palladium nanoparticles as excellent hosts for electrochemically adsorbed and absorbed hydrogen.

Zalineeva Anna A   Baranton Stève S   Coutanceau Christophe C   Jerkiewicz Gregory G  

Science advances 20170203 2


We report new results for electrochemical H adsorption on and absorption in octahedral palladium nanoparticles (Pd-NPs) with an average tip-to-tip size of 7.8 nm and a narrow size distribution. They reveal a very high H loading of 0.90 that cannot be achieved using bulk Pd materials or larger NPs; this behavior is assigned to a combination of two factors: their small size and face morphology. Temperature-dependent cyclic voltammetry (CV) studies in the range of 296 to 333 K reveal unique feature  ...[more]

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