Unveiling the Molecular Symmetry Dependence of Exciton Dissociation Processes in Small-Molecular Heterojunctions

2018 ◽  
Vol 122 (47) ◽  
pp. 26851-26856 ◽  
Author(s):  
Xian Wang ◽  
Bin Kan ◽  
Zhuoran Kuang ◽  
Hongwei Song ◽  
Guankui Long ◽  
...  
Keyword(s):  
Molecular Symmetry ◽  
Exciton Dissociation ◽  
Molecular Heterojunctions

Double-Excitation Dynamics in m-LPPP probed with sub-20 fs Time Resolution

2003 ◽  
Vol 771 ◽  
Author(s):  
C. Gadermaier ◽  
G. Cerullo ◽  
C. Manzoni ◽  
U. Scherf ◽  
E.J.W. List ◽  
...  
Keyword(s):  
Vibrational Relaxation ◽  
Broad Band ◽  
Generation Efficiency ◽  
Exciton Dissociation ◽  
Charge Generation ◽  
Carrier Generation ◽  
Dissociation Probability ◽  
Ultrafast Relaxation ◽  
First Excited State ◽  
Differential Transmission

AbstractIn a novel modification of transient differential transmission spectroscopy, the first excited state S1 is reexcited via a second laser pulse towards a higher lying state Sn. The dynamics of the relaxation of this state Sn as well as the states created from Sn are revealed by a broad-band probe pulse.We find that the charge carrier generation efficiency from Sn is higher compared to S1. The push and probe durations below 20 fs enable the temporal resolution of the ultrafast relaxation of the Sn state and enables us to identify the two main contributions to enhanced charge generation from Sn, energy migration towards sites of high dissociation probability, and exciton dissociation during vibrational relaxation.

The molecular symmetry of bovine liver catalase

1975 ◽  
Vol 93 (1) ◽  
pp. 55-62 ◽  
Author(s):  
William Eventoff ◽  
G.V. Gurskaya
Keyword(s):  
Bovine Liver ◽  
Molecular Symmetry ◽  
Bovine Liver Catalase

Unraveling the Temperature Dependence of Exciton Dissociation and Free Charge Generation in Nonfullerene Organic Solar Cells

Solar RRL ◽  
2021 ◽  
Vol 5 (4) ◽  
pp. 2000789
Author(s):  
Chao Ma ◽  
Christopher C. S. Chan ◽  
Xinhui Zou ◽  
Han Yu ◽  
Jianquan Zhang ◽  
...  
Keyword(s):  
Solar Cells ◽  
Temperature Dependence ◽  
Organic Solar Cells ◽  
Free Charge ◽  
Exciton Dissociation ◽  
Charge Generation

scholarly journals Phonon-Driven Ultrafast Exciton Dissociation at Donor-Acceptor Polymer Heterojunctions

2008 ◽  
Vol 100 (10) ◽  
Author(s):  
Hiroyuki Tamura ◽  
John G. S. Ramon ◽  
Eric R. Bittner ◽  
Irene Burghardt
Keyword(s):  
Exciton Dissociation ◽  
Donor Acceptor

Studies in aryltin chemistry. Part 6. Crystal and molecular structures of tetra(p-methylsulphonylphenyl)tin(IV) and tetra(p-methylsulphinylphenyl)tin(IV) monohydrate

1990 ◽  
Vol 68 (8) ◽  
pp. 1277-1282 ◽  
Author(s):  
Ivor Wharf ◽  
Michel G. Simard ◽  
Henry Lamparski
Keyword(s):  
Least Squares ◽  
Crystal Structures ◽  
Direct Method ◽  
Molecular Structures ◽  
Water Molecules ◽  
Monoclinic Space Group ◽  
Molecular Symmetry ◽  
Asymmetric Unit ◽  
Full Matrix ◽  
Space Group

Tetrakis(p-methylsulphonylphenyl)tin(IV) and tetrakis(p-methylsulphinylphenyl)tin(IV) n-hydrate have been prepared and their spectra (ir 1350–400 cm−1; nmr, 1H, 13C, 119Sn) and X-ray crystal structures are reported. The first compound is monoclinic, space group C2/c, Z = 4, with a = 21.589(6), b = 6.207(3), c = 22.861(11) Å, β = 93.80(3)° (22 °C); the structure was solved by the direct method and refined by full-matrix least squares calculations to R = 0.043 for 2755 observed reflections. It has 2 molecular symmetry with the methyl group and one oxygen atom completely disordered in both CH3S(O2) groups in the asymmetric unit. The second compound is tetragonal, space group P42/n, Z = 2, with a = b = 15.408(6), c = 6.379(2) Å (−100 °C); the structure was solved by the Patterson method and refined by full-matrix least squares calculations to R = 0.060 for 1209 observed reflections. It has [Formula: see text] molecular symmetry with the whole asymmetric unit disordered. Water molecules occupy positions on parallel 42 axes but molecular packing requirements prevent all sites having 100% occupancy giving n ~ 1 for the hydrate. Keywords: Tetra-aryltins, crystal structures, sulphone, sulphoxide, hydrogen-bonding.

Sign in / Sign up

Export Citation Format

Share Document