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Carbon nitride boosts the CO2 methanation activity of Ni/CeO2

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ZHAO Yingrui HONGMANOROM Plaifa YANG Feilong CASALE Sandra SASSOYE Capucine STÝSKALÍK Aleš DEBECKER Damien P.

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://www.sciencedirect.com/science/article/pii/S2213343725038497?via%3Dihub#ack0005
Doi https://doi.org/10.1016/j.jece.2025.119153
Klíčová slova C3N4; Ceria; Nickel; Methane; CO2 hydrogenation
Popis Selective CO2 methanation using green H-2 offers a promising approach for tackling both energy and environmental challenges. Herein, a Ni/CeO2 catalyst was synthesized using a one-pot method in the presence of sacrificial C3N4 and evaluated for COQ methanation. The catalyst exhibited a high CO2 conversion of 82.6 % and a CH4 production rate of up to 178 mmol g(cat)(-1) h(-1), with high CH4 selectivity (99.4 %) at a remarkably low temperature of 250 degrees C. Surface characterization techniques, including Raman spectroscopy, XPS, P-31-MAS NMR of adsorbed trimethylphosphine, and CO2-TPD, demonstrate that the addition of C3N4 significantly enhanced the concentration of surface oxygen vacancies and medium-strength basic sites. In situ DRIFTS analysis indicated that CO2 methanation over Ni/CeO2 proceeded via the RWGS+CO hydrogenation and formate pathways, with the former being predominant at low temperatures. The exceptional low-temperature methanation performance of this new catalyst is attributed to the increased density of oxygen vacancies and medium-strength basic sites.

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