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Thermal and photon induced reactions of vinyl chloride adsorbed on Ag(111).

机译:氯乙烯在Ag(111)上的热和光子诱导反应。

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Vinyl Chloride physisorbs on liquid nitrogen cooled Ag(111). Thermal Desorption Spectroscopy (TDS) indicates that most of the monolayer desorbs molecularly at 119 K in a first order process with desorption activation energy of 6.7 kcal/mol. The multilayer desorbs molecularly at 92 K in a first order process with desorption activation energy of 4.3 kcal/mol. High Resolution Electron Energy Loss Spectroscopy (HREELS) indicates that the monolayer vinyl chloride is adsorbed with the molecular plane approximately parallel to the Ag(111) surface plane. TDS and HREELS indicate that as the Ag(111) surface is heated to temperatures greater than 126 K, small quantities of the physisorbed vinyl chloride monolayer dissociate into adsorbed vinyl and Cl. Further heating to temperatures greater than 180 K results in vinyl and Cl recombination with subsequent molecular desorption in a second order process with a desorption activation energy of 10.7 kcal/mol.; Pulsed ultraviolet laser irradiation of the monolayer results in desorption and dissociation through a substrate mediated, electron transfer mechanism. The calculated photon excited, substrate electron energy required for vertical attachment is 4.03 eV above the Fermi level while the experimental photon energy threshold is 3.49 eV. The vinyl chloride photodissociation products are vinyl and Cl. Upon heating the substrate, two adsorbed vinyl species combine on the Cl-Ag(111) surface at 249 K to produce 1,3 butadiene in a first order process with a desorption activation energy of 10.4 kcal/mol. The proposed bi-molecular reaction mechanism indicates adsorbed vinyl surface diffusion determines the rate of 1,3-butadiene formation.; Pre-adsorbed Cl on the Ag(111) surface causes physisorbed vinyl chloride to desorb at 150 K in TDS. In addition, pre-adsorbed Cl-Ag(111) increases substrate electron energy required for vertical attachment and hence decreases the photochemical dissociation cross-section. HREELS indicates that physisorbed vinyl chloride on the Cl-Ag(111) surface has its molecular plane even more parallel to the surface plane than for the case of no pre-adsorbed Cl and that the vinyl chloride "hydrogen bonds" to the Cl-Ag(111).
机译:氯乙烯会物理吸附在液氮冷却的Ag(111)上。热脱附谱(TDS)表明,大多数单层分子在一级反应中以119 kK / mol的解吸活化能在119 K下分子脱附。该多层在一级反应中以92 k K / mol的解吸活化能在92 K下进行分子解吸。高分辨率电子能量损失谱(HREELS)表明,单层氯乙烯的分子平面近似平行于Ag(111)表面平面。 TDS和HREELS表明,随着将Ag(111)表面加热到大于126 K的温度,少量的物理吸附的氯乙烯单层解离成吸附的乙烯基和Cl。进一步加热到高于180 K的温度会导致乙烯基和Cl重组,随后在第二级过程中发生分子解吸,解吸活化能为10.7 kcal / mol。单层的脉冲紫外激光辐照导致通过底物介导的电子转移机理解吸和解离。计算得到的垂直附着所需的光子激发的衬底电子能量比费米能级高4.03 eV,而实验光子能量阈值为3.49 eV。氯乙烯光解离产物是乙烯基和Cl。加热基材后,两种吸附的乙烯基物质在249 K的Cl-Ag(111)表面结合,在一级过程中以10.4 kcal / mol的解吸活化能生成1,3丁二烯。提出的双分子反应机理表明吸附的乙烯基表面扩散决定了1,3-丁二烯的形成速率。 Ag(111)表面上预先吸附的Cl导致物理吸附的氯乙烯在TDS中在150 K下解吸。此外,预吸附的Cl-Ag(111)增加了垂直附着所需的底物电子能量,因此减小了光化学离解截面。 HREELS表明,与没有预吸附Cl的情况相比,在Cl-Ag(111)表面上物理吸附的氯乙烯的分子平面与表面平面的平行度更高,并且氯乙烯“氢键”到Cl-Ag (111)。

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