Institute of Physics and Chemistry, University of Southern Denmark, Odense DK-5230, Denmark.
J Chem Phys. 2009 Dec 28;131(24):244707. doi: 10.1063/1.3274655.
Direct D atom desorption, as well as associative desorption of D(2) molecules are observed in thermal desorption from D atoms chemisorbed on a C(0001) surface by combining laser induced T-jumps with resonance enhanced multiphoton ionization detection. Bleaching curves suggest that different classes of chemisorbed D atom clusters are present on the initial surface. The energy resolved atomic desorption flux, obtained via time of flight techniques, compares favorably (via detailed balance) with theoretical calculations of atomic sticking. Density functional theory calculations of chemical processes (atomic desorption, atomic diffusion/cluster annealing, and associative desorption) on an extensive set of four atom H(D) clusters chemisorbed on C(0001) provide a good interpretation of the experiments. State and energy resolved D(2) desorption fluxes are compared with previous state averaged results. In combination with density functional theory calculations these measurements reveal a substantial energy loss (>1 eV) to the surface in the associative desorption.
通过将激光诱导的 T-jump 与共振增强多光子电离检测相结合,观察到 D 原子在 C(0001)表面化学吸附的 D 原子的直接 D 原子解吸,以及 D(2)分子的缔合解吸。漂白曲线表明,初始表面上存在不同类别的化学吸附 D 原子簇。通过飞行时间技术获得的能量分辨原子解吸通量,与原子附着的理论计算(通过详细平衡)相比非常吻合。在广泛的四个原子 H(D)簇化学吸附在 C(0001)上的化学过程(原子解吸、原子扩散/簇退火和缔合解吸)的密度泛函理论计算,为实验提供了很好的解释。状态和能量分辨的 D(2)解吸通量与之前的状态平均结果进行了比较。这些测量结果与密度泛函理论计算相结合,揭示了缔合解吸过程中表面的能量损失(>1 eV)相当大。