Elastic Ag-anchored N-doped graphene/carbon foam for the selective electrochemical reduction of carbon dioxide to ethanol. Issue 12 (2nd March 2018)
- Record Type:
- Journal Article
- Title:
- Elastic Ag-anchored N-doped graphene/carbon foam for the selective electrochemical reduction of carbon dioxide to ethanol. Issue 12 (2nd March 2018)
- Main Title:
- Elastic Ag-anchored N-doped graphene/carbon foam for the selective electrochemical reduction of carbon dioxide to ethanol
- Authors:
- Lv, Kuilin
Fan, Yanchen
Zhu, Ying
Yuan, Yi
Wang, Jinrong
Zhu, Ying
Zhang, Qianfan - Abstract:
- Abstract : 3D macroporous hierarchical Ag-G-NCF can efficiently convert CO2 to ethanol with a low overpotential, high faradaic efficiency and high selectivity. Abstract : Electrochemical reduction of CO2 is considered to be an efficient strategy for converting CO2 emissions into valued-added carbon compounds. However, it often suffers from high overpotential, low product faradaic efficiency and poor selectivity for the desired products. Herein, a cost-effective method was designed to anchor Ag nanoparticles onto 3D graphene-wrapped nitrogen-doped carbon foam (Ag-G-NCF) by direct carbonization of melamine foam loaded with graphene oxide and silver salt. Directly acting as a high-efficiency electrode for CO2 electrochemical reduction, the Ag-G-NCF can efficiently and preferentially convert CO2 to ethanol with faradaic efficiencies (FEs) of 82.1–85.2% at −0.6 to −0.7 V ( vs. RHE), overcoming the usual limitation of low FE and selectivity for C2 products. Density functional theory calculations confirmed that the pyridinic N species of the Ag-G-NCF catalyst exhibited a higher bonding ability toward CO* intermediates than other N species, and that then the Ag particles gradually converted the CO* to the OC–COH intermediate of ethanol. Its excellent performance in CO2 electroreduction can be attributed to a combination of the synergistic catalysis occurring between the pyridinic N present at high content and the Ag nanoparticles, the hierarchical macroporous structure, and the goodAbstract : 3D macroporous hierarchical Ag-G-NCF can efficiently convert CO2 to ethanol with a low overpotential, high faradaic efficiency and high selectivity. Abstract : Electrochemical reduction of CO2 is considered to be an efficient strategy for converting CO2 emissions into valued-added carbon compounds. However, it often suffers from high overpotential, low product faradaic efficiency and poor selectivity for the desired products. Herein, a cost-effective method was designed to anchor Ag nanoparticles onto 3D graphene-wrapped nitrogen-doped carbon foam (Ag-G-NCF) by direct carbonization of melamine foam loaded with graphene oxide and silver salt. Directly acting as a high-efficiency electrode for CO2 electrochemical reduction, the Ag-G-NCF can efficiently and preferentially convert CO2 to ethanol with faradaic efficiencies (FEs) of 82.1–85.2% at −0.6 to −0.7 V ( vs. RHE), overcoming the usual limitation of low FE and selectivity for C2 products. Density functional theory calculations confirmed that the pyridinic N species of the Ag-G-NCF catalyst exhibited a higher bonding ability toward CO* intermediates than other N species, and that then the Ag particles gradually converted the CO* to the OC–COH intermediate of ethanol. Its excellent performance in CO2 electroreduction can be attributed to a combination of the synergistic catalysis occurring between the pyridinic N present at high content and the Ag nanoparticles, the hierarchical macroporous structure, and the good conductivity. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 6:Issue 12(2018)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 6:Issue 12(2018)
- Issue Display:
- Volume 6, Issue 12 (2018)
- Year:
- 2018
- Volume:
- 6
- Issue:
- 12
- Issue Sort Value:
- 2018-0006-0012-0000
- Page Start:
- 5025
- Page End:
- 5031
- Publication Date:
- 2018-03-02
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ta10802h ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
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