Correction for 'Thermal dissociation of inter-layer excitons in MoS/MoSe hetero-bilayers' by Shinichiro Mouri et al., Nanoscale, 2017, DOI: 10.1039/c7nr01598d.
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Electronic-state chaos, intramolecular electronic energy redistribution, and chemical bonding in persisting multidimensional nonadiabatic systems.
J Chem Phys
August 2023
Fukui Institute for Fundamental Chemistry, Kyoto University, 606-8103 Kyoto, Japan.
We study the chaotic, huge fluctuation of electronic state, resultant intramolecular energy redistribution, and strong chemical bonding surviving the fluctuation with exceedingly long lifetimes of highly excited boron clusters. Those excited states constitute densely quasi-degenerate state manifolds. The huge fluctuation is induced by persisting multidimensional nonadiabatic transitions among the states in the manifold.
View Article and Find Full Text PDFCorrection: Thermal dissociation of inter-layer excitons in MoS/MoSe hetero-bilayers.
Nanoscale
June 2017
Institute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan.
Correction for 'Thermal dissociation of inter-layer excitons in MoS/MoSe hetero-bilayers' by Shinichiro Mouri et al., Nanoscale, 2017, DOI: 10.1039/c7nr01598d.
View Article and Find Full Text PDFThermal dissociation of inter-layer excitons in MoS/MoSe hetero-bilayers.
Nanoscale
May 2017
Institute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan.
We describe photoluminescence (PL), PL excitation, and time-resolved PL spectroscopy of hetero-bilayers comprising monolayers (1L) of MoS and MoSe at cryogenic temperatures. A PL peak showing a decay time of 2.5 ns was observed below 100 K, which can be attributed to an inter-layer exciton emission in the 1L-MoS/1L-MoSe hetero-bilayers.
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Entry of HIV-1 into target cells requires binding of the viral envelope glycoprotein (Env) to cellular receptors and subsequent conformational changes that culminates in fusion of viral and target cell membranes. Recent structural information has revealed that these conformational transitions are regulated by three conserved but potentially flexible layers stacked between the receptor-binding domain (gp120) and the fusion arm (gp41) of Env. We hypothesized that artificial insertion of a covalent bond will 'snap' Env into a conformation that is less mobile and stably expose conserved sites.
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