Martinazzo Rocco, Tantardini Gian Franco
Department of Physical Chemistry and Electrochemistry and CIMAINA, University of Milan, Via Golgi 19, 20133 Milan, Italy.
J Chem Phys. 2006 Mar 28;124(12):124703. doi: 10.1063/1.2177655.
Following previous investigation of collision induced (CI) processes involving hydrogen atoms chemisorbed on graphite [R. Martinazzo and G. F. Tantardini, J. Chem. Phys. 124, 124702 (2006)], the case in which the target hydrogen atom is initially physisorbed on the surface is considered here. Several adsorbate-substrate initial states of the target H atom in the physisorption well are considered, and CI processes are studied for projectile energies up to 1 eV. Results show that (i) Eley-Rideal cross sections at low collision energies may be larger than those found in the H-chemisorbed case but they rapidly decrease as the collision energy increases; (ii) product hydrogen molecules are vibrationally very excited; (iii) collision induced desorption cross sections rapidly increase, reaching saturation values greater than 10 A2; (iv) trapping of the incident atoms is found to be as efficient as the Eley-Rideal reaction at low energies and remains sizable (3-4 A2) at high energies. The latter adsorbate-induced trapping results mainly in formation of metastable hot hydrogen atoms, i.e., atoms with an excess energy channeled in the motion parallel to the surface. These atoms might contribute in explaining hydrogen formation on graphite.
继先前对涉及化学吸附在石墨上的氢原子的碰撞诱导(CI)过程进行研究之后[R. Martinazzo和G. F. Tantardini,《化学物理杂志》124, 124702 (2006)],本文考虑目标氢原子最初物理吸附在表面的情况。考虑了目标H原子在物理吸附阱中的几种吸附质 - 衬底初始状态,并研究了入射能量高达1 eV时的CI过程。结果表明:(i)低碰撞能量下的埃利 - 里德截面可能大于化学吸附氢的情况,但随着碰撞能量增加迅速减小;(ii)产物氢分子振动激发程度很高;(iii)碰撞诱导解吸截面迅速增加,达到大于10 Ų的饱和值;(iv)发现入射原子的捕获在低能量下与埃利 - 里德反应一样有效,在高能量下仍相当可观(3 - 4 Ų)。后一种吸附质诱导的捕获主要导致亚稳态热氢原子的形成,即能量过剩的原子,其过剩能量沿平行于表面的运动方向传递。这些原子可能有助于解释石墨上氢的形成。