Resonant Auger spectra of O-2 clusters excited at the O1s edge are reported. After excitation to the repulsive 1s(-1)3 sigma* state, the resulting resonant Auger spectrum displays features that remain constant in kinetic energy as the photon energy is detuned. The shift between known atomic fragment features and these features is consistent with that observed for atoms and clusters in singly charged states in direct photoemission. These findings are strong evidence for the existence of molecular ultrafast dissociation processes within the clusters or on their surface
We have studied the ultrafast dissociation of the H2S molecule upon S 2p(3/2)-> 6a(1) inner-shell ex...
Resonance K auger spectra of molecular oxygen are presented at photon energies corresponding to 1σ→1...
Resonant Auger decay of core-excited molecules during ultrafast dissociation leads to a Doppler shif...
Resonant Auger spectra of O2 clusters excited at the O1s edge are reported. After excitation to the ...
We present direct evidence for ultra-fast dissociation of molecular water in connection photo-excita...
We present evidence for ultra-fast dissociation of molecular ammonia when photo-excited to the Nls -...
We address the influence of clustering on the ultra-fast dissociation of bromomethane. Valence and c...
The below-threshold region in core-excited O2 is very complex, consisting of a multitude of exchange...
International audienceA Doppler-type shift in the kinetic energy of atomic Auger electrons emitted a...
Resonance K auger spectra of molecular oxygen are presented at photon energies corresponding to 1sim...
International audienceWhen an electron is resonantly excited from a core orbital to a Rydberg one in...
Following core excitation in an isolated molecule, ultrafast dissociation of one particular chemical...
Abstract When an electron is resonantly excited from a core orbital to a Rydberg one in a molecule,...
International audienceWe have studied the ultrafast dissociation of the H2S molecule upon S 2p3/26a1...
We address the influence of clustering on the ultra-fast dissociation of bromomethane. Valence and c...
We have studied the ultrafast dissociation of the H2S molecule upon S 2p(3/2)-> 6a(1) inner-shell ex...
Resonance K auger spectra of molecular oxygen are presented at photon energies corresponding to 1σ→1...
Resonant Auger decay of core-excited molecules during ultrafast dissociation leads to a Doppler shif...
Resonant Auger spectra of O2 clusters excited at the O1s edge are reported. After excitation to the ...
We present direct evidence for ultra-fast dissociation of molecular water in connection photo-excita...
We present evidence for ultra-fast dissociation of molecular ammonia when photo-excited to the Nls -...
We address the influence of clustering on the ultra-fast dissociation of bromomethane. Valence and c...
The below-threshold region in core-excited O2 is very complex, consisting of a multitude of exchange...
International audienceA Doppler-type shift in the kinetic energy of atomic Auger electrons emitted a...
Resonance K auger spectra of molecular oxygen are presented at photon energies corresponding to 1sim...
International audienceWhen an electron is resonantly excited from a core orbital to a Rydberg one in...
Following core excitation in an isolated molecule, ultrafast dissociation of one particular chemical...
Abstract When an electron is resonantly excited from a core orbital to a Rydberg one in a molecule,...
International audienceWe have studied the ultrafast dissociation of the H2S molecule upon S 2p3/26a1...
We address the influence of clustering on the ultra-fast dissociation of bromomethane. Valence and c...
We have studied the ultrafast dissociation of the H2S molecule upon S 2p(3/2)-> 6a(1) inner-shell ex...
Resonance K auger spectra of molecular oxygen are presented at photon energies corresponding to 1σ→1...
Resonant Auger decay of core-excited molecules during ultrafast dissociation leads to a Doppler shif...