多光子电离/分离分子硫 S2 在紫外线区域
Zhongfa Sun1, Zahid Farooq2,3, Zhichao Chen4
1Anhui Province Key Laboratory for Control and Applications of Optoelectronic Information Materials, Department of Physics, Anhui Normal University, Wuhu, Anhui 241002, China.
The journal of physical chemistry. A
|May 9, 2024
概括
研究了硫分子 (S2) 的多光子电离和解离. 与激发的硫原子的解离占主导地位,超过自电离,揭示了与O2相比独特的光动力学.
科学领域:
- 物理化学 物理化学
- 分子光谱学 分子光谱学
- 摄影化学的使用.
背景情况:
- 分子硫 (S2) 表现出复杂的光物理行为.
- 了解S2动态对于大气和天体物理化学至关重要.
研究的目的:
- 阐明S2在紫外线范围 (205-300 nm) 中的多光子电离/解离动态.
- 在S2中研究过度兴奋状态的衰变路径.
- 为了比较S2光动力学与电子相似的O2.
主要方法:
- 速度图像离子成像 (VMI) 技术用于单色实验.
- 脉冲放电被用来产生分子硫 (S).
- 光解离是由紫外线辐射诱导的.
主要成果:
- 超兴奋状态通过B3Σu-和Rydberg状态访问.
- 对电子激发的 S 原子的解离在 λ < 288 nm 的自离离子化上占主导地位.
- 自动化在S (D) 和S (S) 检测波长在288 nm左右是有效的.
- 振动激发的S2+ (X2+ (v11)) 已被确定.
结论:
- 这项研究揭示了S2的独特光动力学,与O2有显著差异.
- 对兴奋的S原子的解离是超兴奋的S2的主要衰变通道.
- 在S2+中的振动激发会影响其解离路径.
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