X射线光电子能谱
催化作用
氮氧化物
化学
化学气相沉积
红外光谱学
傅里叶变换红外光谱
选择性催化还原
漫反射红外傅里叶变换
离解(化学)
合金
程序升温还原
无机化学
分析化学(期刊)
核化学
化学工程
物理化学
有机化学
燃烧
光催化
工程类
作者
Eunji Cho,Seung-Ik Kim,Dong‐Won Lee,Young-Woo You,Mintaek Im,Soo Min Kim,Iljeong Heo,Jungkyu Choi,Young Jin Kim,Jin Hee Lee
标识
DOI:10.1016/j.apsusc.2022.155545
摘要
In previous studies IrRu/Al2O3 has exhibited good activity for NOx reduction by CO at low temperature. The Ir-Ru alloy structure was revealed to be the origin of the outstanding activity of IrRu/Al2O3 in the CO-induced deNOx reaction. In this work, preferential chemical vapor deposition (pCVD) was applied as an effective and selective Ir-Ru alloy catalyst synthesis method, which selectively deposits Ir precursor on the pre-existing Ru nanoparticles. The synthesized IrRu/Al2O3 catalysts were characterized by transmission electron microscopy, X-ray diffraction, X-ray absorption spectroscopy, temperature programmed reduction, X-ray photoelectron spectroscopy, and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTs) analyses. The results confirmed the formation of Ir-Ru alloy, and showed that Ir can be preferentially deposited on Ru surface via pCVD, rather than on the Al2O3 support. IrRu/Al2O3 synthesized by pCVD exhibited better performance in the NOx reduction by CO than catalysts prepared by the conventional impregnation method. Its catalytic activity varied with Ir content, which was precisely controllable using pCVD. The investigation of catalyst surface by DRIFT revealed that the accelerated NO dissociation is the primary reason for its excellent low-temperature activity of the IrRu/Al2O3 catalyst prepared by pCVD.
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