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Details

Autor(en) / Beteiligte
Titel
Epitaxial growth of Pt–Pd bimetallic heterostructures for the oxygen reduction reaction
Ist Teil von
  • Advanced Powder Materials, 2023-10, Vol.2 (4), p.100131, Article 100131
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2023
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • It is of great importance to design highly active and stable electrocatalysts with low Pt loading to improve the sluggish kinetics of oxygen reduction reaction (ORR) for fuel cells. Herein, we report an epitaxial growth of a Pt–Pd bimetallic heterostructure with a Pt loading as low as 8.02 ​wt%. Both experimental studies and theoretical calculations confirm that the heterointerfaces play a major role in charge redistribution, which accelerates electron transfer from Pd to Pt, contributing to downshifting the d-band center of Pd and consequently greatly weakening the O adsorption energy for a critical optimal adsorption configuration of O∗ on the heterointerface. In particular, the adsorbed O∗, an intermediate in a bridge mode between adjacent Pt and Pd atoms, has a relative low adsorption energy, which easily forms H2O to escape for releasing the active sites toward ORR. The Pt–Pd heterostructured catalyst presents the highest mass activity of 6.06 A·mg−1Pt among all reported Pt–Pd alloyed or composited catalysts, which is 26.4 times of the sample Pt/C (0.23 A·mg−1Pt). Further, the fuel cell assembled by the electrocatalyst shows a current density of 1.23 ​A·cm−2 at 0.6 ​V and good stability for over 100 ​h. Epitaxial growth of Pt–Pd bimetallic heterostructure (Pt–Pd BHs) with a Pt loading as low as 8.02 ​wt% is achieved, and the obtained Pt–Pd BHs show highly enhanced ORR catalytic activity compared to Pt/C. The adsorption of O∗ in bridge mode between adjacent Pt and Pd atoms with a low adsorption energy originating from the charge redistribution in heterointerface regions enables the activity enhancement. [Display omitted]
Sprache
Englisch
Identifikatoren
ISSN: 2772-834X
eISSN: 2772-834X
DOI: 10.1016/j.apmate.2023.100131
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_d952e29adafe47ef9459ac4e866cbb9a

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