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Issue 9, 2013
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Theoretical design and experimental implementation of Ag/Au electrodes for the electrochemical reduction of nitrate

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Abstract

The current imbalance in the biogeochemical cycle of nitrogen is as serious as that of carbon. One way to mitigate this problem is through the electrochemical reduction of nitrates under mild conditions, which is an appealing though not fully understood process. Therefore, deeper insight into the electrocatalytic reaction mechanism is needed to optimize this process. Here we thoroughly analyse the adsorption energy of nitrate with DFT calculations on various surface facets of pure Au, Ag, and their near-surface and surface alloys, as the adsorption and subsequent reduction of nitrate are thought to be rate limiting in the electrocatalytic reaction. The observed systematic trends allow prediction of the surface with highest electrocatalytic activity for the reduction of nitrate. This prediction was verified experimentally by depositing sub-monolayer amounts of Ag on polycrystalline Au electrodes. We observe a well-defined volcano curve which correlates the amount of Ag deposited on the surface with the current density at a fixed potential, with the peak activity around 2/3 ML Ag surface coverage. The electrocatalytic activity and stability of the bimetallic Ag–Au systems, found through the interplay of theoretical modelling and empirical observations, serve as a clear example for the rational design of novel catalytic materials and confirm the key role that the adsorption of nitrate plays in the overall nitrate reduction rate.

Graphical abstract: Theoretical design and experimental implementation of Ag/Au electrodes for the electrochemical reduction of nitrate

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Supplementary files

Article information


Submitted
02 Oct 2012
Accepted
20 Dec 2012
First published
21 Dec 2012

Phys. Chem. Chem. Phys., 2013,15, 3196-3202
Article type
Paper

Theoretical design and experimental implementation of Ag/Au electrodes for the electrochemical reduction of nitrate

F. Calle-Vallejo, M. Huang, J. B. Henry, M. T. M. Koper and A. S. Bandarenka, Phys. Chem. Chem. Phys., 2013, 15, 3196
DOI: 10.1039/C2CP44620K

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