Crystal-field analysis, upconversion, and excited-state dynamics for(U4+,U3+):Ba2YCl7single crystals

2003 ◽  
Vol 67 (19) ◽  
Author(s):  
Mirosław Karbowiak ◽  
Agnieszka Mech ◽  
Janusz Drożdżyński ◽  
Norman M. Edelstein
Open Physics ◽  
2005 ◽  
Vol 3 (4) ◽  
Author(s):  
Mikhail Brik ◽  
Nicolae Avram ◽  
Calin Avram

AbstractThe exchange charge model of crystal field theory has been used to analyze the ground and excited state absorption of tetrahedrally coordinated Cr4+ ion in lithium aluminum oxide LiAlO2 (γ-phase) and lithium dioxogallate LiGaO2. The parameters of the crystal field acting on the Cr4+ ion are calculated from the crystal structure data, taking into account the crystal lattice ions located at distances up to 12.744 Å in LiGaO2 and 13. 180 Å in LiAlO2. The obtained energy level schemes were compared with experimental ground and excited state absorption spectra and literature data on the application of other crystal field models (the angular overlap model and Racah theory) to the considered crystals; a good agreement with experimental data is demonstrated.


Small ◽  
2011 ◽  
Vol 7 (21) ◽  
pp. 3046-3056 ◽  
Author(s):  
Wenqin Luo ◽  
Chengyu Fu ◽  
Renfu Li ◽  
Yongsheng Liu ◽  
Haomiao Zhu ◽  
...  

2007 ◽  
Vol 432 (1-2) ◽  
pp. 61-68 ◽  
Author(s):  
M.G. Brik ◽  
N.M. Avram ◽  
C.N. Avram ◽  
C. Rudowicz ◽  
Y.Y. Yeung ◽  
...  

2019 ◽  
Author(s):  
Matthew M. Brister ◽  
Carlos Crespo-Hernández

<p></p><p> Damage to RNA from ultraviolet radiation induce chemical modifications to the nucleobases. Unraveling the excited states involved in these reactions is essential, but investigations aimed at understanding the electronic-energy relaxation pathways of the RNA nucleotide uridine 5’-monophosphate (UMP) have not received enough attention. In this Letter, the excited-state dynamics of UMP is investigated in aqueous solution. Excitation at 267 nm results in a trifurcation event that leads to the simultaneous population of the vibrationally-excited ground state, a longlived <sup>1</sup>n<sub>O</sub>π* state, and a receiver triplet state within 200 fs. The receiver state internally convert to the long-lived <sup>3</sup>ππ* state in an ultrafast time scale. The results elucidate the electronic relaxation pathways and clarify earlier transient absorption experiments performed for uracil derivatives in solution. This mechanistic information is important because long-lived nπ* and ππ* excited states of both singlet and triplet multiplicities are thought to lead to the formation of harmful photoproducts.</p><p></p>


2019 ◽  
Author(s):  
Gergely Samu ◽  
R.A. Scheidt ◽  
A. Balog ◽  
C. Janáky ◽  
P.V. Kamat

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