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Production of formate by CO2 electrochemical reduction and its application in energy storage

Production of formate by CO2 electrochemical reduction and its application in energy storage
Production of formate by CO2 electrochemical reduction and its application in energy storage

Production of liquid fuels by electrochemical CO2 reduction (eCO2R) is an attractive option for energy storage in the form of renewable energy. This study focuses on efficient formate production using an eCO2R system and its application in generating power using a direct formate fuel cell (DFFC). A carbon black supported SnO2 catalyst was used for the eCO2R in a gas diffusion reactor using a 1.0 M KOH electrolyte. An average faradaic efficiency of 80% for formate production was achieved over a wide electrode potential range (-0.63 to -1.43 V vs. RHE). Since the overall current density varied linearly with the overpotential, the rate of formate production could be easily controlled by varying the applied potential. At a current density of 251 mA cm-2 (-1.43 V), a high formate production rate was achieved at 3 mg min-1 cmWE-2 resulting in 0.5 M formate being produced within 1 hour. This formate solution was directly used as the fuel for a DFFC, without pre-treatment. The fuel cell consisted of a Pd-CeO2/C anode and FeCo/C cathode and produced a peak power density of 92 mW cm-2. A closed loop of "electricity-formate-electricity" has been realized in this study, signifying the promising future of sustainable CO2 conversion to liquid fuels for CO2 fixation as well as for energy storage.

277-284
Xiang, Hang
c2751c29-e8d9-485f-9899-b84287361dd8
Miller, Hamish Andrew
8d2693c0-dfd3-4266-ae61-a1d8ca9df370
Bellini, Marco
ecedc852-a808-41b4-8f27-0fed09cd8955
Christensen, Henriette
a7a18afa-360f-4741-99c9-ffa6e2e92446
Scott, Keith
38909157-296d-4fe7-a245-1b98e1fee913
Rasul, Shahid
482cda2a-0a01-4f15-846a-c4aa2f73b824
Yu, Eileen H.
28e47863-4b50-4821-b80b-71fb5a2edef2
Xiang, Hang
c2751c29-e8d9-485f-9899-b84287361dd8
Miller, Hamish Andrew
8d2693c0-dfd3-4266-ae61-a1d8ca9df370
Bellini, Marco
ecedc852-a808-41b4-8f27-0fed09cd8955
Christensen, Henriette
a7a18afa-360f-4741-99c9-ffa6e2e92446
Scott, Keith
38909157-296d-4fe7-a245-1b98e1fee913
Rasul, Shahid
482cda2a-0a01-4f15-846a-c4aa2f73b824
Yu, Eileen H.
28e47863-4b50-4821-b80b-71fb5a2edef2

Xiang, Hang, Miller, Hamish Andrew, Bellini, Marco, Christensen, Henriette, Scott, Keith, Rasul, Shahid and Yu, Eileen H. (2019) Production of formate by CO2 electrochemical reduction and its application in energy storage. Sustainable Energy and Fuels, 4 (1), 277-284. (doi:10.1039/c9se00625g).

Record type: Article

Abstract

Production of liquid fuels by electrochemical CO2 reduction (eCO2R) is an attractive option for energy storage in the form of renewable energy. This study focuses on efficient formate production using an eCO2R system and its application in generating power using a direct formate fuel cell (DFFC). A carbon black supported SnO2 catalyst was used for the eCO2R in a gas diffusion reactor using a 1.0 M KOH electrolyte. An average faradaic efficiency of 80% for formate production was achieved over a wide electrode potential range (-0.63 to -1.43 V vs. RHE). Since the overall current density varied linearly with the overpotential, the rate of formate production could be easily controlled by varying the applied potential. At a current density of 251 mA cm-2 (-1.43 V), a high formate production rate was achieved at 3 mg min-1 cmWE-2 resulting in 0.5 M formate being produced within 1 hour. This formate solution was directly used as the fuel for a DFFC, without pre-treatment. The fuel cell consisted of a Pd-CeO2/C anode and FeCo/C cathode and produced a peak power density of 92 mW cm-2. A closed loop of "electricity-formate-electricity" has been realized in this study, signifying the promising future of sustainable CO2 conversion to liquid fuels for CO2 fixation as well as for energy storage.

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More information

Accepted/In Press date: 19 October 2019
Published date: 9 December 2019
Additional Information: Publisher Copyright: © 2019 The Royal Society of Chemistry.

Identifiers

Local EPrints ID: 498644
URI: http://eprints.soton.ac.uk/id/eprint/498644
PURE UUID: 3d88b732-5d73-4d66-8b55-556b8b4747e2
ORCID for Eileen H. Yu: ORCID iD orcid.org/0000-0002-6872-975X

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Date deposited: 24 Feb 2025 18:10
Last modified: 25 Feb 2025 03:14

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Contributors

Author: Hang Xiang
Author: Hamish Andrew Miller
Author: Marco Bellini
Author: Henriette Christensen
Author: Keith Scott
Author: Shahid Rasul
Author: Eileen H. Yu ORCID iD

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