Oxidative dehydrogenation of C <sub>2</sub> H <sub>6</sub> and CO <sub>2</sub> mediated by Rh <sub> <i>x</i> </sub> Nb <sub> <i>y</i> </sub> <sup>−</sup> ( <i>x</i> + <i>y</i> = 5) clusters
Oxidative dehydrogenation (ODHE) of C<sub>2</sub>H<sub>6</sub> and CO<sub>2</sub> to generate C<sub>2</sub>H<sub>4</sub> and CO is industrially important but remains a long-standing challenge due to the complexity of this co-conversion and the thermodynamically stable and kinetically inert nature of both reactants. Herein, we theoretically demonstrated that the Rh<sub><i>x</i></sub>Nb<sub><i>y</i></sub><sup>-</sup> (<i>x</i> + <i>y</i> = 5) bimetallic clusters can drive the ODHE of C<sub>2</sub>H<sub>6</sub> and CO<sub>2</sub> to produce C<sub>2</sub>H<sub>4</sub>, CO, and H<sub>2</sub>O. The results indicated that the desorption of C<sub>2</sub>H<sub>4</sub> and CO takes place under mild conditions, and the increased number of Rh atoms in Rh<sub><i>x</i></sub>Nb<sub><i>y</i></sub><sup>-</sup> leads to progressively more difficult C<sub>2</sub>H<sub>4</sub> desorption. In contrast, the formation and evaporation of H<sub>2</sub>O represent the kinetically and thermodynamically demanding pathway to govern the overall efficiency of ODHE. This finding provides an integrated picture to understand the fundamental mechanisms of the ODHE of C<sub>2</sub>H<sub>6</sub> and CO<sub>2</sub>. The selective release of C<sub>2</sub>H<sub>4</sub> and the rate-determining behaviour of H<sub>2</sub>O generation were rationalized.
Authors
- Hong Zhu (ORCID: https://orcid.org/0000-0002-2575-4031)
- Xiao‐Na Li (ORCID: https://orcid.org/0000-0002-0316-5762)
- Xue‐Jie Sun
Institutions
- Beijing Institute of Technology (CN)
Publication Details
- Journal
- Dalton Transactions
- Published
- 2025-12-02
- DOI
- https://doi.org/10.1039/d5dt02594j
- Primary Topic
- Catalysis and Oxidation Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00