Hydroxylated TiO2-induced high-density Ni clusters for breaking the activity-selectivity trade-off of CO2 hydrogenation

Abstract

The reverse water gas shift reaction can be considered as a promising route to mitigate global warming by converting CO₂ into syngas in a large scale, while it is still challenging for non-Cu-based catalysts to break the trade-off between activity and selectivity. Here, the relatively high loading of Ni species is highly dispersed on hydroxylated TiO₂ through the strong Ni and −OH interactions, thereby inducing the formation of rich and stable Ni clusters (~1 nm) on anatase TiO₂ during the reverse water gas shift reaction. This Ni cluster/TiO₂ catalyst shows a simultaneous high CO₂ conversion and high CO selectivity. Comprehensive characterizations and theoretical calculations demonstrate Ni cluster/TiO₂ interfacial sites with strong CO₂ activation capacity and weak CO adsorption are responsible for its unique catalytic performances. This work disentangles the activity-selectivity trade-off of the reverse water gas shift reaction, and emphasizes the importance of metal−OH interactions on surface.

Here, the authors report a Ni(cluster)/TiO₂ catalyst with strong interactions between Ni and −OH strong to promote CO₂ activation with CO adsorption to avoid the activity-selectivity trade-off of the reverse water gas shift reaction.