Balancing performance and sustainability in integrated CO₂ capture and methanation via NiCeO₂-anionic clay hybrid materials
Year: 2026
Type: article
Abstract: Integrated CO₂ capture and methanation (ICCM) provides a direct route for converting captured CO₂ into synthetic methane, but its large-scale implementation is limited by material stability and sustainability. Here, we report NiCeO₂/ionic clay hybrid materials, where the ionic clay is a Mg–Al carbonate layered double hydroxide (LDH) acting as an adsorbent matrix for NiCeO₂ catalytic nanoparticles. The hybrids exhibit enhanced CO₂ uptake, efficient low-temperature operation (300 °C) with 100% CH₄ selectivity, and excellent cyclic stability under ICCM conditions. Although the NiCeO₂/LDH hybrids show lower methane productivity per unit mass of total material than NiCeO₂ alone, they significantly improve catalyst utilization, producing up to four times more CH₄ per unit mass of NiCeO₂. Operando XANES reveals a reversible Ni⁰/Ni²⁺ redox transition under alternating CO₂/H₂ atmospheres, demonstrating that the active Ni phase dynamically adjusts its oxidation state during CO₂ adsorption–hydrogenation cycles. Life cycle assessment demonstrates a markedly reduced environmental footprint for the hybrid materials compared with NiCeO₂ for the same methane output, highlighting NiCeO₂/LDH hybrids as sustainable and scalable platforms for integrated CO₂ capture and conversion.
Source: Chemical Engineering Journal
Institutions: Lyon 1 Université, Centre National de la Recherche Scientifique, Institut de Recherches sur la Catalyse et l'Environnement de Lyon, Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé, Université de Strasbourg, Université de Haute-Alsace, Institut de Sciences des Matériaux de Mulhouse, European Synchrotron Radiation Facility, Technical University of Crete
Language: English
Subfield: Catalysis
Field: Chemical Engineering
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,830
Awards: G3508424599, G5486846836
OpenAlex ID: W7167634959
