Journal
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING
Volume 64, Issue 3, Pages 491-532Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/01614940.2020.1821443
Keywords
Single atom; CO oxidation; metal-support interaction; defects; electronic structure
Categories
Funding
- National Science Foundation [CMMI-1661699]
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Single-atom catalysts (SACs) have attracted significant attention due to their high atom utilization and excellent catalytic activities. This review discusses the design principles, synthesis methods, and the influence of metal-support interactions on the activity of SACs for CO oxidation. Moreover, the CO oxidation mechanisms over SACs are evaluated and the future research directions and challenges for SAC-catalyzed CO oxidation are outlined.
Single-atom catalysts (SACs) have received boosting attention due to their high atom utilization and incredible activities in a wide range of catalytic processes. Numerous SACs have been investigated for CO oxidation both experimentally and theoretically, including noble-metal catalysts (Pt, Au, Pd, etc.) and non-noble-metal catalysts (Fe, Co, Ni, etc.), in which the atomically dispersed metal atoms are anchored on supports via strong metal-support interactions. This unique structure of SACs contributes to activating the adsorbed CO and O(2)and stabilizing the intermediates. Electron transfer between the metal atom and the support plays an important role in tuning the electronic structure, which can greatly influence the activity, selectivity, and stability of SACs. In this review, the design principles and synthesis methods of SACs for CO oxidation are discussed with emphasis on single-atom active sites and metal-support interactions. Four CO oxidation mechanisms over SACs are evaluated. Moreover, the challenges and future research directions for SAC-catalyzed CO oxidation are outlined.
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