Issue 11, 2019

Hydroxyl-mediated ethanol selectivity of CO2 hydrogenation

Abstract

Oxide-supported Rh nanoparticles have been widely used for CO2 hydrogenation, especially for ethanol synthesis. However, this reaction operates under high pressure, up to 8 MPa, and suffers from low CO2 conversion and alcohol selectivity. This paper describes the crucial role of hydroxyl groups bound on Rh-based catalysts supported on TiO2 nanorods (NRs). The RhFeLi/TiO2 NR catalyst shows superior reactivity (≈15% conversion) and ethanol selectivity (32%) for CO2 hydrogenation. The promoting effect can be attributed to the synergism of high Rh dispersion and high-density hydroxyl groups on TiO2 NRs. Hydroxyls are proven to stabilize formate species and protonate methanol, which is easily dissociated into *CHx, and then CO obtained from the reverse water–gas shift reaction (RWGS) is inserted into *CHx to form CH3CO*, followed by CH3CO* hydrogenation to ethanol.

Graphical abstract: Hydroxyl-mediated ethanol selectivity of CO2 hydrogenation

Supplementary files

Article information

Article type
Edge Article
Submitted
16 des. 2018
Accepted
11 feb. 2019
First published
11 feb. 2019
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2019,10, 3161-3167

Hydroxyl-mediated ethanol selectivity of CO2 hydrogenation

C. Yang, R. Mu, G. Wang, J. Song, H. Tian, Z. Zhao and J. Gong, Chem. Sci., 2019, 10, 3161 DOI: 10.1039/C8SC05608K

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