Stabilizing Cobalt Catalysts for Aqueous-Phase Reactions by Strong Metal-Support Interaction Article (Faculty180)

cited authors

  • Lee, Jechan; Burt, Samuel P.; Carrero, Carlos A.; Alba-Rubio, Ana C.; Ro, Insoo; O'Neill, Brandon J.; Kim, Hyung Ju; Jackson, David H.K.; Kuech, Thomas F.; Hermans, Ive; Dumesic, James A.; Huber, George W.


  • High-temperature calcination and reduction treatments of cobalt particles (17–20 nm) supported on TiO2 create cobalt particles covered with a TiOy layer. The layer thickness ranges from 2.8 to 4.0 nm. These phenomena, commonly called strong metal-support interaction (SMSI), can be used to improve the catalyst stability and change the catalyst selectivity. For example, non-overcoated cobalt catalysts leached during aqueous-phase hydrogenation (APH) of furfuryl alcohol, losing 44.6% of the cobalt after 35 h time-on-stream. In contrast, TiOy-overcoated cobalt catalysts did not lose any measurable cobalt by leaching and the cobalt particle size remained constant after 105 h time-on-stream. The 1,5-pentanediol selectivity from furfuryl alcohol hydrogenolysis increased with increasing TiOy layer thickness. The stabilized cobalt catalyst also had high yields for APH of xylose to xylitol (99%) and APH of furfural to furfuryl alcohol (95%). These results show that the SMSI effect produces a catalyst with a similar structure as catalysts prepared by atomic layer deposition, thereby opening up a cheaper and more industrially relevant method of stabilizing base-metal catalysts for aqueous-phase biomass conversion reactions. In addition, the SMSI effect can be used to tune catalyst selectivity, thus allowing the more precise atomic scale design of supported metal catalysts.

publication date

  • 2015

published in

start page

  • 19

end page

  • 27


  • 330