Your browser doesn't support javascript.
loading
Photoinduced Strong Metal-Support Interaction for Enhanced Catalysis.
Chen, Hao; Yang, Zhenzhen; Wang, Xiang; Polo-Garzon, Felipe; Halstenberg, Phillip W; Wang, Tao; Suo, Xian; Yang, Shi-Ze; Meyer, Harry M; Wu, Zili; Dai, Sheng.
Afiliação
  • Chen H; Department of Chemistry, The University of Tennessee, Knoxville, Tennessee 37996, United States.
  • Yang Z; Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
  • Wang X; Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
  • Polo-Garzon F; Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
  • Halstenberg PW; Department of Chemistry, The University of Tennessee, Knoxville, Tennessee 37996, United States.
  • Wang T; Department of Chemistry, The University of Tennessee, Knoxville, Tennessee 37996, United States.
  • Suo X; Department of Chemistry, The University of Tennessee, Knoxville, Tennessee 37996, United States.
  • Yang SZ; Eyring Materials Center, Arizona State University, Tempe, Arizona 85287, United States.
  • Meyer HM; Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
  • Wu Z; Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
  • Dai S; Department of Chemistry, The University of Tennessee, Knoxville, Tennessee 37996, United States.
J Am Chem Soc ; 143(23): 8521-8526, 2021 Jun 16.
Article em En | MEDLINE | ID: mdl-34081447
ABSTRACT
Strong metal-support interaction (SMSI) construction is a pivotal strategy to afford thermally robust nanocatalysts in industrial catalysis, but thermally induced reactions (>300 °C) in specific gaseous atmospheres are generally required in traditional procedures. In this work, a photochemistry-driven methodology was demonstrated for SMSI construction under ambient conditions. Encapsulation of Pd nanoparticles with a TiOx overlayer, the presence of Ti3+ species, and suppression of CO adsorption were achieved upon UV irradiation. The key lies in the generation of separated photoinduced reductive electrons (e-) and oxidative holes (h+), which subsequently trigger the formation of Ti3+ species/oxygen vacancies (Ov) and then interfacial Pd-Ov-Ti3+ sites, affording a Pd/TiO2 SMSI with enhanced catalytic hydrogenation efficiency. The as-constructed SMSI layer was reversible, and the photodriven procedure could be extended to Pd/ZnO and Pt/TiO2.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos