Boosting the performance of Ni/AlO for the reverse water gas shift reaction through formation of CuNi nanoalloys

Ni supported on alumina is extensively employed as a catalyst for the reverse water gas shift reaction. However, the formation of inactive Ni aluminates and the high selectivity to methane affects the performance of these catalysts, especially at low reaction temperatures. In this study, Cu is emplo...

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Bibliographic Details
Published inCatalysis science & technology Vol. 12; no. 2; pp. 474 - 487
Main Authors Gioria, Esteban, Ingale, Piyush, Pohl, Felix, Naumann d'Alnoncourt, Raoul, Thomas, Arne, Rosowski, Frank
Format Journal Article
Published 26.01.2022
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Summary:Ni supported on alumina is extensively employed as a catalyst for the reverse water gas shift reaction. However, the formation of inactive Ni aluminates and the high selectivity to methane affects the performance of these catalysts, especially at low reaction temperatures. In this study, Cu is employed as an effective enhancer of the catalytic performance, promoting the reducibility of Ni, and suppressing methane production through the formation of stable CuNi nanoalloys. The synergy between both metals suppresses consecutive hydrogenation, reaching conversions close to equilibrium and 100% selectivity to carbon monoxide. At 500 °C, the CO yield of the Cu 25 Ni 75 /Al 2 O 3 catalyst was twice that of Ni/Al 2 O 3 , with only half the hydrogen consumption. The formation of CuNi nanoalloys was confirmed by HAADF STEM-EDS, without segregation in monometallic phases even after 30 h time on stream. Similarly, Cu 50 Ni 50 /Al 2 O 3 remained alloyed after the reaction. However, the catalytic activity decreased due to sintering, in agreement with a higher Cu content. This effect was significantly more pronounced for Cu 75 Ni 25 /Al 2 O 3 and Cu/Al 2 O 3 , with formation of large particles and consequent loss of active surface area. Adding Cu to Ni/Al 2 O 3 is an excellent strategy to suppress methane formation and enhance carbon monoxide yield through formation of alloyed nanoparticles.
Bibliography:10.1039/d1cy01585k
Electronic supplementary information (ESI) available. See DOI
ISSN:2044-4753
2044-4761
DOI:10.1039/d1cy01585k