The catalytic oxidation of volatile organic compounds(VOCs)is of considerable significance for the sustainable development of the chemical industry;thus,considerable efforts have been devoted to the exploration of eff...The catalytic oxidation of volatile organic compounds(VOCs)is of considerable significance for the sustainable development of the chemical industry;thus,considerable efforts have been devoted to the exploration of efficient catalysts for use in this reaction.In this regard,the development and utilization of single-atom catalysts(SACs)in VOCs decomposition is a rapidly expanding research area.SACs can be employed as potential catalysts for oxidizing VOC molecules due to their optimal utilization efficiency,unique atomic bonding structures,and unsaturated orbits.Progress has been achieved,while the challenges surrounding precise regulation of the microstructures of SACs for improving their low-temperature efficiency,stability,and product selectivity under practical conditions are remaining.Therefore,elucidating structure-performance relationships and establishing intrinsic modulating mechanisms are urgently required for guiding researchers on how to synthesize effective and stable functional SACs proactively.Herein,recent advances in the design and synthesis of functional SACs for application in the catalytic oxidation of VOCs are summarized.The experimental and theoretical studies revealing higher efficiency,stability,and selectivity of as-prepared functional SACs are being highlighted.Accordingly,the future perspectives in terms of promising catalysts with multi-sized composite active sites and the illustration of intrinsic mechanism are proposed.The rapid intelligent screening of applicable SACs and their industrial applications are also discussed.展开更多
基金financially supported by the National Natural Science Foundation of China(Nos.22276145,2187613921922606)+1 种基金National Key R&D Program of China(No.2022YFB4101500)China Postdoctoral Science Foundation(No.2023M732783)。
文摘The catalytic oxidation of volatile organic compounds(VOCs)is of considerable significance for the sustainable development of the chemical industry;thus,considerable efforts have been devoted to the exploration of efficient catalysts for use in this reaction.In this regard,the development and utilization of single-atom catalysts(SACs)in VOCs decomposition is a rapidly expanding research area.SACs can be employed as potential catalysts for oxidizing VOC molecules due to their optimal utilization efficiency,unique atomic bonding structures,and unsaturated orbits.Progress has been achieved,while the challenges surrounding precise regulation of the microstructures of SACs for improving their low-temperature efficiency,stability,and product selectivity under practical conditions are remaining.Therefore,elucidating structure-performance relationships and establishing intrinsic modulating mechanisms are urgently required for guiding researchers on how to synthesize effective and stable functional SACs proactively.Herein,recent advances in the design and synthesis of functional SACs for application in the catalytic oxidation of VOCs are summarized.The experimental and theoretical studies revealing higher efficiency,stability,and selectivity of as-prepared functional SACs are being highlighted.Accordingly,the future perspectives in terms of promising catalysts with multi-sized composite active sites and the illustration of intrinsic mechanism are proposed.The rapid intelligent screening of applicable SACs and their industrial applications are also discussed.
基金supported by the National Natural Science Foundation of China (51072096)the National Basic Research Program of China (973 Program,2010CB732304)the National High Technology Research and Development Program of China (863 Program,2013AA065302)~~
文摘通过在Ce0.6Zr0.4O2载体上浸渍Pt(NO3)2制得Pt/Ce0.6Zr0.4O2催化剂,该催化剂在松散接触条件下,于NO + O2或O2气氛中均表现出比Pt/Al2O3更好的碳烟氧化性能.进一步研究表明,Pt/Ce0.6Zr0.4O2催化剂中的Pt与Ce0.6Zr0.4O2存在相互作用,使得催化剂在一定温度范围内对活性氧的利用率大为提高,从而促进了气氛中NO ? NO2的循环,乃至碳烟与NO2的反应和碳烟表面含氧中间物种的生成;更重要的是,这部分活性氧本身可加速含氧中间物种的分解.因此,在NO + O2的气氛中,Pt/Ce0.6Zr0.4O2催化剂的碳烟起燃温度比Pt/Al2O3降低了34 °C.