Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Quick Search
My eDoc
Session History
Support Wiki
Direct access to
document ID:

          Institute: MPI für bioanorganische Chemie     Collection: MPI für bioanorganische Chemie     Display Documents

ID: 697857.0, MPI für bioanorganische Chemie / MPI für bioanorganische Chemie
Dynamics of Palladium on Nanocarbon in the Direct Synthesis of H2O2
Authors:Arrigo, Rosa; Schuster, Manfred E.; Abate, Salvatore; Wrabetz, Sabine; Amakawa, Kazuhiko; Teschner, Detre; Freni, Maria; Centi, Gabriele; Perathoner, Siglinda; Hävecker, Michael; Schlögl, Robert
Date of Publication (YYYY-MM-DD):2014
Title of Journal:ChemSusChem
Issue / Number:1
Start Page:179
End Page:194
Review Status:Peer-review
Audience:Experts Only
Abstract / Description:This work aims to clarify the nanostructural transformation accompanying the loss of activity and selectivity for the hydrogen peroxide synthesis of palladium and gold-palladium nanoparticles supported on N-functionalized carbon nanotubes. High-resolution X-ray photoemission spectroscopy (XPS) allows the discrimination of metallic palladium, electronically modified metallic palladium hosting impurities, and cationic palladium. This is paralleled by the morphological heterogeneity observed by high-resolution TEM, in which nanoparticles with an average size of 2 nm coexisted with very small palladium clusters. The morphological distribution of palladium is modified after reaction through sintering and dissolution/redeposition pathways. The loss of selectivity is correlated to the extent to which these processes occur as a result of the instability of the particle at the carbon surface. We assign beneficial activity in the selective hydrogenation of oxygen to palladium clusters with a modified electronic structure compared with palladium metal or palladium oxides. These beneficial species are formed and stabilized on carbons modified with nitrogen atoms in substitutional positions. The formation of larger metallic palladium particles not only reduces the number of active sites for the synthesis, but also enhances the activity for deep hydrogenation to water. The structural instability of the active species is thus detrimental in a dual way. Minimizing the chance of sintering of palladium clusters by all means is thus the key to better performing catalysts.
External Publication Status:published
Document Type:Article
Communicated by:N. N.
Affiliations:MPI für bioanorganische Chemie
External Affiliations:[Arrigo,R.;Schuster,M. E.;Wrabetz, S.;Amakawa,K.; Teschner,D.; Schlögl,R.]Anorganische Chemie, Fritz-Haber-Institut der Max-Planck Gesellschaft, Germany;
[Abate,S.; Centi,G.; Perathoner,S.] Dipartimento di Chimica industriale Universita degli Studi di Messina,F.Stagnole D’Alcontres 31, 98166 Messina ,Italy;
[Hävecker,M.]Faradayweg 4-6, 14195 Berlin,Germany;
Identifiers:ISI:000336802400022 [ID No:1]
ISSN:1864-5631 [ID No:2]
DOI:10.1002/cssc.201300616 [ID No:3]
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.