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Phys Chem Chem Phys. 2016 Apr 14;18(14):9652-7. doi: 10.1039/c6cp00542j. Epub 2016 Mar 21.

On the mechanism of high product selectivity for HCOOH using Pb in CO2 electroreduction.

Author information

1
Graduate School of EEWS, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehakro, Daejeon 305-701, Korea. ysjn@kaist.ac.kr.

Abstract

While achieving high product selectivity is one of the major challenges of the CO2 electroreduction technology in general, Pb is one of the few examples with high selectivity that produces formic acid almost exclusively (versus H2, CO, or other byproducts). In this work, we study the mechanism of CO2 electroreduction reactions using Pb to understand the origin of high formic acid selectivity. In particular, we first assess the proton-assisted mechanism proposed in the literature using density functional calculations and find that it cannot fully explain the previous selectivity experiments for the Pb electrode. We then suggest an alternative proton-coupled-electron-transfer mechanism consistent with existing observations, and further validate a new mechanism by experimentally measuring and comparing the onset potentials for CO2 reduction vs. H2 production. We find that the origin of a high selectivity of the Pb catalyst for HCOOH production over CO and H2 lies in the strong O-affinitive and weak C-, H-affinitive characteristics of Pb, leading to the involvement of the *OCHO species as a key intermediate to produce HCOOH exclusively and preventing unwanted H2 production at the same time.

PMID:
26996154
DOI:
10.1039/c6cp00542j

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