• Keine Ergebnisse gefunden

Mott-Wannier Excitons in Inorganic Semiconductors Molecular Excitations Frenkel-Excitons in Molecular Aggregates Exciton-Polaritons, 1D Excitons and others Excitons

N/A
N/A
Protected

Academic year: 2022

Aktie "Mott-Wannier Excitons in Inorganic Semiconductors Molecular Excitations Frenkel-Excitons in Molecular Aggregates Exciton-Polaritons, 1D Excitons and others Excitons"

Copied!
23
0
0

Wird geladen.... (Jetzt Volltext ansehen)

Volltext

(1)

Excitons

Mott-Wannier Excitons in Inorganic Semiconductors Molecular Excitations

Frenkel-Excitons in Molecular Aggregates Exciton-Polaritons, 1D Excitons and others

Dieter Neher, Mai 2015

(2)

Wannier Excitons

Kittel: Festkörperphysik

(3)

One-Electron versus Two-Electron Representation

Yu+Cardona: Fundamentals of Semiconductors

(4)

One-Electron versus Two-Electron Representation

Yu+Cardona: Fundamentals of Semiconductors Kittel: Festkörperphysik

wrong: correct:

(5)

Excitonic Absorption Properties

Yu+Cardona: Fundamentals of Semiconductors

(6)

π -Conjugated Carbon Hydrates

(7)

Molecular Orbitals of Hexatriene

http://wps.prenhall.com/wps/media/objects/724/741576/chapter_01.html

C H2 CH

CH CH

CH CH2

(8)

Ionization Energy

E

LUMO

E

HOMO

+ + e -

Generate positive charge on molecule by removing electron from the molecule IE

Requires Ionization Energy

E

vac

E

Koopmans’ Theorem: IE = - E

HOMO

(9)

Electron Affinity

-

+ e -

Generate negative charge on molecule by placing electron onto the molecule Approximated by donating one electron to the LUMO

EA = -E

LUMO

Releases electron affinity

E

LUMO

E

HOMO

E

vac

E

(10)

Molecular Frenkel Excitons

Occupation of LUMO with one electron

HOMO becomes partially emptied

http://wps.prenhall.com/wps/media/objects/724/741576/chapter_01.html

but this is not a state!!

It is a configuration!!

(11)

The Jablonski Diagram for Molecular Excitations

singlet ground state excited

singlet

states excited

triplet states

Lig ht Ab sor pti on Fl uo re sce nce Pho spho re sce nce

(12)

Exciton Binding Energy

C. Deibel et al., PRB 81, 085202 (2010)

eV

E

G

= 2 . 6 E

S1

= 1 . 9 eV

eV E

b

≅ 0 . 7

Exciton Binding Energy Band absorption hidden below exciton

(13)

Effective Conjugation Length

Nakanishi et al., J. Org. Chem 1998, 63, 8632 Izumi et al., JACS 2003, 125, 5286

relaxed exciton localized over ca. 5 nm along a well defined chain

(14)

Physical Dimers

Pope & Svenberg: Electronic Processes in Organic Crystals and Polymers

(15)

Physical Dimers

General case:

α1 α2

Molekül “1” Molekül “2”

d

3 0

2 1

2 1

12

2

) (

3 ) (

3

d n V n

ε

r

πε

µ µ

µ

µ  −  

=

Point dipole interaction:

Transition dipole moment:

2

1

m

m

M = ±

(16)

Physical Dimers

Distorted crystal of 1,4 dibromonaphthalene

Pope & Svenberg: Electronic Processes in Organic Crystals and Polymers

β = 6.7 cm-1 = 1 meV

(17)

Dispersion of Frenkel Excitons

E. Zojer et al., J. Phys. Cond. Matter. 2000, 12, 1753 e++W’+2β

e++W’-2β e++W’

+π/d -π/d

electron energy loss (EEL) spectrum of a 6P

crystal perp. molecular axis

(18)

Chiral J-Aggregates

R. Marty et al., ACS Nano 2013, 7, 8498

helical nanowires of pi-pi stacked perylene diimides

(19)

Chiral J-Aggregates

R. Marty et al., J. Chem. Phys. B 2014,118, 11152

nanowires exhibit circular dichroism

(20)

J-Aggregates

S.Kirstein and S. Dähne, Int. J. Photoenergy 2006, 20363-1-21

(21)

Exciton Diffusion in J-Aggregates

K. Clark et al., J. Phys. Chem. Lett. 2014, 5, 2274

2 µm 2 µm

excitons diffuse more than 500 nm

(22)

1D Exitons in Polydiacetylene

Y. Lifshitz et al., Phys. Chem.Chem. Phys. 2010, 12, 713 J. Lee et al., Nature Comm. 2014, 5, 3736

http://www.chem.sunysb.edu:81/faculty/jlauher.htm

(23)

1D Exitons in Single Polydiacetylene

F. Dubin et al., Nature Physics 2006, 2, 32

Microphotoluminescence of singly PDA chains in a

diacetylene crystal

Referenzen

ÄHNLICHE DOKUMENTE

The rapidly advancing development of lasers in the 1960s and 70s soon enabled the gen- eration of short laser pulses in the picosecond and femtosecond time domain. 4 Together

The non-Markovianity measure N (Φ) has been used to quantify non-Markovian effects during the quantum evolution of driven systems [53], the spin-boson model [59], biomolecular

Both sets of spectra were fitted with the lineshape model using the SDF defined at 0 K (the SDF itself was different for chlorin and FMO). The modelling was performed as described

Abstract: We demonstrate full charge control, narrow optical linewidths, and optical spin pumping on single self-assembled InGaAs quantum dots embedded in a 162.5 nm thin

Indeed, the standard model (1) overestimates the binding energy by the factor of 4 as well as the level spacing between the lowest and the first excited bound states, which is 8E b /9

If the operator c ␴ † v ␴ 共the part of H pert corresponding to absorption兲 is applied to 兩G典, this contribution results in a state with one hole, a singly occupied c-level

The different be- havior for low and high excitation densities indicates that in fact, two different emission lines are responsible for the observed L 1 /XX peak: at low

Keywords: GaN, nanowire, time-resolved photoluminescence, surface, coalescence, free excitons, bound excitons, radiative recombination, nonradiative recombination, internal