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Surface Lattice-Embedded Pt Single-Atom Catalyst on Ceria-Zirconia with Superior Catalytic Performance for Propane Oxidation.
Tan, Wei; Xie, Shaohua; Cai, Yandi; Yu, Haowei; Ye, Kailong; Wang, Meiyu; Diao, Weijian; Ma, Lu; Ehrlich, Steven N; Gao, Fei; Dong, Lin; Liu, Fudong.
Afiliação
  • Tan W; Department of Civil, Environmental, and Construction Engineering, Catalysis Cluster for Renewable Energy and Chemical Transformations (REACT), NanoScience Technology Center (NSTC), University of Central Florida, Orlando, Florida 32816, United States.
  • Xie S; State Key Laboratory of Pollution Control and Resource Reuse, School of Environment; Jiangsu Key Laboratory of Vehicle Emissions Control, Center of Modern Analysis; Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
  • Cai Y; Department of Civil, Environmental, and Construction Engineering, Catalysis Cluster for Renewable Energy and Chemical Transformations (REACT), NanoScience Technology Center (NSTC), University of Central Florida, Orlando, Florida 32816, United States.
  • Yu H; State Key Laboratory of Pollution Control and Resource Reuse, School of Environment; Jiangsu Key Laboratory of Vehicle Emissions Control, Center of Modern Analysis; Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
  • Ye K; State Key Laboratory of Pollution Control and Resource Reuse, School of Environment; Jiangsu Key Laboratory of Vehicle Emissions Control, Center of Modern Analysis; Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
  • Wang M; Department of Civil, Environmental, and Construction Engineering, Catalysis Cluster for Renewable Energy and Chemical Transformations (REACT), NanoScience Technology Center (NSTC), University of Central Florida, Orlando, Florida 32816, United States.
  • Diao W; College of Engineering and Applied Sciences, Nanjing University, Nanjing 210093, China.
  • Ma L; Department of Chemical and Biological Engineering, Villanova University, Villanova, Pennsylvania 19085, United States.
  • Ehrlich SN; National Synchrotron Light Source II (NSLS-II), Brookhaven National Laboratory, Upton, New York 11973, United States.
  • Gao F; National Synchrotron Light Source II (NSLS-II), Brookhaven National Laboratory, Upton, New York 11973, United States.
  • Dong L; State Key Laboratory of Pollution Control and Resource Reuse, School of Environment; Jiangsu Key Laboratory of Vehicle Emissions Control, Center of Modern Analysis; Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
  • Liu F; State Key Laboratory of Pollution Control and Resource Reuse, School of Environment; Jiangsu Key Laboratory of Vehicle Emissions Control, Center of Modern Analysis; Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
Environ Sci Technol ; 57(33): 12501-12512, 2023 08 22.
Article em En | MEDLINE | ID: mdl-37563957
Tuning the metal-support interaction and coordination environment of single-atom catalysts can help achieve satisfactory catalytic performance for targeted reactions. Herein, via the facile control of calcination temperatures for Pt catalysts on pre-stabilized Ce0.9Zr0.1O2 (CZO) support, Pt single atoms (Pt1) with different strengths of Pt-CeO2 interaction and coordination environment were successfully constructed. With the increase in calcination temperature from 350 to 750 °C, a stronger Pt-CeO2 interaction and higher Pt-O-Ce coordination number were achieved due to the reaction between PtOx and surface Ce3+ species as well as the migration of Pt1 into the surface lattice of CZO. The Pt/CZO catalyst calcined at 750 °C (Pt/CZO-750) exhibited a surprisingly higher C3H8 oxidation activity than that calcined at 550 °C (Pt/CZO-550). Through systematic characterizations and reaction mechanism study, it was revealed that the higher concentration of surface Ce3+ species/oxygen vacancies and the stronger Pt-CeO2 interaction on Pt/CZO-750 could better facilitate the activation of oxygen to oxidize C3H8 into reactive carbonate/carboxyl species and further promote the transformation of these intermediates into gaseous CO2. The Pt/CZO-750 catalyst can be a potential candidate for the catalytic removal of hydrocarbons from vehicle exhaust.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigênio / Propano Idioma: En Revista: Environ Sci Technol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigênio / Propano Idioma: En Revista: Environ Sci Technol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos