Department of Chemistry and Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720, USA.
J Chem Phys. 2012 Jun 7;136(21):214303. doi: 10.1063/1.4722924.
Neutral superexcited states in molecular oxygen converging to the O(2)(+) c (4)Σ(u)(-) ion state are excited and probed with femtosecond time-resolved photoelectron spectroscopy to investigate predissociation and autoionization relaxation channels as the superexcited states decay. The c (4)Σ(u)(-) 4sσ(g) v=0, c (4)Σ(u)(-) 4sσ(g) v=1, and c (4)Σ(u)(-) 3dσ(g) v=1 superexcited states are prepared with pulsed high-harmonic radiation centered at 23.10 eV. A time-delayed 805 nm laser pulse is used to probe the excited molecular states and neutral atomic fragments by ionization; the ejected photoelectrons from these states are spectrally resolved with a velocity map imaging spectrometer. Three excited neutral O* atom products are identified in the photoelectron spectrum as 4d(1) (3)D(J)°, 4p(1) (5)P(J)° and 3d(1) (3)D(J)° fragments. Additionally, several features in the photoelectron spectrum are assigned to photoionization of the transiently populated superexcited states. Using principles of the ion core dissociation model, the atomic fragments measured are correlated with the molecular superexcited states from which they originate. The 4d(1) (3)D(J)° fragment is observed to be formed on a timescale of 65 ± 5 fs and is likely a photoproduct of the 4sσ(g) v = 1 state. The 4p(1) (5)P(J)° fragment is formed on a timescale of 427 ± 75 fs and correlated with the neutral predissociation of the 4sσ(g) v = 0 state. The timescales represent the sum of predissociation and autoionization decay rates for the respective superexcited state. The production of the 3d(1) (3)D(J)° fragment is not unambiguously resolved in time due to an overlapping decay of a v = 1 superexcited state photoelectron signal. The observed 65 fs timescale is in good agreement with previous experiments and theory on the predissociation lifetimes of the v = 1 ion state, suggesting that predissociation may dominate the decay dynamics from the v = 1 superexcited states. An unidentified molecular state is inferred by the detection of a long-lived depletion signal (reduction in autoionization) associated with the B (2)Σ(g)(-) ion state that persists up to time delays of 105 ps.
中性超激发态分子氧向 O(2)(+) c (4)Σ(u)(-) 离子态的汇聚通过飞秒时间分辨光电子能谱进行激发和探测,以研究超激发态衰变时的预解离和自电离弛豫通道。c (4)Σ(u)(-) 4sσ(g) v=0、c (4)Σ(u)(-) 4sσ(g) v=1 和 c (4)Σ(u)(-) 3dσ(g) v=1 超激发态是用中心波长为 23.10 eV 的脉冲高次谐波辐射制备的。用延迟的 805nm 激光脉冲通过离化来探测激发的分子态和中性原子碎片;这些态中逐出的光电子通过速度映射成像谱仪进行光谱分辨。在光电子谱中识别出三种激发的中性 O*原子产物为 4d(1) (3)D(J)°、4p(1) (5)P(J)°和 3d(1) (3)D(J)°碎片。此外,光电子谱中的几个特征被分配给瞬态超激发态的光致电离。利用离子核解离模型的原理,测量的原子碎片与它们起源的分子超激发态相关联。4d(1) (3)D(J)°碎片的形成时间为 65±5fs,可能是 4sσ(g) v = 1 态的光产物。4p(1) (5)P(J)°碎片的形成时间为 427±75fs,与 4sσ(g) v = 0 态的中性预解离相关联。这些时间尺度代表了各自超激发态的预解离和自电离衰变速率的总和。由于 v = 1 超激发态光电子信号的重叠衰减,3d(1) (3)D(J)°碎片的产生在时间上无法明确分辨。观察到的 65fs 时间尺度与先前关于 v = 1 离子态预解离寿命的实验和理论非常吻合,表明预解离可能主导 v = 1 超激发态的衰变动力学。与 B (2)Σ(g)(-) 离子态相关联的长寿命耗尽信号(自电离减少)的检测推断出一个未识别的分子态,该信号持续到 105ps 的延迟时间。