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亚硝酸甲酯在多晶钯表面上吸附的光电子能谱 被引量:2
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作者 张训生 鲍德松 +1 位作者 杜志强 董峰 《真空科学与技术》 CSCD 1995年第1期7-13,共7页
通过对低温和室温下的钯表面吸附亚硝酸甲酯的角分辨紫外光电子能谱(UPS)的分析,以及对亚硝酸甲酯(CH3ONO)分子的abinitio理论计算,讨论了UPS的几个港峰对应轨道的性质,并对照相应能缓的分子轨道组成和Mulliken集居数分析,提出... 通过对低温和室温下的钯表面吸附亚硝酸甲酯的角分辨紫外光电子能谱(UPS)的分析,以及对亚硝酸甲酯(CH3ONO)分子的abinitio理论计算,讨论了UPS的几个港峰对应轨道的性质,并对照相应能缓的分子轨道组成和Mulliken集居数分析,提出在低温下CH3ONO主要是通过中心氧原子与Pd的d轨道相互作用而吸附的。与NO和CO共吸附峰相比较,则认为在室温下亚硝酸甲酯分解为NO和CO等的共吸附。本工作有助于亚硝酸乙酯与CO在Pd/Al2O3上气相催化合成草酸二乙酯机理的理解。 展开更多
关键词 甲硝酸甲酯 吸附 光电子能谱 多晶钯 催化剂
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多晶钯表面上CO脱附动力学的探讨
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作者 翟润生 向宁 +1 位作者 刘宪春 郭燮贤 《分子催化》 EI CAS CSCD 1989年第3期190-196,共7页
本文研究了多晶钯表面上CO脱附动力学,对各种覆盖度的脱附谱图进了划分温区的分析,对低温区首次提出恒定脱附速度的动力学解析.对于多晶钯面上CO的脱附,随脱附温度的升高,脱附反应级数减小而视活化能增加.为解释这种现象提出了活性集团... 本文研究了多晶钯表面上CO脱附动力学,对各种覆盖度的脱附谱图进了划分温区的分析,对低温区首次提出恒定脱附速度的动力学解析.对于多晶钯面上CO的脱附,随脱附温度的升高,脱附反应级数减小而视活化能增加.为解释这种现象提出了活性集团假设,深入研究活性集团的动力学性能将有助于了解脱附过程的动力学特性. 展开更多
关键词 多晶钯 CO 脱附动力学
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Determination of the Real Surface Area of Palladium Electrode 被引量:1
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作者 方兰兰 陶骞 +3 位作者 李明芳 廖玲文 陈栋 陈艳霞 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2010年第5期543-548,621,共7页
Four methods, including voltammetric measurement of double layer capacitance, surface oxides reduction, under potential deposition of Cu and carbon monoxide (CO) stripping have been applied to evaluate the real surf... Four methods, including voltammetric measurement of double layer capacitance, surface oxides reduction, under potential deposition of Cu and carbon monoxide (CO) stripping have been applied to evaluate the real surface area of a polycrystalline Pd (pc-Pd) electrode. The results reveal that the second and third methods lead to consistent results with deviations below 5%. And from the determined double layer capacitance and CO stripping charge, it is deduced that the double layer capacity unit area is 23.1±0.4μF/cm2 and the saturated CO adlayer should be ca. 0.66 ML in order to ensure that the real surface area as determined is consistent with the other two techniques. The applicability as well as the attentions when applying these techniques for the determination of the real surface area of pc-Pd electrodes have been discussed. 展开更多
关键词 Polycrystalline Pd electrode Real surface area Double layer capacitance Oxygen adsorption Under potential deposition CO stripping
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Preparation and electro-catalytic activity of nanoporous palladium by dealloying rapidly-quenched Al_(70)Pd_(17)Fe_(13) quasicrystalline alloy 被引量:4
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作者 Xin-yi LIU Ying-min WANG +4 位作者 Jian-bing QIANG Bao-lin WANG Dian-guo MA Wei ZHANG Chuang DONG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2019年第4期785-790,共6页
The formation of nanoporous Pd was studied by electro-chemical dealloying a rapidly-quenched Al70Pd17Fe13 quasicrystal alloy in dilute NaCl aqueous solution,and the electro-catalytic activity of the nanoporous Pd towa... The formation of nanoporous Pd was studied by electro-chemical dealloying a rapidly-quenched Al70Pd17Fe13 quasicrystal alloy in dilute NaCl aqueous solution,and the electro-catalytic activity of the nanoporous Pd towards methanol electro-oxidation was evaluated by cyclic voltammetry in 1 mol/L KOH solution.XRD and TEM analyses revealed that nano-decomposition of quasicrystal grains occurred in the initial stage of dealloying,and the fully dealloyed sample was composed of FCC-Pd phase.Scanning electron microscopy observation indicated that a maze-like nanoporous pattern was formed in the dealloyed sample,consisting of percolated pores of 5.20 nm in diameter in a skeleton of randomly-orientated Pd nano-ligaments with a uniform thickness of^5 nm.A retention of^12 at.%Al in the Pd nano-ligments was determined by energy dispersive X-ray spectroscopy(EDS).The nanoporous Pd demonstrated obvious electro-catalytic activity towards methanol electro-oxidation in alkaline environment. 展开更多
关键词 nanoporous palladium Al-Pd-Fe quasicrystal DEALLOYING electro-catalytic activity
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