New Trends in Electrocatalysis for CO2 Conversion

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Electrocatalysis".

Deadline for manuscript submissions: closed (10 July 2023) | Viewed by 4367

Special Issue Editors


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Guest Editor
Department of Chemical Science and Technologies, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy
Interests: development of metal oxides for applications in reversible solid oxide cells (RSOCs)

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Guest Editor
Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Via Anguillarese 301, 00123 Rome, Italy
Interests: gas–solid reaction; CO2 capture and valorization; multiphase modeling; sustainable technologies
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Special Issue Information

Dear Colleagues,

The ever-increasing emissions of carbon dioxide resulting from an unbalanced carbon cycle are primarily responsible for global warming. The imbalance between emitted and recycled CO2 results from human activity. Specifically, the combustion of fossil fuels such as coal, oil, and natural gas contributes to increasing the level of carbon dioxide in the atmosphere, reaching 413 ppm by the end of 2021, around 50% higher than the pre-industrial revolution level. Since the complete replacement of fossil fuels (and the energy transition towards renewable energy sources with zero or negative CO2 footprint) still seems far from taking place, it is of paramount importance to tackle carbon dioxide accumulation by developing new CO2 utilization technologies.

The possibility to convert CO2 into valuable and easy-to-store chemicals, ranging from carbon monoxide to methanol, ethanol, ethylene, and formic acid, has opened several ways to accomplish CO2 reduction reaction (CO2RR) using photochemical, biochemical, thermochemical, and electrochemical routes. Electrochemical CO2RR offers several advantages, such as the possibility of operation at ambient temperature and pressure, tunable reaction rates, scalability through electrolyzer modular connection, and electrolyte recyclability. Moreover, excess energy coming from renewable energy sources can be exploited to drive the carbon dioxide reduction process.

Nevertheless, electrochemical CO2 conversion is still far from reaching a mature commercial level, mainly because of challenging product selectivity, competing reactions, and sluggish CO2 activation. Thus, developing efficient, highly selective, and cost-effective electrocatalysts is a crucial aspect.

This Special Issue will focus on the newest trends in CO2RR electrocatalyst development and application, covering both low-temperature and high-temperature systems. The design of heterogeneous catalysts, their ex situ or in situ characterization, and final testing will be of interest. The focus on insights of reaction mechanisms and different pathways will be relevant both from fundamental and applied perspectives. The final purpose is providing a collection of valuable manuscripts that will contribute to shed light on CO2 electrocatalytic conversion.

Dr. Leonardo Duranti
Dr. Igor Luisetto
Guest Editors

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Keywords

  • electrochemical CO2 reduction
  • electrocatalysis
  • molecular catalyst
  • electrochemistry
  • solid oxide electrolyzer cell
  • CO2RR mechanisms
  • electrolyte
  • electrodes
  • material design
  • cell configuration

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Published Papers (2 papers)

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Research

18 pages, 10185 KiB  
Article
Structured Catalyst for Indirect Internal Reforming (IIR) of Biogas in Solid Oxide Fuel Cell (SOFC)
by Anna Prioriello, Leonardo Duranti, Igor Luisetto, Frederick Sanna, Claudio Larosa, Maria Luisa Grilli and Elisabetta Di Bartolomeo
Catalysts 2023, 13(7), 1129; https://doi.org/10.3390/catal13071129 - 20 Jul 2023
Cited by 4 | Viewed by 2061
Abstract
The aim of this work is the development of a structured catalyst for the dry reforming of biogas to be used as a pre–reformer in the indirect internal reforming configuration (IIR) of solid oxide fuel cells (SOFCs). The structured catalyst is based on [...] Read more.
The aim of this work is the development of a structured catalyst for the dry reforming of biogas to be used as a pre–reformer in the indirect internal reforming configuration (IIR) of solid oxide fuel cells (SOFCs). The structured catalyst is based on NiCrAl foams coated with ruthenium (nominal loading 3.0 wt%) supported on a CaZr0.85Sm0.15O3−δ (CZS) perovskite oxide. The powder is produced by solution combustion synthesis and deposited on metallic foams by the wash–coating method. Catalytic tests for the dry reforming of methane (DRM) reaction are carried out at 850 °C, 700 °C and 550 °C for an overall 50 h with CH4/CO2 = 1 and p = 1.3 bar at different gas hourly space velocities (GHSVs). The final goal is a proof–of–concept: a laboratory validation of an IIR–SOFC fed by biogas. The carbon amount on spent structured catalysts is evaluated by thermogravimetric analysis and microstructural/compositional investigation. Full article
(This article belongs to the Special Issue New Trends in Electrocatalysis for CO2 Conversion)
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10 pages, 2830 KiB  
Article
Enhanced Electrolysis of CO2 with Metal–Oxide Interfaces in Perovskite Cathode in Solid Oxide Electrolysis Cell
by Guoliang Ma, Yihong Xu and Kui Xie
Catalysts 2022, 12(12), 1607; https://doi.org/10.3390/catal12121607 - 8 Dec 2022
Cited by 3 | Viewed by 1730
Abstract
The application of solid oxide electrolysis cell in CO2 electroreduction is a hot research topic at present, but the development of low−cost catalysts with high catalytic activity has always been a challenge for this work. Herein, we use NiCu alloy nanoparticles to [...] Read more.
The application of solid oxide electrolysis cell in CO2 electroreduction is a hot research topic at present, but the development of low−cost catalysts with high catalytic activity has always been a challenge for this work. Herein, we use NiCu alloy nanoparticles to modify the perovskite LSCM electrode to build a metal–oxide active interface to obtain high catalytic performance. At 850 °C, 4.66 mL min−1 cm−2 CO productivity and 97.7% Faraday current efficiency were obtained. In addition, the current remained stable during the 100 h long−term test, indicating that the active interface has the dual effect of improving catalytic performance and maintaining cell durability. Full article
(This article belongs to the Special Issue New Trends in Electrocatalysis for CO2 Conversion)
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