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 wi

SUBMITTER: Wang CX 

PROVIDER: S-EPMC11437244 | biostudies-literature | 2024 Sep

REPOSITORIES: biostudies-literature