Molecular engineering to introduce carbonyl between nickel salophen active sites to enhance electrochemical CO2 reduction to methanol

The electrochemical reduction of CO2 to methanol is a potentially cost-effective strategy to reduce the concentration of this greenhouse gas while at the same time producing a value-added chemical. Herein, we detail a highly efficient 2D nickel organic framework containing a large density of highly...

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Detalles Bibliográficos
Autores: Liang, Zhifu, Wang, Jianghao, Tang, Pengyi, Tang, Weiqiang, Liu, Lijia, Shakouri, Mohsen, Wang, Xiang, Llorca Piqué, Jordi|||0000-0002-7447-9582, Zhao, Shuangliang, Heggen, Marc, Dunin-Borkowski, Rafal E., Cabot, Andreu, Bin Wu, Hao, Arbiol, Jordi
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/377536
Acceso en línea:https://hdl.handle.net/2117/377536
https://dx.doi.org/10.1016/j.apcatb.2022.121451
Access Level:acceso abierto
Palabra clave:Electrocatalysis
Two dimensional p-d organic frameworks
Atomically dispersed nickel
Carbonyl group
Electrocatalytic CO2 reduction
Methanol
Electrocatàlisi
Àrees temàtiques de la UPC::Enginyeria química
Descripción
Sumario:The electrochemical reduction of CO2 to methanol is a potentially cost-effective strategy to reduce the concentration of this greenhouse gas while at the same time producing a value-added chemical. Herein, we detail a highly efficient 2D nickel organic framework containing a large density of highly dispersed salophen NiN2O2 active sites toward electrochemical CO2RR to methanol. By tuning the ligand environment of the salophen NiN2O2, the electrocatalytic activity of the material toward CO2 reduction can be significantly improved. We prove that by introducing a carbonyl group at the ligand environment of the Ni active sites, the electrochemical CO2 reduction activity is highly promoted and its product selectivity reaches a Faradaic efficiency of 27% toward the production of methanol at - 0.9 V vs RHE. The salophen-based p-d conjugated metal-organic framework presented here thus provides the best performance toward CO2 reduction to methanol among the previously developed nickel-based electrocatalysts.