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Updated: Sep 17, 2026

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Alumina-Supported Single-Atom Catalysts: Rational Design, Synthesis Strategies, and Functional Applications
Krishnaveni S Binu1,2, Muhammed Shanif1,2, Jubi John1,2
1Chemical Sciences and Technology Division, CSIR-National Institute for Interdisciplinary Science and Technology (CSIR-NIIST), Thiruvananthapuram, India.
Abstract:
Support materials determine the stability and electronic characteristics of active metal sites, offering a foundation for customizing heterogeneous catalysts for specific functional applications. Alumina (Al2O3) is an irreducible oxide and an excellent support material in industrial catalysts because of its exceptional thermal stability, structural versatility, and affinity for metal anchoring and molecule adsorption. Isolated metal atoms having unique electronic structure enable 100% atom utilization efficiency and represent the cornerstone of single atom catalysts (SACs). Although the concept of SACs has advanced drastically, SACs on Al2O3 supports remain a relatively nascent area of research. This review systematically examines the landscape of SACs supported on Al2O3, assessing the synthetic strategies employed, expounding their structural characteristics, metal-support interactions, and applications. Commencing with an overview of the various transitional phases of Al2O3, we explore the critical role of surface defects and penta-coordinated Al3+ sites in coordinating and stabilizing metal atoms. Furthermore, we correlate these structural features to their catalytic performance, elucidated through advanced characterization techniques such as X-ray absorption spectroscopy and atomic-resolution electron microscopy. Through a comprehensive discussion, the review attempts to provide a clear and systematic explanation of the current accomplishments, obstacles, and future prospects in the emerging research field of single-atom catalysis.
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