首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Support-Induced Effects of LaFeO3 Perovskite on the Catalytic Performances of Supported Pt Catalysts in DeNO_x Applications
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Support-Induced Effects of LaFeO3 Perovskite on the Catalytic Performances of Supported Pt Catalysts in DeNO_x Applications

机译:LaFeO3钙钛矿对DeNO_x应用中负载的Pt催化剂催化性能的支持诱导效应

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A comparative investigation of the catalytic performance in the simultaneous conversion of NO_x and N2O has been achieved on supported nanosized Pt particles interacting with conventional alumina and perovskite based materials. Particular attention has been paid to successive thermal treatments under reductive and oxidative atmospheres which induce bulk and surface reconstructions. Those modifications considerably alter the catalytic behavior of Pt in interaction with LaFeO3 or γ-Al2O3 in terms of activity and selectivity toward the selective transformation of NO_x to nitrogen at low temperature. Changes in physico-chemical properties have been examined using appropriate techniques, such as H2-temperature-programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and Fourier transform infrared (FTIR) of CO adsorption. It has been found that oxidic Pt~(4+) species initially stabilized on LaFeO3 lead after subsequent H2 reduction to the formation of metallic nano-Pt particles in stronger interaction than on γ-Al2O3 support and then become more resistant to sintering during thermal aging in 1000 ppm NO, 1000 ppm N2O,3 vol % O2, 0.5 vol % H2O, and 0.5 vol % H2 at 500 °C Correlatively, significant improvements have been observed in the selective reduction of NO_x to nitrogen. This study opens new prospects in the development of supported catalysts containing low Pt loadings because of the existence of stronger interactions with perovskite supports.
机译:在与常规氧化铝和钙钛矿基材料相互作用的负载纳米级Pt颗粒上,已经完成了NO_x和N2O同时转化中催化性能的比较研究。特别引起人们注意的是在还原性和氧化性气氛下进行的连续热处理,这些热处理会引起整体和表面重建。这些修饰极大地改变了Pt与LaFeO3或γ-Al2O3相互作用的催化行为,这在活性和选择性方面有利于低温下NO_x选择性转化为氮。已使用适当的技术,例如CO的H2温度程序化还原(TPR),X射线光电子能谱(XPS),透射电子显微镜(TEM)和傅里叶变换红外(FTIR),检查了物理化学性质的变化吸附。已经发现,氧化的Pt〜(4+)物种最初稳定在LaFeO3铅上,随后被H2还原,形成了比在γ-Al2O3载体上更强的相互作用的金属纳米Pt颗粒,然后在热时效过程中变得更耐烧结在500°C的1000 ppm NO,1000 ppm N2O,3%体积%的O2、0.5%体积的H2O和0.5%体积的H2中,相对地,已观察到将NO_x选择性还原为氮的重大改进。由于与钙钛矿载体之间存在较强的相互作用,这项研究为含低Pt负载的载体催化剂的开发开辟了新的前景。

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