Utilizing Carbonaceous Materials Derived from [BMIM][TCM] Ionic Liquid Precursor: Dual Role as Catalysts for Oxygen Reduction Reaction and Adsorbents for Aromatics and CO2

Author:

Tzialla Ourania1,Theodorakopoulos George V.23ORCID,Beltsios Konstantinos G.2,Pilatos George3,Reddy K. Suresh Kumar4,Srinivasakannan Chandrasekar5,Tuci Giulia6,Giambastiani Giuliano67,Karanikolos Georgios N.89,Katsaros Fotios K.3,Kouvelos Evangelos3,Romanos George Em.3

Affiliation:

1. Department of Materials Science and Engineering University of Ioannina 45110 Ioannina Greece

2. School of Chemical Engineering National Technical University of Athens Zografou Campus, 9, Iroon Polytechniou Str. Athens, Zografou 15780 Greece

3. Institute of Nanoscience and Nanotechnology, N.C.S.R. “Demokritos”, Ag. Paraskevi Athens 15310 Greece

4. Renewable and Sustainable Energy Research Center Technology Innovation Institute (TII), P.O. Box 9639, Masdar City Abu Dhabi United Arab Emirates

5. Department of Chemical Engineering Khalifa University Abu Dhabi 127788 United Arab Emirates

6. Institute of Chemistry of OrganoMetallic Compounds, ICCOM-CNR and Consorzio INSTM Via Madonna del Piano, 10 – 50019, Sesto F. no Florence Italy

7. University of Florence, Department of Chemistry U. “Schiff” - DICUS – and INSTM Research Unit, Via della Lastruccia 3-13, 50019 Sesto Fiorentino (FI) Italy

8. Department of Chemical Engineering University of Patras Patras 26504 Greece

9. Institute of Chemical Engineering Sciences Foundation for Research and Technology-Hellas (FORTH/ICE-HT) 26504 Patras Greece

Abstract

AbstractThis work presents the synthesis of N‐doped nanoporous carbon materials using the Ionic Liquid (IL) 1‐butyl‐3‐methylimidazolium tricyanomethanide [BMIM][TCM] as a fluidic carbon precursor, employing two carbonization pathways: templated precursor and pyrolysis/activation. Operando monitoring of mass loss during pyrolytic and activation treatments provides insights into chemical processes, including IL decomposition, polycondensation reactions and pore formation. Comparatively low mass reduction rates were observed at all stages. Heat treatments indicated stable pore size and increasing volume/surface area over time. The resulting N‐doped carbon structures were evaluated as electrocatalysts for the oxygen reduction reaction (ORR) and adsorbents for gases and organic vapors. Materials from the templated precursor pathway exhibited high electrocatalytic performance in ORR, analyzed using Rotating Ring‐Disk electrode (RRDE). Enhanced adsorption of m‐xylene was attributed to wide micropores, while satisfactory CO2 adsorption efficiency was linked to specific morphological features and a relatively high content of N‐sites within the C‐networks. This research contributes valuable insights into the synthesis and applications of N‐doped nanoporous carbon materials, highlighting their potential in electrocatalysis and adsorption processes.

Publisher

Wiley

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