Superior CO Catalytic Oxidation on Novel Pt/Clay Nanocomposites
Source abstract
Abstract
Nanostructured novel Pt/Clay nanocomposites consisting of well-defined Pt nanoparticles prepared by clay-mediated in situ reduction displays very high thermal stability, large BET surface area and superior catalytic activity for CO oxidation as compared to a model reference Pt/SiO2 catalysts. CO oxidation has attracted renewed attention because of its technological importance in the area of pollution control. The Pt/Clay system consisting of Pt nanoparticles strongly immobilized between the atomic layers of clay inhibits nanoparticle sintering and loss of catalytic activity even after prolonged heating at high temperatures. At elevated temperatures (300 °C), the Pt/Clay system demonstrates significant enhancement of catalytic activity, with almost 100% CO conversion in less than 5 min. Emphasis is given to the role played by the clay supporting material which is chemically and thermally stable under the catalytic conditions of exhaust purification.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Catalysis and Oxidation Reactions · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Material Chemistry Laboratory, Kawamura Institute of Chemical Research, 631 Sakado, Sakura, Chiba 285-0078, Japan
National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan
Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan
References (31)
Show source-provided references
1. Norskov J. K. · Nat. Chem. · 2009 · 1 · 3710.1038/nchem.121 ↗
2. Chen A. · Chem. Rev. · 2010 · 110 · 376710.1021/cr9003902 ↗
3. Saravanan G. · Langmuir · 2010 · 26 · 1144610.1021/la100942h ↗
4. Behafarid F. · Nano Lett. · 2011 · 11 · 529010.1021/nl2027525 ↗
5. Heck R. M. · 200910.1002/9781118397749 ↗
6. Bowker M. · Chem. Soc. Rev. · 2008 · 37 · 220410.1039/b719206c ↗
7. Nishihata Y. · Nature · 2002 · 418 · 16410.1038/nature00893 ↗
8. Nagai Y. · R&D Rev. Toyota CRDL · 2011 · 42 · 43
9. Naitabdi A. · Appl. Phys. Lett. · 2009 · 94 · 08310210.1063/1.3083557 ↗
10. Mostafa S. · J. Am. Chem. Soc. · 2010 · 132 · 1571410.1021/ja106679z ↗
11. Leontyev I. N. · J. Phys. Chem. C · 2011 · 115 · 542910.1021/jp1109477 ↗
12. Hu N. F. · Anal. Chem. · 1991 · 63 · 216310.1021/ac00019a017 ↗
13. Macha S. M. · Mikrochim. Acta · 1998 · 128 · 110.1007/BF01242184 ↗
14. Zhou Y. L. · Langmuir · 2002 · 18 · 857310.1021/la026120x ↗
15. Van Olphen H. · 1977
16. Haraguchi K. · Adv. Mater. · 2006 · 18 · 225010.1002/adma.200600143 ↗
17. Haraguchi K. · Adv. Mater. · 2002 · 14 · 112010.1002/1521-4095(20020816)14:16<1120::AID-ADMA1120>3.0.CO;2-9 ↗
18. Datta K. K. R. · Chem. Commun. · 2010 · 46 · 61610.1039/B919421E ↗
19. Zhang R. · Langmuir · 2010 · 26 · 582310.1021/la903747v ↗
20. Burridge K. · J. Mater. Chem. · 2011 · 21 · 73410.1039/C0JM02702B ↗
21. Abdullayev E. · ACS Appl. Mater. Interfaces · 2011 · 3 · 404010.1021/am200896d ↗
22. Varadwaj G. B. V. · RSC Adv. · 2013 · 3 · 1358310.1039/c3ra40520f ↗
23. Varade D. · Langmuir · 2013 · 29 · 197710.1021/la3044945 ↗
24. Varade D. · Phys. Chem. Chem. Phys. · 2013 · 15 · 1647710.1039/c3cp52938j ↗
25. Bielamnski A. · 1991
26. Haraguchi K. · Macromolecules · 2005 · 38 · 348210.1021/ma047431c ↗
27. McClure S. M. · Catal. Lett. · 2009 · 133 · 29810.1007/s10562-009-0180-z ↗
28. Centeno M. A. · J. Mol. Catal. A: Chem. · 2006 · 252 · 14210.1016/j.molcata.2006.02.056 ↗
29. Ivanova S. · ChemCatChem · 2010 · 2 · 55610.1002/cctc.200900302 ↗
30. Gajan D. · J. Am. Chem. Soc. · 2009 · 131 · 1466710.1021/ja903730q ↗
31. Pina-Zapardiel R. · J. Nanopart. Res. · 2011 · 13 · 523910.1007/s11051-011-0508-7 ↗