Dynamic dielectric screening and exciton binding energies in conjugated polymers

1997 ◽  
Author(s):  
Jason Weibel ◽  
David Yaron
1999 ◽  
Vol 579 ◽  
Author(s):  
Michael Rohlfing

ABSTRACTWe investigate the formation of excitons in low-dimensional semiconducting systems. To this end a recently developed ab initio approach is employed to determine the excitation energies and optical transition matrix elements of bound and unbound excitonic states. From these results the optical spectrum can be evaluated. We discuss two classes of low- dimensional prototype materials: conjugated polymers and a semiconductor surface. Due to the reduced dimensionality, the excitonic binding energies are much larger than in con- ventional semiconductors.


2021 ◽  
Author(s):  
Ashley Shin ◽  
Azmain A. Hossain ◽  
Stephanie M. Tenney ◽  
Xuanheng Tan ◽  
Lauren A. Tan ◽  
...  

The influence of external dielectric environments is well understood for 2D semiconductor materials but is overlooked for colloidally-grown II-VI nanoplatelets (NPLs). In this work, we synthesize MX (M=Cd, Hg; X= Se, Te) NPLs of varying thicknesses, and apply a modified Elliott model to fit excitonic absorption features and report exciton binding energies for cadmium telluride and mercury chalcogenides for the first time. Our observations indicate that the exciton binding energy is modulated by the dielectric screening of semiconductor material by the external ligand environment. Furthermore, NPL binding energies show a dependence on the number of monolayers consistent with relative effect of internal vs. external dielectric. To describe this, we derive an analytical electrostatic model, reinforcing the hypothesis that the external environment increases the exciton binding energy relative to the bulk—due to the distortion of the Coulombic potential across the NPL surface. We further confirm this effect by decreasing and recovering the exciton binding energy of HgTe NPLs through washing in polarizable solvents. Our results illustrate that NPLs are colloidal analogues of Van der Waals 2D semiconductors and point to surface modification as an approach to control photophysics and device properties.


1997 ◽  
Vol 106 (10) ◽  
pp. 4216-4227 ◽  
Author(s):  
Eric Moore ◽  
Benjamin Gherman ◽  
David Yaron

2004 ◽  
Vol 69 (15) ◽  
Author(s):  
William Barford ◽  
Robert J. Bursill ◽  
David Yaron

2021 ◽  
Author(s):  
Ashley Shin ◽  
Azmain A. Hossain ◽  
Stephanie M. Tenney ◽  
Xuanheng Tan ◽  
Lauren A. Tan ◽  
...  

The influence of external dielectric environments is well understood for 2D semiconductor materials but is overlooked for colloidally-grown II-VI nanoplatelets (NPLs). In this work, we synthesize MX (M=Cd, Hg; X= Se, Te) NPLs of varying thicknesses, and apply a modified Elliott model to fit excitonic absorption features and report exciton binding energies for cadmium telluride and mercury chalcogenides for the first time. Our observations indicate that the exciton binding energy is modulated by the dielectric screening of semiconductor material by the external ligand environment. Furthermore, NPL binding energies show a dependence on the number of monolayers consistent with relative effect of internal vs. external dielectric. To describe this, we derive an analytical electrostatic model, reinforcing the hypothesis that the external environment increases the exciton binding energy relative to the bulk—due to the distortion of the Coulombic potential across the NPL surface. We further confirm this effect by decreasing and recovering the exciton binding energy of HgTe NPLs through washing in polarizable solvents. Our results illustrate that NPLs are colloidal analogues of Van der Waals 2D semiconductors and point to surface modification as an approach to control photophysics and device properties.


Author(s):  
J. Fink

Conducting polymers comprises a new class of materials achieving electrical conductivities which rival those of the best metals. The parent compounds (conjugated polymers) are quasi-one-dimensional semiconductors. These polymers can be doped by electron acceptors or electron donors. The prototype of these materials is polyacetylene (PA). There are various other conjugated polymers such as polyparaphenylene, polyphenylenevinylene, polypoyrrole or polythiophene. The doped systems, i.e. the conducting polymers, have intersting potential technological applications such as replacement of conventional metals in electronic shielding and antistatic equipment, rechargable batteries, and flexible light emitting diodes.Although these systems have been investigated almost 20 years, the electronic structure of the doped metallic systems is not clear and even the reason for the gap in undoped semiconducting systems is under discussion.


Sign in / Sign up

Export Citation Format

Share Document