School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, 28759 Bremen, Germany.
Phys Chem Chem Phys. 2010 Feb 14;12(6):1351-6. doi: 10.1039/b917967d. Epub 2009 Dec 7.
To investigate the vibrational dynamics in high-lying electronic states of molecules, a degenerate four-wave mixing (DFWM) process in combination with an initial pump pulse was employed. Applying this technique, the vibrational dynamics occurring in the high-lying E(0(2)g) ion-pair state of molecular bromine were investigated. The initial pump pulse is used to excite the B(3)Pi(0(+)u) state, from which the E(0(2)g) ion-pair state can be accessed in a subsequent DFWM process. By introducing an internal time delay in the DFWM process, the vibrational dynamics of the E(0(2)g) and B(3)Pi(0(+)u) states can be probed and analyzed. In most cases, the signals of the E(0(2)g) and B(3)(0(+)u) state dynamics are overlapping, which makes it difficult to identify the contributions of the respective states. To this end we show that it is possible to extract the contributions of the E(0(2)g) state by a spectral decomposition of the DFWM signal. These findings are circumstantiated by quantum dynamical calculations.
为了研究分子的高电子态中的振动动力学,采用了简并四波混频(DFWM)过程与初始泵浦脉冲相结合的方法。应用该技术,研究了溴分子的高电子态 E(0(2)g)离子对态中的振动动力学。初始泵浦脉冲用于激发 B(3)Pi(0(+)u)态,随后可以在后续的 DFWM 过程中进入 E(0(2)g)离子对态。通过在 DFWM 过程中引入内部时间延迟,可以探测和分析 E(0(2)g)和 B(3)Pi(0(+)u)态的振动动力学。在大多数情况下,E(0(2)g)和 B(3)(0(+)u)态动力学的信号重叠,这使得难以确定各自态的贡献。为此,我们表明通过对 DFWM 信号进行光谱分解可以提取 E(0(2)g)态的贡献。这些发现得到了量子动力学计算的证实。