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Structure-Sensitive CO2 Electroreduction to Hydrocarbons on Ultrathin 5-fold Twinned Copper Nanowires.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Li, Yifan Ross, Michael B. Kim, Dohyung Sun, Yuchun Yang, Peidong |
| Copyright Year | 2017 |
| Abstract | Copper is uniquely active for the electrocatalytic reduction of carbon dioxide (CO2) to products beyond carbon monoxide, such as methane (CH4) and ethylene (C2H4). Therefore, understanding selectivity trends for CO2 electrocatalysis on copper surfaces is critical for developing more efficient catalysts for CO2 conversion to higher order products. Herein, we investigate the electrocatalytic activity of ultrathin (diameter ∼20 nm) 5-fold twinned copper nanowires (Cu NWs) for CO2 reduction. These Cu NW catalysts were found to exhibit high CH4 selectivity over other carbon products, reaching 55% Faradaic efficiency (FE) at -1.25 V versus reversible hydrogen electrode while other products were produced with less than 5% FE. This selectivity was found to be sensitive to morphological changes in the nanowire catalyst observed over the course of electrolysis. Wrapping the wires with graphene oxide was found to be a successful strategy for preserving both the morphology and reaction selectivity of the Cu NWs. These results suggest that product selectivity on Cu NWs is highly dependent on morphological features and that hydrocarbon selectivity can be manipulated by structural evolution or the prevention thereof. |
| Starting Page | 1312 |
| Ending Page | 1317 |
| Page Count | 6 |
| File Format | PDF HTM / HTML |
| DOI | 10.1021/acs.nanolett.6b05287 |
| PubMed reference number | 28094953 |
| Journal | Medline |
| Volume Number | 17 |
| Issue Number | 2 |
| Alternate Webpage(s) | http://nanowires.berkeley.edu/wp-content/uploads/2017/03/Nano-Letters-2017-Li.pdf |
| Alternate Webpage(s) | https://doi.org/10.1021/acs.nanolett.6b05287 |
| Journal | Nano letters |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |