Molecular Weight Dependent Charge Carrier Mobility in Poly(3,3‘ ‘-dioctyl-2,2‘:5‘,2‘ ‘-terthiophene)

2006 ◽  
Vol 110 (27) ◽  
pp. 13305-13309 ◽  
Author(s):  
Jean-Marie Verilhac ◽  
Rafal Pokrop ◽  
Gilles LeBlevennec ◽  
Irena Kulszewicz-Bajer ◽  
Katarzyna Buga ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Charge Carrier ◽  
Carrier Mobility ◽  
Charge Carrier Mobility

scholarly journals Perovskite solar cells involving poly(tetraphenylbenzidine)s: investigation of hole carrier mobility, doping effects and photovoltaic properties

RSC Advances ◽  
2014 ◽  
Vol 4 (82) ◽  
pp. 43550-43559 ◽  
Author(s):  
Katharina Neumann ◽  
Mukundan Thelakkat
Keyword(s):  
Molecular Weight ◽  
Solar Cells ◽  
Charge Carrier ◽  
Carrier Mobility ◽  
Perovskite Solar Cells ◽  
Charge Carrier Mobility ◽  
Hole Transport ◽  
Photovoltaic Properties ◽  
Doping Effects

A detailed study on the important properties of poly(tetraphenylbenzidine) as hole transport material in perovskite solar cells such as the influence of the molecular weight, the doping effects on charge carrier mobility and the polarity of the material is presented.

The Influence of Nitrogen Position on Charge Carrier Mobility in Enantiopure Aza[6]helicene Crystals

2018 ◽  
Author(s):  
Francesco Salerno ◽  
Beth Rice ◽  
Julia Schmidt ◽  
Matthew J. Fuchter ◽  
Jenny Nelson ◽  
...  
Keyword(s):  
Solid State ◽  
Charge Carrier ◽  
Carrier Mobility ◽  
Chemical Structure ◽  
Crystal Packing ◽  
Charge Carrier Mobility ◽  
Individual Factor ◽  
Charge Mobility ◽  
Order Of Magnitude ◽  
Small Change

<p>The properties of an organic semiconductor are dependent on both the chemical structure of the molecule involved, and how it is arranged in the solid-state. It is challenging to extract the influence of each individual factor, as small changes in the molecular structure often dramatically change the crystal packing and hence solid-state structure. Here, we use calculations to explore the influence of the nitrogen position on the charge mobility of a chiral organic molecule when the crystal packing is kept constant. The transfer integrals for a series of enantiopure aza[6]helicene crystals sharing the same packing were analysed in order to identify the best supramolecular motifs to promote charge carrier mobility. The regioisomers considered differ only in the positioning of the nitrogen atom in the aromatic scaffold. The simulations showed that even this small change in the chemical structure has a strong effect on the charge transport in the crystal, leading to differences in charge mobility of up to one order of magnitude. Some aza[6]helicene isomers that were packed interlocked with each other showed high HOMO-HOMO integrals (up to 70 meV), whilst molecules arranged with translational symmetry generally afforded the highest LUMO-LUMO integrals (40 - 70 meV). As many of the results are not intuitively obvious, a computational approach provides additional insight into the design of new semiconducting organic materials.</p>

Assembly effect on the charge carrier mobility in quaterthiophene-based n/p-materials

2019 ◽  
Vol 7 (22) ◽  
pp. 6649-6655
Author(s):  
A. López-Andarias ◽  
C. Atienza ◽  
J. López-Andarias ◽  
W. Matsuda ◽  
T. Sakurai ◽  
...  
Keyword(s):  
Charge Carrier ◽  
Self Assembly ◽  
Carrier Mobility ◽  
Charge Carrier Mobility ◽  
Assembly Process ◽  
Charge Mobility

Effect of the peptide-based quaterthiophene self-assembly process on the charge mobility properties of the n/p-materials formed is studied.

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