Er-Related Emission In Impurities (Nitrogen, Oxygen) Implanted Al0.7Ga0.3As

1997 ◽  
Vol 484 ◽  
Author(s):  
S. Uekusa ◽  
M. Wakutani ◽  
M. Saito ◽  
M. Kumagai

AbstractErbium (Er) was co-implanted with ( i ) nitrogen (N), ( ii) oxygen (0) and (iii) N and 0 into Al0.7Ga0.3As substrates. Compared with the Al0.7Ga0.3As:Er sample, the 20 K Er3+ -related 1.54 μm integrated photoluminescence (PL) intensity from the Al0 7Ga0.3As:Er,N and Al0.7Ga0.3As:Er,N,O samples were enhanced approximately fifteen and ten times more, respectively. Thermal quenching of Er3+-related emission from Al0.7Ga0.3As:Er,N,O was smaller than that of Er3+-related emission from Al0.7.Ga0.3As-Er,N The 20 K Er3+-related 0.98 μm PL which was radiated by transition from the second excited state (4I1/2) to the ground state (4I1/2) was observed. The 0.98 μm PL intensity from Al0.7Ga0.3As:Er,N,O generally decreased with increasing 0 dosage from 1 × 1013 cm−2 to 1 × 1015 cm−2. These results suggest the formation of different complexes composed of Er and the impurities (N,O). This leads to the generation of complex related traps in the band-gap of Al0.7Ga0.3As as a result of the co-implantation of the impurities. It was found that the trap level of the Er-N complex center lay between 2.05 eV and 1.26 eV, and that of the Er-N-O complex center lay between 1.26 eV and 0.82 eV.

2002 ◽  
Vol 744 ◽  
Author(s):  
Shin-ichiro Uekusa ◽  
Isao Tanaka ◽  
Tomoyuki. Arai

ABSTRACTErbium (Er) ions were co-implanted with ytterbium (Yb) into Al0.70Ga0.30As substrates and we realized an increase in the intensity of Er intra-4f-shell luminescence. The photoluminescence (PL) intensity of Er-related dominant peak (1538.2nm) was enhanced by co-implanted Yb. The thermal quenching was improved. PL intensity of Yb-related emission was decreased. We studied the transfer energy and the optical sensitization of Yb ions co-implanted with Er ions in Al0.70Ga0.30As. Energy transfers from 2F5/2 (the first excited state) → 2F7/2 (the ground state) of Yb3+ to 4I13/2 (the first excited state) → 4I15/2 (the ground state) of Er3+ were observed by PL excitation (PLE) and selectively excited PL (SPL).


Author(s):  
Ben O. Spurlock ◽  
Milton J. Cormier

The phenomenon of bioluminescence has fascinated layman and scientist alike for many centuries. During the eighteenth and nineteenth centuries a number of observations were reported on the physiology of bioluminescence in Renilla, the common sea pansy. More recently biochemists have directed their attention to the molecular basis of luminosity in this colonial form. These studies have centered primarily on defining the chemical basis for bioluminescence and its control. It is now established that bioluminescence in Renilla arises due to the luciferase-catalyzed oxidation of luciferin. This results in the creation of a product (oxyluciferin) in an electronic excited state. The transition of oxyluciferin from its excited state to the ground state leads to light emission.


1996 ◽  
Vol 6 (9) ◽  
pp. 1167-1180 ◽  
Author(s):  
A. Gicquel ◽  
M. Chenevier ◽  
Y. Breton ◽  
M. Petiau ◽  
J. P. Booth ◽  
...  

2020 ◽  
Author(s):  
Tomislav Rovis ◽  
Benjamin D. Ravetz ◽  
Nicholas E. S. Tay ◽  
Candice Joe ◽  
Melda Sezen-Edmonds ◽  
...  

We describe a new family of catalysts that undergo direct ground state singlet to excited state triplet excitation with IR light, leading to photoredox catalysis without the energy waste associated with intersystem crossing. The finding allows a mole scale reaction in batch using infrared irradiation.


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>


2021 ◽  
Vol 23 (14) ◽  
pp. 8525-8540
Author(s):  
Mudong Feng ◽  
Michael K. Gilson

Ground-state and excited-state molecular dynamics simulations shed light on the rotation mechanism of small, light-driven molecular motors and predict motor performance. How fast can they rotate; how much torque and power can they generate?


1990 ◽  
Vol 26 (5) ◽  
pp. 320 ◽  
Author(s):  
M. Monerie ◽  
T. Georges ◽  
P.L. Francois ◽  
J.Y. Allain ◽  
D. Neveux

2017 ◽  
Vol 474 (16) ◽  
pp. 2713-2731 ◽  
Author(s):  
Athinoula L. Petrou ◽  
Athina Terzidaki

From kinetic data (k, T) we calculated the thermodynamic parameters for various processes (nucleation, elongation, fibrillization, etc.) of proteinaceous diseases that are related to the β-amyloid protein (Alzheimer's), to tau protein (Alzheimer's, Pick's), to α-synuclein (Parkinson's), prion, amylin (type II diabetes), and to α-crystallin (cataract). Our calculations led to ΔG≠ values that vary in the range 92.8–127 kJ mol−1 at 310 K. A value of ∼10–30 kJ mol−1 is the activation energy for the diffusion of reactants, depending on the reaction and the medium. The energy needed for the excitation of O2 from the ground to the first excited state (1Δg, singlet oxygen) is equal to 92 kJ mol−1. So, the ΔG≠ is equal to the energy needed for the excitation of ground state oxygen to the singlet oxygen (1Δg first excited) state. The similarity of the ΔG≠ values is an indication that a common mechanism in the above disorders may be taking place. We attribute this common mechanism to the (same) role of the oxidative stress and specifically of singlet oxygen, (1Δg), to the above-mentioned processes: excitation of ground state oxygen to the singlet oxygen, 1Δg, state (92 kJ mol−1), and reaction of the empty π* orbital with high electron density regions of biomolecules (∼10–30 kJ mol−1 for their diffusion). The ΔG≠ for cases of heat-induced cell killing (cancer) lie also in the above range at 310 K. The present paper is a review and meta-analysis of literature data referring to neurodegenerative and other disorders.


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