Identification of active sites in CO oxidation and water-gas shift over supported Pt catalysts

Identification and characterization of catalytic active sites are the prerequisites for an atomic-level understanding of the catalytic mechanism and rational design of high-performance heterogeneous catalysts. Indirect evidence in recent reports suggests that platinum (Pt) single atoms are exception...

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Vydané v:Science (American Association for the Advancement of Science) Ročník 350; číslo 6257; s. 189
Hlavní autori: Ding, Kunlun, Gulec, Ahmet, Johnson, Alexis M, Schweitzer, Neil M, Stucky, Galen D, Marks, Laurence D, Stair, Peter C
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 09.10.2015
ISSN:1095-9203, 1095-9203
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Abstract Identification and characterization of catalytic active sites are the prerequisites for an atomic-level understanding of the catalytic mechanism and rational design of high-performance heterogeneous catalysts. Indirect evidence in recent reports suggests that platinum (Pt) single atoms are exceptionally active catalytic sites. We demonstrate that infrared spectroscopy can be a fast and convenient characterization method with which to directly distinguish and quantify Pt single atoms from nanoparticles. In addition, we directly observe that only Pt nanoparticles show activity for carbon monoxide (CO) oxidation and water-gas shift at low temperatures, whereas Pt single atoms behave as spectators. The lack of catalytic activity of Pt single atoms can be partly attributed to the strong binding of CO molecules.
AbstractList Identification and characterization of catalytic active sites are the prerequisites for an atomic-level understanding of the catalytic mechanism and rational design of high-performance heterogeneous catalysts. Indirect evidence in recent reports suggests that platinum (Pt) single atoms are exceptionally active catalytic sites. We demonstrate that infrared spectroscopy can be a fast and convenient characterization method with which to directly distinguish and quantify Pt single atoms from nanoparticles. In addition, we directly observe that only Pt nanoparticles show activity for carbon monoxide (CO) oxidation and water-gas shift at low temperatures, whereas Pt single atoms behave as spectators. The lack of catalytic activity of Pt single atoms can be partly attributed to the strong binding of CO molecules.Identification and characterization of catalytic active sites are the prerequisites for an atomic-level understanding of the catalytic mechanism and rational design of high-performance heterogeneous catalysts. Indirect evidence in recent reports suggests that platinum (Pt) single atoms are exceptionally active catalytic sites. We demonstrate that infrared spectroscopy can be a fast and convenient characterization method with which to directly distinguish and quantify Pt single atoms from nanoparticles. In addition, we directly observe that only Pt nanoparticles show activity for carbon monoxide (CO) oxidation and water-gas shift at low temperatures, whereas Pt single atoms behave as spectators. The lack of catalytic activity of Pt single atoms can be partly attributed to the strong binding of CO molecules.
Identification and characterization of catalytic active sites are the prerequisites for an atomic-level understanding of the catalytic mechanism and rational design of high-performance heterogeneous catalysts. Indirect evidence in recent reports suggests that platinum (Pt) single atoms are exceptionally active catalytic sites. We demonstrate that infrared spectroscopy can be a fast and convenient characterization method with which to directly distinguish and quantify Pt single atoms from nanoparticles. In addition, we directly observe that only Pt nanoparticles show activity for carbon monoxide (CO) oxidation and water-gas shift at low temperatures, whereas Pt single atoms behave as spectators. The lack of catalytic activity of Pt single atoms can be partly attributed to the strong binding of CO molecules.
Author Johnson, Alexis M
Schweitzer, Neil M
Stucky, Galen D
Gulec, Ahmet
Marks, Laurence D
Ding, Kunlun
Stair, Peter C
Author_xml – sequence: 1
  givenname: Kunlun
  surname: Ding
  fullname: Ding, Kunlun
  organization: Department of Chemistry, Northwestern University, Evanston, IL 60208, USA
– sequence: 2
  givenname: Ahmet
  surname: Gulec
  fullname: Gulec, Ahmet
  organization: Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA
– sequence: 3
  givenname: Alexis M
  surname: Johnson
  fullname: Johnson, Alexis M
  organization: Department of Chemistry, Northwestern University, Evanston, IL 60208, USA
– sequence: 4
  givenname: Neil M
  surname: Schweitzer
  fullname: Schweitzer, Neil M
  organization: Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA
– sequence: 5
  givenname: Galen D
  surname: Stucky
  fullname: Stucky, Galen D
  organization: Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106, USA
– sequence: 6
  givenname: Laurence D
  surname: Marks
  fullname: Marks, Laurence D
  organization: Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA
– sequence: 7
  givenname: Peter C
  surname: Stair
  fullname: Stair, Peter C
  email: pstair@northwestern.edu
  organization: Department of Chemistry, Northwestern University, Evanston, IL 60208, USA. Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, IL 60439, USA. pstair@northwestern.edu
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26338796$$D View this record in MEDLINE/PubMed
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