The correlation between the inclination of surface reaction sites and the spatial distribution of desorbing product molecules
The correlation between the inclination of surface reaction sites and the spatial distribution of desorbing product molecules
批准号:
03640419
负责人:
MATSUSHIMA Tatsuo
金额:
$1.28万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1991
资助国家:
日本
项目状态:
已结题
起止时间:
1991 至 1993
中文摘要
1.本课题以反应位的倾斜为重点,在Pt(110)(1x 2)台阶表面上测量了CO氧化脱附产物CO_2的空间分布。(阶地的倾斜角度:35.2度)、Ir(110)(1x 2)(35.2度)、Pt(112)(19.5度)、Pt(335)(14.4度)和Pt(557)(9.5度),以检查倾斜度在空间分布中保持的准确程度。在空间分布上,该角度已被证实保持在约85%。这意味着空间分布测量对于识别反应位点是有力的。随着反应覆盖率的增加,在上述台阶表面上加热CO和O2的粘合层所引起的CO_2生成扩展到较低的温度,在150-400 K范围内产生多个峰,并分别分析了各峰的空间分布和速度分布。CO_2解吸的平动温度在解吸角最大时达到最大值,随着解吸角的增大,平动温度迅速降低。这表明了空间分布被锐化的机制,即,解吸产物的速度分量在反应位点的法线方向上增强.随着反应物覆盖率的增加,反应位点由平台向台阶或沟槽扩展。在高覆盖度下,未在阶地法线中准直的解吸分量增加。
英文摘要
1. In this project focused on the inclination of the reaction sites, the spatial distributions of desorbing product CO_2 in the CO oxidation are measured on several stepped platinum surfaces, Pt(110)(1x2)(the inclining angle of terraces : 35.2゚), Ir(110)(1x2)(35.2゚), Pt(112)(19.5゚), Pt(335)(14.4゚) and Pt(557)(9.5゚), to examine how accurately the inclination is preserved in the spatial distributions. The angle has been confirmed to be preserved to about 85% in the spatial distribution. This means that the spatial distribution measurements are powerful to identify reaction sites.2. The CO_2 formation induced by heating the coadlayr of CO and oxygen on the stepped surfaces mentioned above is extended to lower temperatures, with increasing the reaction coverages, yielding several peaks in the range of 150-400 K.The spatial and velocity distributions of each peak have been separately analyzed. The translational temperature of desorbing CO_2 is maximized at the desorption angle where the flux is maximized and decreases quickly with increasing the shift of the angle. This indicates the mechanism in which the spatial distribution is sharpened, i.e., the velocity component of desorbing product is enhanced in the normal direction of the reaction sites.3. The reaction sites are extended from the terraces to steps or into surface troughs when the reactant coverages are increased. The desorption component not collimated in the terrace normal is increased at high coverages.
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T.Matsushima: "Transformation of Ir(110)(1x1)into(1x2)and spatial distribution of reactive carbon dioxide desorption." Journal of Chemical Physics.94. 704-710 (1991)
T.Matsushima:“Ir(110)(1x1) 到 (1x2) 的转化以及反应性二氧化碳解吸的空间分布。”
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Y.Ohno: "Desorption,dissociation and orientation of oxygen admolecules on a reconstructed platinum(110)(1×2)surface studied by thermal desorption and near-edgeX-ray-absorption fine-structure." Japanese Journal of Applied Physics. 32. 383-385 (1993)
Y.Ohno:“通过热解吸和近边缘 X 射线吸收精细结构研究重建铂 (110)(1×2) 表面上氧分子的解吸、解离和取向”,《日本应用物理学杂志》32。 .383-385 (1993)
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T.Matsushima: "Velocity distribution of desorbing product in carbon monoxide oxidation on palladium(110)." J.Molecular Catalysis. 72. 169-174 (1992)
T.Matsushima:“钯 (110) 上一氧化碳氧化中解吸产物的速度分布。”
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Y.Ohno: "Reaction diagram of carbon monoxide and oxygen on palladium(100) and angular distribution of reactive carbon dioxide desorption." Surface Science. 273. 291-300 (1992)
Y.Ohno:“一氧化碳和氧气在钯(100)上的反应图以及反应性二氧化碳解吸的角分布。”
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Y.Ohno: "Orientation of oxygen admolecules on a platinum(110)(1x2) reconstructed surface ; Near-edge X-ray absorption fine structure study." Surface Science. 275. 281-289 (1992)
Y.Ohno:“铂 (110)(1x2) 重建表面上氧分子的取向;近边缘 X 射线吸收精细结构研究。”
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共 24 条
Direct assignment of active nitrous oxide from spatial distributions of emitted products
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批准号:21550004
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.08万
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财政年份:2009
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负责人:MATSUSHIMA Tatsuo
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依托单位:
Peculiar nitrogen desorption on rhodium surfaces and the decomposition mechanism of nitrogen oxides
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批准号:13640493
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$0.51万
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财政年份:2001
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负责人:MATSUSHIMA Tatsuo
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依托单位:
Assignment and identification of reaction sites on solid surfaces
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批准号:06403012
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$14.53万
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财政年份:1994
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负责人:MATSUSHIMA Tatsuo
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依托单位: