TY - JOUR
T1 - Extending the potential of plasma-induced luminescence spectroscopy
AU - Clavé, Elise
AU - Gaft, Michael
AU - Motto-Ros, Vincent
AU - Fabre, Cécile
AU - Forni, Olivier
AU - Beyssac, Olivier
AU - Maurice, Sylvestre
AU - Wiens, Roger C.
AU - Bousquet, Bruno
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/3
Y1 - 2021/3
N2 - In the context of laser-induced breakdown spectroscopy (LIBS), plasma-induced luminescence (PIL) may be observed by tuning the temporal acquisition parameters (delay and gate). This approach provides useful information about minor elements in a sample. The broad range of excitation resulting from the laser-induced plasma enables the simultaneous observation of multiple luminescence emission bands. However, PIL results in damage to the sample due to laser ablation. Moreover, time resolution only enables the separation of emission signatures with different decay times; as a consequence, only luminescence signatures with long decay times may be observed separately from plasma emissions. In this study, we propose a new experimental approach to extend the potential of PIL spectroscopy. Our main idea is to generate a laser-induced plasma on a separate ablation target adjacent to the luminescent sample, which is hence protected from laser ablation. Moreover, the ablation target can be selected to ensure a stable plasma for PIL excitation. We also show that this setup enables the further study of the excitation mechanisms of PIL itself by varying the nature of the excitation source of PIL. Finally, we propose a new experimental setup that enables the study of the luminescence features of short decay times. We successfully tested this new approach on both artificial and natural crystals, showing luminescence emission bands of varying decay times.
AB - In the context of laser-induced breakdown spectroscopy (LIBS), plasma-induced luminescence (PIL) may be observed by tuning the temporal acquisition parameters (delay and gate). This approach provides useful information about minor elements in a sample. The broad range of excitation resulting from the laser-induced plasma enables the simultaneous observation of multiple luminescence emission bands. However, PIL results in damage to the sample due to laser ablation. Moreover, time resolution only enables the separation of emission signatures with different decay times; as a consequence, only luminescence signatures with long decay times may be observed separately from plasma emissions. In this study, we propose a new experimental approach to extend the potential of PIL spectroscopy. Our main idea is to generate a laser-induced plasma on a separate ablation target adjacent to the luminescent sample, which is hence protected from laser ablation. Moreover, the ablation target can be selected to ensure a stable plasma for PIL excitation. We also show that this setup enables the further study of the excitation mechanisms of PIL itself by varying the nature of the excitation source of PIL. Finally, we propose a new experimental setup that enables the study of the luminescence features of short decay times. We successfully tested this new approach on both artificial and natural crystals, showing luminescence emission bands of varying decay times.
UR - http://www.scopus.com/inward/record.url?scp=85100604577&partnerID=8YFLogxK
U2 - 10.1016/j.sab.2021.106111
DO - 10.1016/j.sab.2021.106111
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AN - SCOPUS:85100604577
SN - 0584-8547
VL - 177
JO - Spectrochimica Acta - Part B Atomic Spectroscopy
JF - Spectrochimica Acta - Part B Atomic Spectroscopy
M1 - 106111
ER -