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通过原位金属有机模板转化增强 Pt-CoO 催化剂对甲苯的催化燃烧。

Enhancement of catalytic toluene combustion over Pt-CoO catalyst through in-situ metal-organic template conversion.

机构信息

School of Environment and Energy, South China University of Technology, 510006 Guangzhou, China.

School of Environment and Energy, South China University of Technology, 510006 Guangzhou, China; National Engineering Laboratory for VOCs Pollution Control Technology and Equipment (SCUT), 510006 Guangzhou, China; Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control (SCUT), 510006 Guangzhou, China; Guangdong Provincial Engineering and Technology Research Centre for Environmental Risk Prevention and Emergency Disposal (SCUT), 510006 Guangzhou, China.

出版信息

Chemosphere. 2021 Jan;262:127738. doi: 10.1016/j.chemosphere.2020.127738. Epub 2020 Jul 21.

Abstract

A Pt-CoO catalyst named Pt-Co(OH)-O was prepared by metal-organic templates (MOTs) conversion and used for catalytic oxidation of toluene. Through the conversion, the morphology of catalysts transformed from rhombic dodecahedron to nanosheet and the coated Pt nanoparticles (NPs) were more exposed. The Binding energy shift in XPS test indicates that the strong metal-support strong interaction (SMSI) has enhanced, and the physicochemical changes caused by it are characterized by other techniques. At the same time, Pt-Co(OH)-O showed the best catalytic performance (T = 157 °C, T = 167 °C, E = 40.85 kJ mol, TOF = 2.68 × 10 s) and good stability. In addition, the in situ Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) studies have shown that because SMSI weakened the Co-O bond, the introduction of Pt NPs can make the migration of oxygen in the catalyst easier. The change of binding energy change and the content of various species in the quasi in situ XPS experiment further confirmed that the Pt-Co(OH)-O catalyst has stronger SMSI, resulting in its stronger electron transfer ability and oxygen migration ability, which is conducive to catalytic reactions. This work provides new ideas for the development of supported catalysts and provides a theoretical reference for the relevant verification of SMSI.

摘要

一种名为 Pt-Co(OH)-O 的 Pt-CoO 催化剂通过金属有机模板 (MOTs) 转化制备,并用于催化氧化甲苯。通过这种转化,催化剂的形态从菱形十二面体转变为纳米片,并且覆盖的 Pt 纳米颗粒 (NPs) 更加暴露。XPS 测试中的结合能位移表明,强金属-载体强相互作用 (SMSI) 得到了增强,并且由其引起的物理化学变化通过其他技术进行了表征。同时,Pt-Co(OH)-O 表现出最佳的催化性能 (T = 157°C,T = 167°C,E = 40.85 kJ mol,TOF = 2.68×10 s) 和良好的稳定性。此外,原位漫反射红外傅里叶变换光谱 (DRIFTS) 研究表明,由于 SMSI 削弱了 Co-O 键,Pt NPs 的引入可以使催化剂中氧的迁移更容易。准原位 XPS 实验中结合能变化和各种物种含量的变化进一步证实了 Pt-Co(OH)-O 催化剂具有更强的 SMSI,从而使其具有更强的电子转移能力和氧迁移能力,这有利于催化反应。这项工作为负载型催化剂的发展提供了新思路,并为 SMSI 的相关验证提供了理论参考。

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