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不同环境条件下二氧化氮在金属氧化物颗粒表面吸附的X射线光电子能谱研究

XPS study of nitrogen dioxide adsorption on metal oxide particle surfaces under different environmental conditions.

作者信息

Baltrusaitis Jonas, Jayaweera Pradeep M, Grassian Vicki H

机构信息

Department of Chemistry, University of Iowa, Iowa City, IA 52242, USA.

出版信息

Phys Chem Chem Phys. 2009 Oct 1;11(37):8295-305. doi: 10.1039/b907584d. Epub 2009 Jul 2.

Abstract

The adsorption of nitrogen dioxide on gamma aluminium oxide (gamma-Al(2)O(3)) and alpha iron oxide (alpha-Fe(2)O(3)) particle surfaces under various conditions of relative humidity, presence of molecular oxygen and UV light has been investigated. X-Ray photoelectron spectroscopy (XPS) is used to monitor the different surface species that form under these environmental conditions. Adsorption of NO(2) on aluminum oxide particle surfaces results primarily in the formation of surface nitrate, NO(3)(-) with an oxidation state of +5, as indicated by a peak with binding energy of 407.3 eV in the N1s region. An additional minority species, sensitive to the presence of relative humidity and molecular oxygen, is also observed in the N1s region with lower binding energy of 405.9 eV. This peak is assigned to a surface species in the +4 oxidation state. When irradiated with UV light, other species form on the surface. These surface-bound photochemical products all have lower binding energy, between 400 and 402 eV, indicating reduced nitrogen species in the range of N oxidations states spanning +1 to -1. Co-adsorbed water decreases the amount of these reduced surface-bound products while the presence of molecular oxygen completely suppresses the formation of all reduced nitrogen species on aluminum oxide particle surfaces. For NO(2) on iron oxide particle surfaces, photoreduction is enhanced relative to gamma-Al(2)O(3) and surface bound photoreduced species are observed under all environmental conditions. Complementing the experimental data, N1s core electron binding energies (CEBEs) were calculated using DFT for a number of nitrogen-containing species in the gas phase and adsorbed on an Al(8)O(12) cluster. A range of CEBEs is calculated for various nitrogen species in different adsorption modes and oxidation states. These calculated values are discussed in light of the peaks observed in the XPS N1s region and the possible species that form following NO(2) adsorption and photoreaction on metal oxide particle surfaces under different conditions of relative humidity, presence of molecular oxygen and UV light.

摘要

研究了在不同相对湿度、分子氧存在和紫外光条件下,二氧化氮在γ-氧化铝(γ-Al₂O₃)和α-氧化铁(α-Fe₂O₃)颗粒表面的吸附情况。采用X射线光电子能谱(XPS)监测在这些环境条件下形成的不同表面物种。二氧化氮在氧化铝颗粒表面的吸附主要导致形成表面硝酸盐NO₃⁻,其氧化态为+5,这由N1s区域中结合能为407.3 eV的峰表明。在N1s区域还观察到另一种对相对湿度和分子氧的存在敏感的少数物种,其结合能较低,为405.9 eV。该峰归属于氧化态为+4的表面物种。当用紫外光照射时,表面会形成其他物种。这些表面结合的光化学产物的结合能都较低,在400至402 eV之间,表明氮的氧化态在+1至-1范围内的还原态物种。共吸附的水会减少这些还原态表面结合产物的量,而分子氧的存在则完全抑制了氧化铝颗粒表面所有还原态氮物种的形成。对于二氧化氮在氧化铁颗粒表面的情况,相对于γ-Al₂O₃,光还原作用增强,并且在所有环境条件下都观察到表面结合的光还原物种。作为实验数据的补充,使用密度泛函理论(DFT)计算了气相中以及吸附在Al₈O₁₂簇上的多种含氮物种的N1s核心电子结合能(CEBEs)。针对不同吸附模式和氧化态的各种氮物种计算了一系列CEBEs。根据在XPS N1s区域观察到的峰以及在不同相对湿度、分子氧存在和紫外光条件下二氧化氮吸附和光反应后在金属氧化物颗粒表面可能形成的物种,对这些计算值进行了讨论。

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