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Formation of long-lived Rydberg states of H_2 at K impregnated surfaces

机译:K浸渍表面上H_2的长寿Rydberg态的形成

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摘要

The formation of Rydberg states of hydrogen molecules H_2~* at potassium promoted iron oxide surfaces at 900-1000 K is studied using pulsed laser fragmentation neutral time-of-flight measurements. Both neutral Rydberg states H_2~* and ions H_2~+ are observed to reach the detector, as well as electronically excited clusters of hydrogen of the Rydberg matter type. The Rydberg states H_2~* and ions H_2~+ are not formed by the laser the fluence is too low, and such particles are not observed from hydrogen molecules in the gas phase. They also carry an excess kinetic energy of < 1 eV due to laser fragmentation. This kinetic energy corresponds probably to Coulomb repulsion in the excited clusters with interionic distances of a few nanometers. The size of the signal of H_2~* varies strongly with the laser fluence at high fluences. The molecular Rydberg states are believed to be formed by transfer of electronic excitation energy from the Rydberg states of the alkali atoms K~*, which are formed at the sample surface.
机译:使用脉冲激光碎裂中性飞行时间测量研究了钾促进的氧化铁表面在900-1000 K时氢分子H_2〜*的Rydberg态的形成。观察到中性的里德堡态H_2〜*和离子H_2〜+都到达探测器,以及电子激发的里德堡物质类型的氢簇。激光未形成里德堡态H_2〜*和离子H_2〜+,注量太低,并且从气相中的氢分子中未观察到此类粒子。由于激光碎裂,它们还携带<1 eV的过剩动能。该动能可能对应于离子簇距离为几纳米的激发簇中的库仑排斥。 H_2〜*信号的大小在高注量时随激光注量而变化很大。人们认为分子里德堡态是由电子激发能从碱原子K〜*的里德堡态转移而形成的,而碱原子K〜*在样品表面形成。

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