Steam‐Assisted Selective CO2 Hydrogenation to Ethanol over Ru−In Catalysts

Author:

Zhou Chengshuang1ORCID,Aitbekova Aisulu2,Liccardo Gennaro13,Oh Jinwon4,Stone Michael L.1,McShane Eric J.1ORCID,Werghi Baraa135,Nathan Sindhu1,Song Chengyu6,Ciston Jim6ORCID,Bustillo Karen C.6,Hoffman Adam S.5,Hong Jiyun5,Perez‐Aguilar Jorge5,Bare Simon R.5,Cargnello Matteo13ORCID

Affiliation:

1. Department of Chemical Engineering Stanford University Stanford California 94305 United States

2. Applied Physics and Materials Science California Institute of Technology Pasadena California 91125 United States

3. SUNCAT Center for Interface Science and Catalysis Stanford University Stanford California 94305 United States

4. Department of Materials Science and Engineering Stanford University Stanford California 94305 United States

5. SLAC National Accelerator Laboratory 2575 Sand Hill Road Menlo Park California 94305 United States

6. National Center for Electron Microscopy Facility Molecular Foundry Lawrence Berkeley National Lab Berkeley California 94720 United States

Abstract

AbstractMulticomponent catalysts can be designed to synergistically combine reaction intermediates at interfacial active sites, but restructuring makes systematic control and understanding of such dynamics challenging. We here unveil how reducibility and mobility of indium oxide species in Ru‐based catalysts crucially control the direct, selective conversion of CO2 to ethanol. When uncontrolled, reduced indium oxide species occupy the Ru surface, leading to deactivation. With the addition of steam as a mild oxidant and using porous polymer layers to control In mobility, Ru−In2O3 interface sites are stabilized, and ethanol can be produced with superior overall selectivity (70 %, rest CO). Our work highlights how engineering of bifunctional active ensembles enables cooperativity and synergy at tailored interfaces, which unlocks unprecedented performance in heterogeneous catalysts.

Publisher

Wiley

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