Department of Photo-Molecular Science, Institute for Molecular Science, Okazaki 444-8585 Japan.
J Chem Phys. 2011 Jul 21;135(3):034704. doi: 10.1063/1.3610530.
The local electronic structures of crystalline and amorphous films of zinc phthalocyanine (ZnPc) and metal-free phthalocyanine (H(2)Pc) have been studied by soft x-ray emission spectroscopy (XES). We found a clear crystalline structure dependence of the elastic-peak shape in the resonant XES spectra. The elastic peaks of both ZnPc and H(2)Pc are found to show an asymmetric shape due to resonant inelastic x-ray scattering (RIXS) at the nitrogen sites for the α-crystalline films, but not for the amorphous films. The observed RIXS feature is ascribed to the charge transfer excitation due to the Raman-active intermolecular interaction, which dominates the excited-electron dynamics in α-crystalline phthalocyanine films.
通过软 X 射线发射光谱(XES)研究了晶体和非晶态锌酞菁(ZnPc)和无金属酞菁(H(2)Pc)薄膜的局域电子结构。我们发现共振 XES 光谱中的弹性峰形状具有明显的晶体结构依赖性。由于α-晶态薄膜中氮位的共振非弹性 X 射线散射(RIXS),ZnPc 和 H(2)Pc 的弹性峰均呈现不对称形状,但非晶态薄膜则不然。观察到的 RIXS 特征归因于电荷转移激发,这是由于拉曼活性分子间相互作用引起的,它主导了α-晶态酞菁薄膜中激发电子的动力学。