Activity and Selectivity Trends in Synthesis Gas Conversion to Higher Alcohols

• Published in: Topics in catalysis Vol. 57; no. 1-4; pp. 135 - 142
• Main Authors: Medford, Andrew J., Lausche, Adam C., Abild-Pedersen, Frank, Temel, Burcin, Schjødt, Niels C., Nørskov, Jens K., Studt, Felix
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.02.2014
• Subjects: Catalysis; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Industrial Chemistry/Chemical Engineering; OriginalPaper; Pharmacy; Physical Chemistry; Micro-kinetic modeling; Density functional theory; Higher alcohols; Synthesis gas conversion
• ISSN: 1022-5528; 1572-9028
• DOI: 10.1007/s11244-013-0169-0

Production of higher alcohols directly from synthesis gas is an attractive chemical process due to the high value of alcohols as fuel blends and the numerous possibilities for production of synthesis gas. Despite years of research the industrial viability of such a process is severely limited due to lack of suitable catalysts. In this work we contribute to an understanding why it has been difficult to find transition-metal higher alcohol catalysts, and point to possible strategies for discovering new active and selective catalysts. Our analysis is based on extensive density functional theory calculations to determine the energetics of ethanol formation on a series of metal (211) surfaces. The energetic information is used to construct a mean-field micro-kinetic model for the formation of ethanol via CH x –CO coupling. The kinetic model is used along with a descriptor-based analysis to gain insight into the fundamental factors determining activity and selectivity on transition-metal surfaces.