On the nature of the interaction of H2PdCl4 with the surface of graphite-like carbon materials
β Scribed by P.A. Simonov; A.V. Romanenko; I.P. Prosvirin; E.M. Moroz; A.I. Boronin; A.L. Chuvilin; V.A. Likholobov
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 1006 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0008-6223
No coin nor oath required. For personal study only.
β¦ Synopsis
Adsorption of H,PdCl,
from aqueous solutions on the surface of graphite-like carbon materials proceeds through two competitive pathways: reduction, which gives rise to Pd' particles of 6-100 nm in size, and formation of n-complexes of PdCl, with >C=C< fragments of the carbon matrix:
Process (1) is localized near the exterior surface of the porous carbon particles. Process (2) takes place on the whole surface of these particles. The quantitative ratio of the adsorbed palladium species (Pd'+ and Pd') and also the dispersion and morphology of the metallic particles depend on the mode of contact of the H,PdCl, solution with the carbon, the composition of the gas phase, the size of the carbon particles, the chemical state of the carbon surface and the conditions of drying. The results obtained are explained in terms of the electrochemical theory of carbon reactivity.
π SIMILAR VOLUMES
We ealenlate the interaction betv.een a II-. moIecuIe and a metal surface, represented by rs = 2 jellium. usinS the Cordon-Kim method\_ The adsorption curres for Ha p;trleI and perpendicular to the surface are presented, and analyzed using an indePendent-atom effectire potential. The molecular poten
Reversible electrochemical intercalation of unsolvated lithium into graphite previously treated either in LiClO,ethylene carbonate (EC) or in LiClO,-dimethyl carbonate (DMC) solutions was carried out in a LiClO,-propylene carbonate (PC) electrolyte. Under these conditions, graphite exfoliation did n