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H2S ultrafast dissociation probed by energy-selected resonant Auger electron-ion coincidence measurements

机译:通过能量选择共振俄歇电子离子重合度测量探测H2S超快解离

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We have studied the ultrafast dissociation of the H2S molecule upon S 2p(3/2)-> 6a(1) inner-shell excitation by combining high-resolution resonant Auger spectroscopy and energy-selected Auger electron-ion coincidence measurements. Auger final states have been correlated to the different fragmentation pathways (S+, HS+, and H2S+ ions). As an original result, we evidence a three-stEP 1mechanism to describe the resonant production of S+: the Auger recombination in the HS* fragment is followed for the A (3)Pi and c (1)Pi states by the S++H fragmentation mechanism. (c) 2007 American Institute of Physics.
机译:我们已经通过结合高分辨率共振俄歇光谱和能量选择的俄歇电子离子符合测量,研究了在S 2p(3/2)-> 6a(1)内壳激发下H2S分子的超快解离。俄歇的最终状态已与不同的裂解途径(S +,HS +和H2S +离子)相关。作为原始结果,我们证明了三步法1机制来描述S +的共振产生:S ++ H遵循A *(3)Pi和c(1)Pi状态在HS *片段中进行俄歇重组。碎片化机制。 (c)2007年美国物理研究所。

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