Electrode surface modifications towards the Electrosynthesis of Ethylene from CO2
Electrode surface modifications towards the Electrosynthesis of Ethylene from CO2
The substitution of fossil based production routes with new and innovative synthesis strategies for bulk chemicals as well as fuels or fuel additives will become a strategic goal within the next decade. One promising avenue is the use of CO2 as a carbon source in the synthesis of useful materials such as methanol or ethylene.1, 2 Such reactions have been successfully demonstrated at copper electrodes, which seem uniquely qualified to give a range of possible end products for CO2 reduction.3, 4 Unfortunately, this success is also the major limitation to this method, as the wide number of products results in selectivity issues when trying to produce one specific target molecule. In this work, we focus on the development of a CO2-based electrosynthesis of ethylene at copper working electrodes. Building on existing studies that probed the impact of crystal face, electrolyte and pH on product selectivity,5-7 we use a series of targeted pre-treatment regimes in order to favour ethylene production. These range from simple alterations in the potential waveform, through to surface enhancements through roughening, nanostructuring and electrodeposition. Through these, we move towards defining an easily accessible surface structure that gives sufficient selectivity towards ethylene to provide a useful, and eventually scalable route to ethylene synthesis from CO2.
Perry, Samuel
8e204d86-4a9c-4a5d-9932-cf470174648e
Ponce De Leon Albarran, Carlos
508a312e-75ff-4bcb-9151-dacc424d755c
Wang, Ling
c50767b1-7474-4094-9b06-4fe64e9fe362
16 September 2018
Perry, Samuel
8e204d86-4a9c-4a5d-9932-cf470174648e
Ponce De Leon Albarran, Carlos
508a312e-75ff-4bcb-9151-dacc424d755c
Wang, Ling
c50767b1-7474-4094-9b06-4fe64e9fe362
Perry, Samuel, Ponce De Leon Albarran, Carlos and Wang, Ling
(2018)
Electrode surface modifications towards the Electrosynthesis of Ethylene from CO2.
Electrochem 2018, Lancaster University, Lancaster, United Kingdom.
16 - 18 Sep 2018.
Record type:
Conference or Workshop Item
(Paper)
Abstract
The substitution of fossil based production routes with new and innovative synthesis strategies for bulk chemicals as well as fuels or fuel additives will become a strategic goal within the next decade. One promising avenue is the use of CO2 as a carbon source in the synthesis of useful materials such as methanol or ethylene.1, 2 Such reactions have been successfully demonstrated at copper electrodes, which seem uniquely qualified to give a range of possible end products for CO2 reduction.3, 4 Unfortunately, this success is also the major limitation to this method, as the wide number of products results in selectivity issues when trying to produce one specific target molecule. In this work, we focus on the development of a CO2-based electrosynthesis of ethylene at copper working electrodes. Building on existing studies that probed the impact of crystal face, electrolyte and pH on product selectivity,5-7 we use a series of targeted pre-treatment regimes in order to favour ethylene production. These range from simple alterations in the potential waveform, through to surface enhancements through roughening, nanostructuring and electrodeposition. Through these, we move towards defining an easily accessible surface structure that gives sufficient selectivity towards ethylene to provide a useful, and eventually scalable route to ethylene synthesis from CO2.
This record has no associated files available for download.
More information
Published date: 16 September 2018
Additional Information:
CO2 Reduction and Artificial Fuel
Venue - Dates:
Electrochem 2018, Lancaster University, Lancaster, United Kingdom, 2018-09-16 - 2018-09-18
Identifiers
Local EPrints ID: 472712
URI: http://eprints.soton.ac.uk/id/eprint/472712
PURE UUID: 5a67df4d-1cfd-4e64-a931-1e0c2c2307ba
Catalogue record
Date deposited: 15 Dec 2022 17:38
Last modified: 11 Jun 2024 01:55
Export record
Contributors
Author:
Samuel Perry
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics