Molecular beam studies of weak interactions for open‐shell systems: The ground and lowest excited states of rare gas oxides

1988 ◽  
Vol 89 (10) ◽  
pp. 6157-6164 ◽  
Author(s):  
Vincenzo Aquilanti ◽  
Roberto Candori ◽  
Fernando Pirani
Keyword(s):  
Excited States ◽  
Molecular Beam ◽  
Weak Interactions ◽  
Open Shell ◽  
Rare Gas

Molecular beam studies of weak interactions of open-shell atoms: the ground and lowest excited states of rare-gas chlorides

1993 ◽  
Vol 97 (10) ◽  
pp. 2063-2071 ◽  
Author(s):  
Vincenzo Aquilanti ◽  
David Cappelletti ◽  
Vincent Lorent ◽  
Emilio Luzzatti ◽  
Fernando Pirani
Keyword(s):  
Excited States ◽  
Molecular Beam ◽  
Weak Interactions ◽  
Open Shell ◽  
Rare Gas

Molecular beam studies of weak interactions for open‐shell systems: The ground and lowest excited states of ArF, KrF, and XeF

1988 ◽  
Vol 89 (10) ◽  
pp. 6165-6175 ◽  
Author(s):  
Vincenzo Aquilanti ◽  
Emilio Luzzatti ◽  
Fernando Pirani ◽  
Gian Gualberto Volpi
Keyword(s):  
Excited States ◽  
Molecular Beam ◽  
Weak Interactions ◽  
Open Shell

scholarly journals Influence of TOPO and TOPO-CdSe/ZnS Quantum Dots on Luminescence Photodynamics of InP/InAsP/InPHeterostructure Nanowires

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 640
Author(s):  
Artem I. Khrebtov ◽  
Vladimir V. Danilov ◽  
Anastasia S. Kulagina ◽  
Rodion R. Reznik ◽  
Ivan D. Skurlov ◽  
...  
Keyword(s):  
Quantum Dots ◽  
Excited States ◽  
Molecular Beam ◽  
Surface Passivation ◽  
Low Energy ◽  
Trioctylphosphine Oxide ◽  
Reverse Transfer ◽  
Semiconductor Heterostructure ◽  
Ligand Type

The passivation influence by ligands coverage with trioctylphosphine oxide (TOPO) and TOPO including colloidal CdSe/ZnS quantum dots (QDs) on optical properties of the semiconductor heterostructure, namely an array of InP nanowires (NWs) with InAsP nanoinsertion grown by Au-assisted molecular beam epitaxy on Si (111) substrates, was investigated. A significant dependence of the photoluminescence (PL) dynamics of the InAsP insertions on the ligand type was shown, which was associated with the changes in the excitation translation channels in the heterostructure. This change was caused by a different interaction of the ligand shells with the surface of InP NWs, which led to the formation of different interfacial low-energy states at the NW-ligand boundary, such as surface-localized antibonding orbitals and hybridized states that were energetically close to the radiating state and participate in the transfer of excitation. It was shown that the quenching of excited states associated with the capture of excitation to interfacial low-energy traps was compensated by the increasing role of the “reverse transfer” mechanism. As a result, the effectiveness of TOPO-CdSe/ZnS QDs as a novel surface passivation coating was demonstrated.

scholarly journals Photochemical R2PI study of chirality and intermolecular forces in supersonic beam

2001 ◽  
Vol 3 (4) ◽  
pp. 223-227 ◽  
Author(s):  
A. Giardini Guidoni ◽  
S. Piccirillo ◽  
D. Scuderi ◽  
M. Satta ◽  
T. M. Di Palma ◽  
...  
Keyword(s):  
Excited States ◽  
Molecular Beam ◽  
Intermolecular Forces ◽  
Excitation Spectra ◽  
Supersonic Molecular Beam ◽  
Spectral Shifts ◽  
Band Origin ◽  
Solvent Molecules ◽  
The One ◽  
Diastereomeric Complexes

One and two-color, mass selected R2PI spectra of theS1←S0transitions in the bare(+)-(R)- 1-phenyl-1-ethanol(ER) and its complexes with different solvent molecules (solv) (-)-(R)-2-butanol(BR) or(+)-(S)-2-butanol(BS), (—)-(R)-2-pentanol (TR) or(+)-(S)-2-pentanol(TS) and(-)-(R)-2-butylamine(AR) or(+)-(S)-2-butylamine(AS), have been recorded after a supersonic molecular beam expansion. The one-color R2PI excitation spectra of the diastereomeric complexes are characterized by significant shifts of their band origin relative to that of bareER. The extent and the direction of these spectral shifts are found to depend upon the structure and the configuration ofsolvand are attributed to different short-range interactions in the ground and excited states of the complexes. In analogy with other diastereomeric complexes, the phenomenological binding energy of the homochiral cluster is found to be greater than that of the heterochiral one. Preliminary measurements of excitation spectrum of(+)-(R)-1-Indanol(IR) is also reported.

