Journal
CATALYSIS SCIENCE & TECHNOLOGY
Volume 8, Issue 14, Pages 3428-3449Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cy00608c
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Funding
- China Scholarship Council [201704910592]
- Chinese Academy of Sciences [XDA07070200, XDA09030102]
- Science Foundation of Fujian Province [2006l2005]
- Science Foundation of Guizhou Province [[2018]2193]
- Fujian industrial guide project [2016H0048]
- NSF of China [21703247]
- University of Wyoming
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The quickly increasing demand for sustainable energy and materials requires researchers to develop highly efficient and stable catalytic materials for the hydrogenation of carbon-oxygen bonds into chemicals and fuels. Cu-based catalysts have been attracting tremendous attention in gas-phase catalytic reactions, such as the water-gas shift, CO oxidation and NOx reduction reactions. In particular, the C-O bond hydrogenation reaction is an economical and environmentally friendly way to produce alcohols. However, the instability of Cu-based catalysts has become a great challenge for industrial application. The majority of publications discuss the instability of Cu-based catalysts for reactions involving the hydrogenation of dimethyl oxalate, methyl acetate, furfural, or CO2 to alcohols. This review briefly summarizes the roots of Cu-based catalyst deactivation and introduces five strategies for improving their stability, as well as the evolution of copper species during preparation and reaction and a novel Cu-based catalyst technology.
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