Seijo Luis, Barandiarán Zoila
Departamento de Química, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Instituto Universitario de Ciencia de Materiales Nicolás Cabrera, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
J Chem Phys. 2014 Dec 7;141(21):214706. doi: 10.1063/1.4902384.
The existence of intervalence charge transfer (IVCT) luminescence is reported. It is shown that the so called anomalous luminescence of Ce-doped elpasolite Cs2LiLuCl6, which is characterized mainly by a very large Stokes shift and a very large band width, corresponds to an IVCT emission that takes place in Ce(3+)-Ce(4+) pairs, from the 5de(g) orbital of Ce(3+) to 4f orbitals of Ce(4+). Its Stokes shift is the sum of the large reorganization energies of the Ce(4+) and Ce(3+) centers formed after the fixed-nuclei electron transfer and it is equal to the energy of the IVCT absorption commonly found in mixed-valence compounds, which is predicted to exist in this material and to be slightly larger than 10,000 cm(-1). The large band width is the consequence of the large offset between the minima of the Ce(3+)-Ce(4+) and Ce(4+)-Ce(3+) pairs along the electron transfer reaction coordinate. This offset is approximately 2√3 times the difference of Ce-Cl equilibrium distances in the Ce(3+) and Ce(4+) centers. It is shown that the energies of the peaks and the widths of IVCT absorption and emission bands can be calculated ab initio with reasonable accuracy from diabatic energy surfaces of the ground and excited states and that these can be obtained, in turn, from independent calculations on the donor and acceptor active centers. We obtained the energies of the Ce(3+) and Ce(4+) active centers of Ce-doped Cs2LiLuCl6 by means of state-of-the-art wave-function-theory spin-orbit coupling relativistic calculations on the donor cluster (CeCl6Li6Cs8)(11+) and the acceptor cluster (CeCl6Li6Cs8)(12+) embedded in a quantum mechanical embedding potential of the host. The calculations provide interpretations of unexplained experimental observations as due to higher energy IVCT absorptions, and allow to reinterpret others. The existence of another IVCT emission of lower energy, at around 14,000-16,000 cm(-1) less than the 5dt(2g) emission, is also predicted.
报道了价间电荷转移(IVCT)发光的存在。结果表明,铈掺杂的铯锂镥氯石Cs2LiLuCl6中所谓的反常发光,其主要特征是具有非常大的斯托克斯位移和非常大的带宽,对应于Ce(3+)-Ce(4+)对中发生的IVCT发射,即从Ce(3+)的5de(g)轨道到Ce(4+)的4f轨道。其斯托克斯位移是固定核电子转移后形成的Ce(4+)和Ce(3+)中心的大重组能之和,并且等于混合价化合物中常见的IVCT吸收能量,预计该材料中存在这种吸收且略大于10,000 cm(-1)。大带宽是Ce(3+)-Ce(4+)和Ce(4+)-Ce(3+)对沿电子转移反应坐标的最小值之间存在大偏移的结果。该偏移约为Ce(3+)和Ce(4+)中心中Ce-Cl平衡距离差的2√3倍。结果表明,IVCT吸收和发射带的峰能量和宽度可以从基态和激发态的非绝热能量表面从头算得到合理的精度,而这些能量表面又可以通过对供体和受体活性中心的独立计算获得。我们通过对嵌入主体量子力学嵌入势中的供体簇(CeCl6Li6Cs8)(11+)和受体簇(CeCl6Li6Cs8)(12+)进行最先进的波函数理论自旋轨道耦合相对论计算,得到了铈掺杂Cs2LiLuCl6中Ce(3+)和Ce(4+)活性中心的能量。这些计算对未解释的实验观测结果给出了解释,认为是由于更高能量的IVCT吸收,并允许对其他结果进行重新解释。还预测存在另一种能量较低的IVCT发射,比5dt(2g)发射低约14,000 - 16,000 cm(-1)。