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首页> 外文期刊>The Journal of Chemical Physics >Methane dissociative chemisorption and detailed balance on Pt(111): Dynamical constraints and the modest influence of tunneling
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Methane dissociative chemisorption and detailed balance on Pt(111): Dynamical constraints and the modest influence of tunneling

机译:甲烷解离化学吸附和Pt(111)的详细平衡:动力学约束和隧穿的适度影响

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A dynamically biased (d-) precursor mediated microcanonical trapping (PMMT) model of the activated dissociative chemisorption of methane on Pt(111) is applied to a wide range of dissociative sticking experiments, and, by detailed balance, to the methane product state distributions from the thermal associative desorption of adsorbed hydrogen with coadsorbed methyl radicals. Tunneling pathways were incorporated into the d-PMMT model to better replicate the translational energy distribution of the desorbing methane product from the laser induced thermal reaction of coadsorbed hydrogen and methyl radicals occurring near T_s = 395 K. Although tunneling is predicted to be inconsequential to the thermal dissociative chemisorption of CH_4 on Pt(111) at the high temperatures of catalytic interest, once the temperature drops to 395 K the tunneling fraction of the reactive thermal flux reaches 15%, and as temperatures drop below 275 K the tunneling fraction exceeds 50%. The d-PMMT model parameters of {E_0 = 58.9 kJ/mol, s = 2, η_v = 0.40} describe the apparent threshold energy for CH_4/Pt(111) dissociative chemisorption, the number of surface oscillators involved in the precursor complex, and the efficacy of molecular vibrational energy to promote reaction, relative to translational energy directed along the surface normal. Molecular translations parallel to the surface and rotations are treated as spectator degrees of freedom. Transition state vibrational frequencies are derived from generalized gradient approximation-density functional theory electronic structure calculations. The d-PMMT model replicates the diverse range of experimental data available with good fidelity, including some new effusive molecular beam and ambient gas dissociative sticking measurements. Nevertheless, there are some indications that closer agreement between theory and experiments could be achieved if a surface efficacy less than one was introduced into the modeling as an additional dynamical constraint.
机译:活化的Pt(111)上甲烷的活化解离化学吸附的动态偏置(d-)前体介导的微规范捕集(PMMT)模型适用于广泛的解离黏附实验,并通过详细的平衡应用于甲烷产物的状态分布由吸附的氢与共吸附的甲基的热缔合解吸引起。将隧穿路径纳入d-PMMT模型中,以更好地复制T_s = 395 K附近发生的共吸附氢和甲基自由基的激光诱导热反应的解吸甲烷产物的平移能量分布。在催化作用下的高温下,CH_4在Pt(111)上的热解离化学吸附,一旦温度降至395 K,反应性热通量的隧穿分数达到15%,并且当温度降至275 K以下时,隧穿分数超过50% 。 d-PMMT模型参数{E_0 = 58.9 kJ / mol,s = 2,η_v= 0.40}描述了CH_4 / Pt(111)解离化学吸附的表观阈值能量,前体络合物中涉及的表面振荡器的数量,以及相对于沿表面法线定向的平移能,分子振动能促进反应的功效。平行于表面和旋转的分子平移被视为观众的自由度。过渡态振动频率是从广义梯度近似密度泛函理论电子结构计算得出的。 d-PMMT模型以高保真度复制了各种可用的实验数据,包括一些新的喷射性分子束和环境气体解离粘附测量。然而,有迹象表明,如果将表面功效小于1的表面功效作为附加的动力学约束引入模型中,则可以在理论和实验之间达成更紧密的共识。

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