Response to Comment on “Active sites for CO 2 hydrogenation to methanol on Cu/ZnO catalysts”

Author:

Kattel Shyam1ORCID,Ramírez Pedro J.2ORCID,Chen Jingguang G.13ORCID,Rodriguez José A.14ORCID,Liu Ping14ORCID

Affiliation:

1. Chemistry Division, Brookhaven National Laboratory, Upton, NY 11973, USA.

2. Facultad de Ciencias, Universidad Central de Venezuela, Caracas 1020-A, Venezuela.

3. Department of Chemical Engineering, Columbia University, New York, NY 10027, USA.

4. Department of Chemistry, State University of New York–Stony Brook, Stony Brook, NY 11790, USA.

Abstract

In their Comment on the our recent Report, Nakamura et al . argue that our x-ray photoelectron spectroscopy (XPS) analysis was affected by the presence of formate species on the catalyst surface. This argument is not valid because the reactant gases were evacuated at temperatures from 525 to 575 kelvin, conditions under which formate is not stable on the catalyst surface. An analysis of the XPS results obtained after exposing zinc oxide/copper (111) [ZnO/Cu(111)] surfaces to hydrogen (H 2 ) and mixtures of carbon dioxide (CO 2 )/H 2 show an absence of carbon (C) 1s signal, no asymmetries in the oxygen (O) 1s peak, and a Zn:O intensity close to 1:1. Thus, the most active phase of these catalysts contained a ZnO-Cu interface.

Funder

US Department of Energy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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