Abstract

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 since 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.

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