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Real-time detection of S(1D2) photofragments produced from the 1B2(1Σu+) state of CS2 by vacuum ultraviolet photoelectron imaging using 133 nm probe pulses

机译:使用133 nm探测脉冲通过真空紫外光电子成像实时检测由CS2的1B2(1Σu+)状态产生的S(1D2)碎片

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摘要

Ultrafast photodissociation dynamics from the 1B2(1Σu+) state of CS2 are studied by time-resolved photoelectron imaging using the fourth (4ω, 198 nm) and sixth (6ω, 133 nm) harmonics of a femtosecond Ti:sapphire laser. The 1B2 state of CS2 was prepared with the 4ω pulses, and subsequent dynamics were probed using the 6ω vacuum ultraviolet (VUV) pulses. The VUV pulses enabled real-time detection of S(1D2) photofragments, produced via CS2*(1B2(1Σu+)) → CS(X 1Σ+) + S(1D2). The photoionization signal of dissociating CS2*(1B2(1Σu+)) molecules starts to decrease at about 100 fs, while the S(1D2) fragments appear with a finite (ca. 400 fs) delay time after the pump pulse. Also discussed is the configuration interaction of the 1B2(1Σu+) state based on relative photoionization cross-sections to different cationic states.
机译:使用飞秒Ti:蓝宝石激光器的四次(4ω,198 nm)和第六次(6ω,133 nm)谐波通过时间分辨光电子成像研究了CS2的1B2(1Σu+)状态下的超快光解离动力学。用4ω脉冲准备CS2的1B2状态,并使用6ω真空紫外(VUV)脉冲探测随后的动力学。 VUV脉冲可以实时检测通过CS2 *(1B2(1Σu+))→CS(X1Σ+)+ S(1D2)产生的S(1D2)碎片。解离CS2 *(1B2(1Σu+))分子的光电离信号在大约100 fs处开始降低,而S(1D2)碎片在泵浦脉冲后出现有限的延迟时间(约400 fs)。还讨论了基于相对于不同阳离子状态的光电离截面的1B2(1Σu+)状态的构型相互作用。

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