Lewis‐Basic EDTA as a Highly Active Molecular Electrocatalyst for CO2 Reduction to CH4. (12th September 2021)
- Record Type:
- Journal Article
- Title:
- Lewis‐Basic EDTA as a Highly Active Molecular Electrocatalyst for CO2 Reduction to CH4. (12th September 2021)
- Main Title:
- Lewis‐Basic EDTA as a Highly Active Molecular Electrocatalyst for CO2 Reduction to CH4
- Authors:
- Huang, Minxue
Gong, Shipeng
Wang, Changlai
Yang, Yang
Jiang, Peng
Wang, Pengcheng
Hu, Lin
Chen, Qianwang - Abstract:
- Abstract: The most active catalysts so far successful in hydrogenation reduction of CO2 are mainly heterogeneous Cu‐based catalysts. The complex coordination environments and multiple active sites in heterogeneous catalysts result in low selectivity of target product, while molecular catalysts with well‐defined active sites and tailorable structures allow mechanism‐based performance optimization. Herein, we firstly report a single ethylenediaminetetraacetic acid (EDTA) molecular‐level immobilized on the surface of carbon nanotube as a catalyst for transferring CO2 to CH4 with an excellent performance. This catalyst exhibits a high Faradaic efficiency of 61.6 % toward CH4, a partial current density of −16.5 mA cm −2 at a potential of −1.3 V versus reversible hydrogen electrode. Density functional theory calculations reveal that the Lewis basic COO − groups in EDTA molecule are the active sites for CO2 reduction reaction (CO2 RR). The energy barrier for the generation of CO from *CO intermediate is as high as 0.52 eV, while the further protonation of *CO to *CHO follows an energetic downhill path (−1.57 eV), resulting in the high selectivity of CH4 . This work makes it possible to control the product selectivity for CO2 RR according to the relationship between the energy barrier of *CO intermediate and molecular structures in the future. Abstract : Ethylenediaminetetraacetic acid (EDTA) immobilized on the surface of carbon nanotubes has been identified as active catalyst forAbstract: The most active catalysts so far successful in hydrogenation reduction of CO2 are mainly heterogeneous Cu‐based catalysts. The complex coordination environments and multiple active sites in heterogeneous catalysts result in low selectivity of target product, while molecular catalysts with well‐defined active sites and tailorable structures allow mechanism‐based performance optimization. Herein, we firstly report a single ethylenediaminetetraacetic acid (EDTA) molecular‐level immobilized on the surface of carbon nanotube as a catalyst for transferring CO2 to CH4 with an excellent performance. This catalyst exhibits a high Faradaic efficiency of 61.6 % toward CH4, a partial current density of −16.5 mA cm −2 at a potential of −1.3 V versus reversible hydrogen electrode. Density functional theory calculations reveal that the Lewis basic COO − groups in EDTA molecule are the active sites for CO2 reduction reaction (CO2 RR). The energy barrier for the generation of CO from *CO intermediate is as high as 0.52 eV, while the further protonation of *CO to *CHO follows an energetic downhill path (−1.57 eV), resulting in the high selectivity of CH4 . This work makes it possible to control the product selectivity for CO2 RR according to the relationship between the energy barrier of *CO intermediate and molecular structures in the future. Abstract : Ethylenediaminetetraacetic acid (EDTA) immobilized on the surface of carbon nanotubes has been identified as active catalyst for the electrocatalytic reduction of CO2 to CH4 . A high Faradaic efficiency of 61.6 % for CH4 production is observed. … (more)
- Is Part Of:
- Angewandte Chemie. Volume 133:Number 42(2021)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 133:Number 42(2021)
- Issue Display:
- Volume 133, Issue 42 (2021)
- Year:
- 2021
- Volume:
- 133
- Issue:
- 42
- Issue Sort Value:
- 2021-0133-0042-0000
- Page Start:
- 23184
- Page End:
- 23191
- Publication Date:
- 2021-09-12
- Subjects:
- carbon dioxide -- carbon nanotubes -- electrocatalysis -- EDTA -- molecular catalysts
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.202110594 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21097.xml