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Title: Mechanistic insights into electrochemical reduction of CO 2 over Ag using density functional theory and transport models

Abstract

Electrochemical reduction of CO 2 using renewable sources of electrical energy holds promise for converting CO 2 to fuels and chemicals. Since this process is complex and involves a large number of species and physical phenomena, a comprehensive understanding of the factors controlling product distribution is required. While the most plausible reaction pathway is usually identified from quantum-chemical calculation of the lowest free-energy pathway, this approach can be misleading when coverages of adsorbed species determined for alternative mechanism differ significantly, since elementary reaction rates depend on the product of the rate coefficient and the coverage of species involved in the reaction. Moreover, cathode polarization can influence the kinetics of CO 2 reduction. Here, we present a multiscale framework for ab initio simulation of the electrochemical reduction of CO 2 over an Ag(110) surface. A continuum model for species transport is combined with a microkinetic model for the cathode reaction dynamics. Free energies of activation for all elementary reactions are determined from density functional theory calculations. Using this approach, three alternative mechanisms for CO 2 reduction were examined. The rate-limiting step in each mechanism is **COOH formation at higher negative potentials. However, only via the multiscale simulation was it possible tomore » identify the mechanism that leads to a dependence of the rate of CO formation on the partial pressure of CO 2 that is consistent with experiments. Simulations based on this mechanism also describe the dependence of the H 2 and CO current densities on cathode voltage that are in strikingly good agreement with experimental observation.« less

Authors:
ORCiD logo; ; ; ORCiD logo; ORCiD logo
Publication Date:
Research Org.:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
OSTI Identifier:
1396063
Alternate Identifier(s):
OSTI ID: 1426740
Grant/Contract Number:  
SC0004993; AC02-05CH11231
Resource Type:
Published Article
Journal Name:
Proceedings of the National Academy of Sciences of the United States of America
Additional Journal Information:
Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Volume: 114 Journal Issue: 42; Journal ID: ISSN 0027-8424
Publisher:
Proceedings of the National Academy of Sciences
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; CO2 reduction; electrocatalysis; mechanism; density functional theory; transport model

Citation Formats

Singh, Meenesh R., Goodpaster, Jason D., Weber, Adam Z., Head-Gordon, Martin, and Bell, Alexis T. Mechanistic insights into electrochemical reduction of CO 2 over Ag using density functional theory and transport models. United States: N. p., 2017. Web. doi:10.1073/pnas.1713164114.
Singh, Meenesh R., Goodpaster, Jason D., Weber, Adam Z., Head-Gordon, Martin, & Bell, Alexis T. Mechanistic insights into electrochemical reduction of CO 2 over Ag using density functional theory and transport models. United States. doi:10.1073/pnas.1713164114.
Singh, Meenesh R., Goodpaster, Jason D., Weber, Adam Z., Head-Gordon, Martin, and Bell, Alexis T. Mon . "Mechanistic insights into electrochemical reduction of CO 2 over Ag using density functional theory and transport models". United States. doi:10.1073/pnas.1713164114.
@article{osti_1396063,
title = {Mechanistic insights into electrochemical reduction of CO 2 over Ag using density functional theory and transport models},
author = {Singh, Meenesh R. and Goodpaster, Jason D. and Weber, Adam Z. and Head-Gordon, Martin and Bell, Alexis T.},
abstractNote = {Electrochemical reduction of CO 2 using renewable sources of electrical energy holds promise for converting CO 2 to fuels and chemicals. Since this process is complex and involves a large number of species and physical phenomena, a comprehensive understanding of the factors controlling product distribution is required. While the most plausible reaction pathway is usually identified from quantum-chemical calculation of the lowest free-energy pathway, this approach can be misleading when coverages of adsorbed species determined for alternative mechanism differ significantly, since elementary reaction rates depend on the product of the rate coefficient and the coverage of species involved in the reaction. Moreover, cathode polarization can influence the kinetics of CO 2 reduction. Here, we present a multiscale framework for ab initio simulation of the electrochemical reduction of CO 2 over an Ag(110) surface. A continuum model for species transport is combined with a microkinetic model for the cathode reaction dynamics. Free energies of activation for all elementary reactions are determined from density functional theory calculations. Using this approach, three alternative mechanisms for CO 2 reduction were examined. The rate-limiting step in each mechanism is **COOH formation at higher negative potentials. However, only via the multiscale simulation was it possible to identify the mechanism that leads to a dependence of the rate of CO formation on the partial pressure of CO 2 that is consistent with experiments. Simulations based on this mechanism also describe the dependence of the H 2 and CO current densities on cathode voltage that are in strikingly good agreement with experimental observation.},
doi = {10.1073/pnas.1713164114},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
number = 42,
volume = 114,
place = {United States},
year = {2017},
month = {10}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
DOI: 10.1073/pnas.1713164114

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Cited by: 25 works
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    Works referencing / citing this record:

    Structure‐Sensitivity and Electrolyte Effects in CO 2 Electroreduction: From Model Studies to Applications
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