Initial Steps in Forming the Electrode–Electrolyte Interface: H2O Adsorption and Complex Formation on the Ag(111) Surface from Combining Quantum Mechanics Calculations and Ambient Pressure X-ray Photoelectron Spectroscopy-Reference-Cited by-同舟云学术

Initial Steps in Forming the Electrode–Electrolyte Interface: H2O Adsorption and Complex Formation on the Ag(111) Surface from Combining Quantum Mechanics Calculations and Ambient Pressure X-ray Photoelectron Spectroscopy

Published:2019-04-04 Issue:17 Volume:141 Page:6946-6954
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Qian Jin¹²^ORCID,Ye Yifan³⁴⁵,Yang Hao²,Yano Junko³^ORCID,Crumlin Ethan J.⁴⁵^ORCID,Goddard William A.¹²^ORCID

Affiliation:

1. Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, California 91125, United States

2. Materials and Process Simulation Center, California Institute of Technology, Pasadena, California 91125, United States

3. Joint Center for Artificial Photosynthesis, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

4. Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

5. Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

Funder

Basic Energy Sciences

Office of Science

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.8b13672

Reference40 articles.

1. Subsurface oxide plays a critical role in CO 2 activation by Cu(111) surfaces to form chemisorbed CO 2 , the first step in reduction of CO 2

2. Mechanistic Explanation of the pH Dependence and Onset Potentials for Hydrocarbon Products from Electrochemical Reduction of CO on Cu (111)

3. Significant difference of the reduction rates of carbon dioxide between Pt(111) and Pt(110) single crystal electrodes

4. Ag–Sn Bimetallic Catalyst with a Core–Shell Structure for CO2 Reduction

5. Predicted Structures of the Active Sites Responsible for the Improved Reduction of Carbon Dioxide by Gold Nanoparticles

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