Synthesis of High Metal Loading Single Atom Catalysts and Exploration of the Active Center Structure
Abstract
Single-atom catalysts (SACs) have been rising recently as a new frontier in the catalysis field. Due to maximum atom utilization efficiency and tunable electronic structures, SACs exhibit highly distinctive catalytic performance from bulk counterparts. SACs with high metal loading will facilitate practical applications. To that end, this Review focuses on recent strategies to maximize metal loading. An appropriate substrate, mainly heteroatom-doped carbon materials, is the key to avoiding aggregation or sintering during synthetic procedures. The coordination site construction and spatial confinement strategies are adopted to prepare SACs with high metal loading. Advanced characterization techniques with atomic resolution are indispensable for identification of the exact structure of SACs. This is true, especially for the applications and challenges in developing in situ/operando characterization techniques at the atomic level, which are discussed in this Review. Moreover, it is fundamentally necessary to investigate the active center structure, which facilitates any design of efficient SACs that can maximize single-atom catalytic activity. Furthermore, this Review highlights challenges and prospects for development of SACs.
Recommended Citation
K. Wang et al., "Synthesis of High Metal Loading Single Atom Catalysts and Exploration of the Active Center Structure," ChemCatChem, vol. 13, no. 1, pp. 28 - 58, Wiley-VCH Verlag, Jan 2021.
The definitive version is available at https://doi.org/10.1002/cctc.202001255
Department(s)
Chemical and Biochemical Engineering
Research Center/Lab(s)
Intelligent Systems Center
Keywords and Phrases
Active center analysis; High metal loading; In situ characterization; Single-atom catalysts; Synthesis strategies.
International Standard Serial Number (ISSN)
1867-3880; 1867-3899
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2021 Wiley, All rights reserved.
Publication Date
12 Jan 2021
Comments
National Science Foundation, Grant NSF 1803812