Your browser doesn't support javascript.
loading
Bridging Thermal Catalysis and Electrocatalysis: Catalyzing CO2 Conversion with Carbon-Based Materials.
Koshy, David M; Nathan, Sindhu S; Asundi, Arun S; Abdellah, Ahmed M; Dull, Samuel M; Cullen, David A; Higgins, Drew; Bao, Zhenan; Bent, Stacey F; Jaramillo, Thomas F.
Afiliação
  • Koshy DM; Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, CA, 94305, USA.
  • Nathan SS; SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Rd., Menlo Park, CA, 94025, USA.
  • Asundi AS; Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, CA, 94305, USA.
  • Abdellah AM; SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Rd., Menlo Park, CA, 94025, USA.
  • Dull SM; Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, CA, 94305, USA.
  • Cullen DA; SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Rd., Menlo Park, CA, 94025, USA.
  • Higgins D; Department of Chemical Engineering, McMaster University, 1280 Main St W, Hamilton, ON, L8S 4L8, Canada.
  • Bao Z; Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, CA, 94305, USA.
  • Bent SF; Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, 1 Bethel Valley Rd, Oak Ridge, TN, 37830, USA.
  • Jaramillo TF; Department of Chemical Engineering, McMaster University, 1280 Main St W, Hamilton, ON, L8S 4L8, Canada.
Angew Chem Int Ed Engl ; 60(32): 17472-17480, 2021 Aug 02.
Article em En | MEDLINE | ID: mdl-33823079
ABSTRACT
Understanding the differences between reactions driven by elevated temperature or electric potential remains challenging, largely due to materials incompatibilities between thermal catalytic and electrocatalytic environments. We show that Ni, N-doped carbon (NiPACN), an electrocatalyst for the reduction of CO2 to CO (CO2 R), can also selectively catalyze thermal CO2 to CO via the reverse water gas shift (RWGS) representing a direct analogy between catalytic phenomena across the two reaction environments. Advanced characterization techniques reveal that NiPACN likely facilitates RWGS on dispersed Ni sites in agreement with CO2 R active site studies. Finally, we construct a generalized reaction driving-force that includes temperature and potential and suggest that NiPACN could facilitate faster kinetics in CO2 R relative to RWGS due to lower intrinsic barriers. This report motivates further studies that quantitatively link catalytic phenomena across disparate reaction environments.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article