In Situ Synthesis of Platinum Nanocatalysts on a Microstructured Paperlike Matrix for the Catalytic Purification of Exhaust Gases

The successful in situ synthesis of platinum nanoparticles (PtNPs) on a microstructured paperlike matrix, comprising ceramic fibers as main framework and zinc oxide whiskers as selective support for the PtNPs, is reported. The as‐prepared hybrid material (PtNPs@ZnO “paper”) resembles ordinary paper...

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Veröffentlicht in:ChemSusChem 2010-05, Vol.3 (5), p.604-608
Hauptverfasser: Koga, Hirotaka, Umemura, Yuuka, Tomoda, Akihiko, Suzuki, Ryo, Kitaoka, Takuya
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Sprache:eng
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Zusammenfassung:The successful in situ synthesis of platinum nanoparticles (PtNPs) on a microstructured paperlike matrix, comprising ceramic fibers as main framework and zinc oxide whiskers as selective support for the PtNPs, is reported. The as‐prepared hybrid material (PtNPs@ZnO “paper”) resembles ordinary paper products because it is flexible, lightweight, and easy to handle. In the catalytic reduction of nitrogen oxide (NOx) with propene for exhaust gas purification, the PtNPs@ZnO paper demonstrates a high catalytic performance at a low reaction temperature, with one‐third the dosage of precious platinum compared to conventional platinum‐loaded honeycomb catalysts. These results imply that the combination of easily synthesized PtNPs and a unique fiber‐network microstructure can provide excellent performances, promoting the effective transport of heat and reactants to the active sites of the platinum nanocatalysts. Thus, PtNPs@ZnO materials with paperlike practical aspects are promising catalytic materials for efficient NOx gas purification. Highly active platinum nanoparticles are prepared in situ on a microstructured “paper” matrix, using ceramic fibers as the main framework and ZnO whiskers as a selective support for the nanoparticles. The flexible PtNPs@ZnO paperlike material is convenient to handle and demonstrates an excellent catalytic performance for efficient NOx gas purification, having a higher efficiency at a lower reaction temperature compared to conventional Pt catalysts, with only one‐third of the Pt loading.
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.200900277