Loading…

Energy efficient electrochemical reduction of CO 2 to CO using a three-dimensional porphyrin/graphene hydrogel

Although electrochemical CO 2 reduction is one of the most promising ways to convert atmospheric CO 2 into value-added chemicals, there are still numerous limitations to overcome to achieve highly efficient CO 2 conversion performance. Herein, we report for the first time the development and use of...

Full description

Saved in:
Bibliographic Details
Published in:Energy & environmental science 2019-02, Vol.12 (2), p.747-755
Main Authors: Choi, Jaecheol, Kim, Jeonghun, Wagner, Pawel, Gambhir, Sanjeev, Jalili, Rouhollah, Byun, Seoungwoo, Sayyar, Sepidar, Lee, Yong Min, MacFarlane, Douglas R., Wallace, Gordon G., Officer, David L.
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Although electrochemical CO 2 reduction is one of the most promising ways to convert atmospheric CO 2 into value-added chemicals, there are still numerous limitations to overcome to achieve highly efficient CO 2 conversion performance. Herein, we report for the first time the development and use of a three-dimensional iron porphyrin-based graphene hydrogel (FePGH) as an electrocatalyst for extremely efficient robust CO 2 reduction to CO. Electrocatalytic CO 2 conversion was performed in aqueous medium with FePGH, which has a highly porous and conductive 3D graphene structure, resulting in high catalytic activity for CO production with ∼96.2% faradaic efficiency at a very low overpotential of 280 mV. Furthermore, FePGH showed considerable catalytic durability maintaining a consistent CO yield (96.4% FE) over 20 h electrolysis at the same overpotential, corresponding to the highest cathodic energy efficiency yet observed of 79.7% compared to other state-of-the-art immobilised metal complex electrocatalysts. This approach to fabricating a 3D graphene-based hydrogel electrocatalyst should provide an exciting new avenue for the development of other kinds of molecular electrocatalysts.
ISSN:1754-5692
1754-5706
DOI:10.1039/C8EE03403F