Recent advances in single-atom catalysts for CO oxidation

Haotian Zhang, Siyuan Fang, Y. Hu
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引用次数: 33

Abstract

ABSTRACT 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 O2 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.
一氧化碳氧化单原子催化剂的研究进展
单原子催化剂(SACs)由于其高原子利用率和在广泛的催化过程中令人难以置信的活性而受到越来越多的关注。许多SACs已经被研究用于CO氧化的实验和理论,包括贵金属催化剂(Pt, Au, Pd等)和非贵金属催化剂(Fe, CO, Ni等),其中原子分散的金属原子通过强金属-载体相互作用锚定在载体上。SACs的这种独特结构有助于活化吸附的CO和O2,并稳定中间体。金属原子与载体之间的电子转移对电子结构的调整起着重要的作用,这对SACs的活性、选择性和稳定性有很大的影响。本文综述了用于CO氧化的SACs的设计原则和合成方法,重点讨论了单原子活性位点和金属-载体相互作用。评估了sac上的四种CO氧化机制。展望了sac催化CO氧化技术面临的挑战和未来的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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