scholarly journals Carrier Induced Hopping to Band Conduction in Pentacene

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Varsha Rani ◽  
Pramod Kumar ◽  
Akanksha Sharma ◽  
Sarita Yadav ◽  
Budhi Singh ◽  
...  

AbstractCharge transport in organic thin films which are generally polycrystalline is typically limited by the localization of the carriers at lattice defects resulting in low carrier mobilities and carriers move from one state to another state by hopping. However, charge transport in organic semiconductors in their single crystalline phase is coherent due to band conduction and mobilities are not limited by disorder resulting in higher carrier mobility. So it is a challenge to enhance the carrier mobility in a thin film which is the preferred choice for all organic devices. Here, we show that it is possible to increase the carrier mobility in polycrystalline thin films by injecting sufficient carriers such that Fermi level can be moved into the region of high density in Gaussian density of states of molecular solids. When the hopping transport happens through the molecular energy levels whose density is low, mobility is decided by incoherent transport however, when the the hopping transport happens through the energy levels with high density, mobility is decided by coherent transport, as in band conduction. We present results highlighting the observation of both band-like and hopping conduction in polycrystalline organic thin films by varying the concentration of injected charge. More importantly the transition from hopping to band transport is reversible. The observed carrier mobilities in both the regimes match well with theoretical estimates of hopping mobility and band mobility determined from first principles density functional theory.

RSC Advances ◽  
2017 ◽  
Vol 7 (86) ◽  
pp. 54911-54919 ◽  
Author(s):  
Varsha Rani ◽  
Akanksha Sharma ◽  
Pramod Kumar ◽  
Budhi Singh ◽  
Subhasis Ghosh

We investigate the charge transport mechanism in copper phthalocyanine thin films with and without traps. We find that the density of interface states at the grain boundaries can decide the mechanism of charge transport in organic thin films.


Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1188
Author(s):  
Mingu Jang ◽  
Yang-Il Huh ◽  
Mincheol Chang

We systematically studied the influence of solvent vapor annealing on the molecular ordering, morphologies, and charge transport properties of poly(3-hexylthiophene) (P3HT) thin films embedded with preformed crystalline P3HT nanowires (NWs). Solvent vapor annealing (SVA) with chloroform (CF) was found to profoundly impact on the structural and morphological changes, and thus on the charge transport characteristics, of the P3HT-NW-embedded P3HT films. With increased annealing time, the density of crystalline P3HT NWs was increased within the resultant films, and also intra- and intermolecular interactions of the corresponding films were significantly improved. As a result, the P3HT-NW-embedded P3HT films annealed with CF vapor for 20 min resulted in a maximized charge carrier mobility of ~0.102 cm2 V−1 s−1, which is higher than that of pristine P3HT films by 4.4-fold (μ = ~0.023 cm2 V−1 s−1).


1994 ◽  
Vol 08 (07) ◽  
pp. 847-854 ◽  
Author(s):  
Heinz Bässler

The concept of hopping within a Gaussian density of localized states introduced earlier to rationalize charge transport in random organic photoconductors is developed further to account for temporal features of time of flight (TOF) signals. At moderate degree of energetic disorder (σ/kT~3.5…4.5) there is a transport regime intermediate between dispersive and quasi-Gaussian type whose signatures are (i) universal TOF signals that can appear weakly dispersive despite yielding a well defined carrier mobility and (ii) an asymmetric propagator of the carrier packet yielding a time dependent diffusivity.


1990 ◽  
Vol 2 (4) ◽  
pp. 341-342 ◽  
Author(s):  
Yasuhiro Yamaguchi ◽  
Takahiro Fujiyama ◽  
Hiroaki Tanaka ◽  
Masaaki Yokoyama

Química Nova ◽  
2021 ◽  
Author(s):  
Ziran Chen ◽  
Yujin Zhang ◽  
Zhanrong He ◽  
Yuan Li ◽  
Meihao Xi ◽  
...  

Based on density functional theory, quantum chemical calculations of the charge-transport rates were performed for five disc-shaped coronene derivatives with varying numbers of fused thiophene rings, using different basis sets 6-31+G(d) and 6-311++G(d,p), hybrid functionals (B3LYP, M06-2X, CAM-B3LYP, WB97XD, M08-HX), and a dispersion-corrected hybrid functional (M06-2X+D3). Our results indicate that increasing the basis set and adding diffusion and polarisation functions had little effect on the molecular reorganisation energy, charge-transport matrix element t, and charge carrier mobility μ. The charge carrier mobility calculated using B3LYP were relatively large, whereas the results calculated using CAM-B3LYP and WB97XD were similar. Among the five coronene derivatives, molecule b with one thiophene ring could be candidates for a n-type organic semiconductor, and molecule c with two thiophene rings can be designed as a p-type semiconductor.


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