Lehtonen Olli, Sundholm Dage
Department of Engineering Physics and Mathematics, Helsinki University of Technology, PO Box 2200, FIN-02015, HUT, Espoo, Finland.
Phys Chem Chem Phys. 2006 Sep 28;8(36):4228-32. doi: 10.1039/b606643g. Epub 2006 Aug 10.
Time-dependent density functional theory (TDDFT) calculations show that silicon nanoclusters (Si-NC) capped by linear silane groups have large oscillator strengths of the same magnitude as reported in recent experimental studies. We propose a mechanism where linear silanes attached to the Si-NC surface affect the optical properties enhancing the oscillator strengths and thereby accounting for the bright luminescence observed in the blue region of the visible spectrum. The anisotropic emission seen experimentally can also be explained by the presence of the silane groups on the cluster surface. The excitation energies are found to be only slightly affected by the silanes, whereas the oscillator strengths increase with the length of the silane chain and are significantly larger than obtained for unsubstituted Si-NCs. In TDDFT studies of Si-NC dimers interconnected by a linear silane bridge, we obtained large oscillator strengths indicating that such structures could be useful light sources for optical devices.
含时密度泛函理论(TDDFT)计算表明,由线性硅烷基封端的硅纳米团簇(Si-NC)具有与近期实验研究报道相同量级的大振子强度。我们提出了一种机制,即附着在Si-NC表面的线性硅烷会影响光学性质,增强振子强度,从而解释了在可见光谱蓝色区域观察到的明亮发光现象。实验中观察到的各向异性发射也可以通过团簇表面存在硅烷基来解释。发现激发能仅受到硅烷的轻微影响,而振子强度随着硅烷链长度的增加而增大,并且明显大于未取代的Si-NC所获得的振子强度。在通过线性硅烷桥互连的Si-NC二聚体的TDDFT研究中,我们获得了大振子强度,表明这种结构可能是光学器件的有用光源。