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Details

Autor(en) / Beteiligte
Titel
Highly active and thermally stable single-atom catalysts for high-temperature electrochemical devices
Ist Teil von
  • Energy & environmental science, 2020-12, Vol.13 (12), p.493-492
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2020
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Single-atom catalysts provide unique catalytic properties and maximize the atom utilization efficiency. While utilizing them at elevated temperatures is highly desirable, their operating temperature is usually kept below 300 °C to prevent isolated atoms from agglomerating. Moreover, their applications in high-temperature electrochemical devices have been hindered by the lack of suitable processing techniques for catalyst loading. Herein, we report single-atom Pt/ceria nanocatalysts that are highly active and thermally stable in solid oxide cells (SOCs) operating at 600-800 °C. Our urea-based chemical solution process creates strong Pt-O-Ce interactions that securely anchor isolated Pt atoms to the surface of ceria nanoparticles and suppress their high-temperature migration. These single-atom Pt/ceria nanocatalysts are loaded in the oxide fuel electrode of a SOC via an in situ synthetic process, which reduces the polarization resistance from 28.2 to 0.82 Ohm cm 2 at 600 °C. This electrode outperforms the state-of-the-art Ni-based fuel electrode by up to 10 times and delivers extremely high performance in full SOCs in fuel cell and electrolysis modes. Furthermore, it stably operates at 700 °C for over 500 h under realistic operating conditions. Our results provide guidance to resolve the critical issues for the practical use of single-atom catalysts in various industrial processes and accelerate the commercial development of next-generation high-temperature energy devices. Single-atom Pt/ceria catalysts are extremely active and thermally stable at over 700 °C in high-temperature solid oxide cell electrodes.
Sprache
Englisch
Identifikatoren
ISSN: 1754-5692
eISSN: 1754-5706
DOI: 10.1039/d0ee01680b
Titel-ID: cdi_rsc_primary_d0ee01680b

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