Publication: Electrochemical CO2 reduction to gaseous methane and carbon monoxide using plasma-synthesized copper nanowires
dc.contributor.coauthor | Butt, Faaz Ahmed | |
dc.contributor.coauthor | Alshahrani, Thamraa | |
dc.contributor.coauthor | Awan, Zahoor Ul Hussain | |
dc.contributor.coauthor | Christy, Maria | |
dc.contributor.coauthor | Khan, Firoz | |
dc.contributor.coauthor | Alanazi, Abdulaziz M. | |
dc.contributor.department | Department of Chemistry | |
dc.contributor.kuauthor | Ünal, Uğur | |
dc.contributor.other | Department of Chemistry | |
dc.contributor.schoolcollegeinstitute | College of Sciences | |
dc.date.accessioned | 2024-12-29T09:41:05Z | |
dc.date.issued | 2023 | |
dc.description.abstract | There is a growing interest among environmental researchers to synthesize a sustainable catalyst for CO2 conversion process. Copper and modified copper offer a wide window for such catalysts. In this study, we report the use of plasma-treated copper/copper oxide nanowires for electrochemical CO2 reduction for the first time. Plasma-treated Cu nanowires (CuO-P NWs) were comparatively evaluated with bulk copper surface in CO2 saturated test solutions, namely, KHCO3, KCl, and NaCl, with 0.1 and 1 M concentrations. CuO-P NWs demonstrate 50% increase in selectivity towards CO2 reduced gaseous products (CO and CH4) at a higher applied potential of - 1.1 V vs reversible hydrogen electrode. This increased selectivity is associated with decreased binding energy of the intermediate species on plasma-treated nanowires compared to bulk surface. Both CO and CH4 were the main products detected in the gaseous state, and CO is suggested as the main intermediate species. The effects of different cations and anions and their concentrations in the solutions were also analyzed. It was observed that dilute solutions in 0.1 M are optimal for electrochemical CO2 reduction (ECO2R) and that hydration energy of cations plays a significant role in ECO2R selectivity, while hydrogen evolution reaction was the competing reaction. | |
dc.description.indexedby | WoS | |
dc.description.indexedby | Scopus | |
dc.description.publisherscope | International | |
dc.description.sponsors | This research was funded by Princess Nourah bint Abdulrahman University Researchers Supporting Project number (PNURSP2023R1), Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia. The authors would also like to acknowledge the support and funding provided by KOC University, KOC University Surface Science and Technology Center (KUYTAM), and NED University of Engineering and Technology and Higher Education Commission, Pakistan. | |
dc.identifier.doi | 10.1007/s10008-023-05600-z | |
dc.identifier.eissn | 1433-0768 | |
dc.identifier.issn | 1432-8488 | |
dc.identifier.quartile | Q3 | |
dc.identifier.scopus | 2-s2.0-85166207752 | |
dc.identifier.uri | https://doi.org/10.1007/s10008-023-05600-z | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/23522 | |
dc.identifier.wos | 1040840600001 | |
dc.keywords | CO2 electroreduction | |
dc.keywords | Hydrocarbons | |
dc.keywords | Carbon monoxide | |
dc.keywords | Methane | |
dc.keywords | Plasma treatment | |
dc.keywords | Copper nanowires | |
dc.keywords | Carbon cycle | |
dc.language | en | |
dc.publisher | Springer | |
dc.relation.grantno | Princess Nourah bint Abdulrahman University [PNURSP2023R1] | |
dc.relation.grantno | Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia | |
dc.relation.grantno | KOC University, KOC University Surface Science and Technology Center (KUYTAM) | |
dc.relation.grantno | NED University of Engineering and Technology and Higher Education Commission, Pakistan | |
dc.source | Journal of Solid State Electrochemistry | |
dc.subject | Electrochemistry | |
dc.title | Electrochemical CO2 reduction to gaseous methane and carbon monoxide using plasma-synthesized copper nanowires | |
dc.type | Journal article | |
dc.type.other | Early access | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Ünal, Uğur | |
relation.isOrgUnitOfPublication | 035d8150-86c9-4107-af16-a6f0a4d538eb | |
relation.isOrgUnitOfPublication.latestForDiscovery | 035d8150-86c9-4107-af16-a6f0a4d538eb |