Comparison of the Optical Properties of Er3+ Doped Gallium Nitride Prepared by Metalorganic Molecular Beam Epitaxy (MOMBE) and Solid Source Molecular Beam Epitaxy (SSMBE)

1999 ◽  
Vol 595 ◽  
Author(s):  
U. Hömmerich ◽  
J. T. Seo ◽  
J. D. MacKenzie ◽  
C. R. Abernathy ◽  
R. Birkhahn ◽  
...  
Keyword(s):  
Molecular Beam Epitaxy ◽  
Excited States ◽  
Room Temperature ◽  
Molecular Beam ◽  
Average Lifetime ◽  
Green Luminescence ◽  
Si Substrates ◽  
Lifetime Analysis ◽  
Metalorganic Molecular Beam Epitaxy ◽  
Er Doped

AbstractWe report on the luminescence properties of Er doped GaN grown prepared by metalorganic molecular beam epitaxy (MOMBE) and solid-source molecular beam epitaxy (SSMBE) on Si substrates. Both types of samples emitted characteristic 1.54 µm PL resulting from the intra-4f Er3+ transition 4I13/2→4I15/2. Under below-gap excitation the samples exhibited very similar 1.54 µm PL intensities. On the contrary, under above-gap excitation GaN: Er (SSMBE) showed ∼80 times more intense 1.54 µm PL than GaN: Er (MOMBE). In addition, GaN: Er (SSMBE) also emitted intense green luminescence at 537 nm and 558 nm, which was not observed from GaN: Er (MOMBE). The average lifetime of the green PL was determined to be 10.8 µs at 15 K and 5.5 µs at room temperature. A preliminary lifetime analysis suggests that the decrease in lifetime is mainly due to the strong thermalization between the 2H11/2 and 4S3/2 excited states. Nonradiative decay processes are expected to only weakly affect the green luminescence.

Relevance of the Entropy Factor in Stereoselectivity Control of Asymmetric Photoreactions

Synlett ◽  
2020 ◽  
Vol 31 (13) ◽  
pp. 1259-1267
Author(s):  
Tadashi Mori
Keyword(s):  
Activation Energy ◽  
Excited States ◽  
Weak Interactions ◽  
Supramolecular Interactions ◽  
Thermal Reactions ◽  
Thermodynamics And Kinetics ◽  
Control Concept ◽  
Entropy Factor ◽  
Fine Tune

Entropy as well as enthalpy factors play substantial roles in various chemical phenomena such as equilibrium and reactions. However, the entropy factors are frequently underestimated in most instances, particularly in synthetic chemistry. In reality, the entropy factor can be in competition with the enthalpy factor or can even be decisive in determining the overall free or activation energy change upon molecular interaction and chemical transformation, particularly where weak interactions in ground and/or excited states are significant. In this account, we overview the importance of the entropy factor in various chemical phenomena in both thermodynamics and kinetics and in the ground and excited states. It is immediately apparent that many diastereo- and enantioselective photoreactions are entropy-controlled. Recent advances on the entropy-control concept in asymmetric photoreactions are further discussed. Understanding the entropy-control concept will pave the way to improve, fine-tune, and even invert the chemo- and stereoselectivity of relevant chemical phenomena.1 Introduction2 Role of Entropy in Supramolecular Interactions3 Selected Examples of Entropy-Driven Thermal Reactions4 Classical Examples of Entropy Control in Photoreactions5 Entropy-Driven Asymmetric Photoreactions6 Advances in Entropy Control7 Perspective

HFCN open-shell isomers in solid argon. I. Spectroscopy of the ground and excited states of HFC=N radical

2002 ◽  
Vol 116 (23) ◽  
pp. 10307-10317 ◽  
Author(s):  
Eugenii Ya. Misochko ◽  
Alexander V. Akimov ◽  
Ilya U. Goldschleger ◽  
Charles A. Wight
Keyword(s):  
Excited States ◽  
Open Shell ◽  
Solid Argon
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