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Vacuum ultraviolet spectroscopy of the Cl2 molecule trapped in pure neon, pure argon, or mixed neon–argon matrices

Peter Gürtler, H. Kunz, JACQUES LE CALVE

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Abstract

Synchrotron radiation excitation and emission spectra with lifetime measurements are reported for the first time in the VUV region for systems consisting of Cl2 molecules trapped in a neon matrix, an argon matrix, and mixed Ar/Ne matrices. In pure neon, the emission spectrum of the D′→A′ ‘‘laser’’ transition at 4.7 eV of the Cl2 molecule is vibrationally well resolved and constitutes an interesting example of UV spectroscopy of a matrix ‘‘isolated’’ molecule. In pure argon or mixed Ar/Ne matrices, new broad emissions at 4.1, 3.8, and 3.5 eV are clearly identified, which result from the specific interaction between Cl*2 and Ar and are attributed to different charge–transfer states of the ArCl+Cl− entity. The Ar concentration dependence and the time-gated spectra are shown to be especially useful in interpreting the large differences observed between the pure neon and the pure argon matrix case.

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What this paper is about

Synchrotron radiation excitation and emission spectra with lifetime measurements are reported for the first time in the VUV region for systems consisting of Cl2 molecules trapped in a neon matrix, an argon matrix, and mixed Ar/Ne matrices. In pure neon, the emission spectrum of the D′→A′ ‘‘laser’’ transition at 4.7 eV of the Cl2 molecule is vibrationally well resolved and constitutes an interesting example of UV spectroscopy of a matrix ‘‘isolated’’ molecule. In pure argon or mixed Ar/Ne matrices, new broad emissions at 4.1, 3.8, and 3.5 eV are clearly identified, which result from the specific interaction between Cl*2 and Ar and are attributed to different charge–transfer states of the ArCl+Cl− entity. The Ar concentration dependence and the time-gated spectra are shown to be especially useful in interpreting the large differences observed between the pure neon and the pure argon matrix case.

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Available abstract

Synchrotron radiation excitation and emission spectra with lifetime measurements are reported for the first time in the VUV region for systems consisting of Cl2 molecules trapped in a neon matrix, an argon matrix, and mixed Ar/Ne matrices. In pure neon, the emission spectrum of the D′→A′ ‘‘laser’’ transition at 4.7 eV of the Cl2 molecule is vibrationally well resolved and constitutes an interesting example of UV spectroscopy of a matrix ‘‘isolated’’ molecule. In pure argon or mixed Ar/Ne matrices, new broad emissions at 4.1, 3.8, and 3.5 eV are clearly identified, which result from the specific interaction between Cl*2 and Ar and are attributed to different charge–transfer states of the ArCl+Cl− entity. The Ar concentration dependence and the time-gated spectra are shown to be especially useful in interpreting the large differences observed between the pure neon and the pure argon matrix case.

Key concepts: Neon, Argon, Atomic physics, Spectroscopy, Molecule, Matrix isolation, Emission spectrum, Matrix (chemical analysis)

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