Exciton transport in organic semiconductors: Förster resonance energy transfer compared with a simple random walk

Forster resonance energy transfer theory (FRET) and a simple random walk (RW) are both implemented in a dynamic Monte Carlo simulation with the aim of determining the exciton diffusion length from photoluminescence (PL) measurements. The calculated diffusion lengths obtained from both models are shown to be the same. As such, given that the computational time of a random walk is typically 2–3 orders of magnitude smaller than the FRET approach, this work shows that the RW methodology can be a preferable model for the determination of diffusion lengths. We also show that the RW approach may also be implemented in Monte Carlo simulations that describe organic solar cells. Despite the fact that (compared with FRET) RW does not account for non-nearest neighbor hopping or energy relaxation, we show that the resulting overestimation of the simulated current will not exceed 2% for typical OPV parameters. In addition, by taking advantage of the gain in speed we are able to investigate the impact of the exciton dif...

[1]  Xiaoniu Yang,et al.  Toward High-Performance Polymer Solar Cells: The Importance of Morphology Control , 2007 .

[2]  Lingyi Meng,et al.  Dynamic Monte Carlo simulation for highly efficient polymer blend photovoltaics. , 2010, The journal of physical chemistry. B.

[3]  A. Walker,et al.  Dynamical Monte Carlo modelling of organic solar cells: the dependence of internal quantum efficiency on morphology. , 2005, Nano letters.

[4]  Jianyong Ouyang,et al.  Polymer Optoelectronic Devices with High‐Conductivity Poly(3,4‐Ethylenedioxythiophene) Anodes , 2004 .

[5]  Fan Yang,et al.  Photocurrent generation in nanostructured organic solar cells. , 2008, ACS nano.

[6]  Stephen R. Forrest,et al.  Small molecular weight organic thin-film photodetectors and solar cells , 2003 .

[7]  Guido Raos,et al.  Methodological assessment of kinetic Monte Carlo simulations of organic photovoltaic devices: the treatment of electrostatic interactions. , 2010, The Journal of chemical physics.

[8]  D. Gillespie A General Method for Numerically Simulating the Stochastic Time Evolution of Coupled Chemical Reactions , 1976 .

[9]  W. Stampor,et al.  Photogeneration of charge in solid films of α-sexithiophene , 1998 .

[10]  H. Bässler,et al.  What controls triplet exciton transfer in organic semiconductors , 2011 .

[11]  R. Dillon,et al.  Electronic energy migration on different time scales: concentration dependence of the time-resolved anisotropy and fluorescence quenching of Lumogen Red in poly(methyl methacrylate). , 2010, The journal of physical chemistry. A.

[12]  D. L. Dexter A Theory of Sensitized Luminescence in Solids , 1953 .

[13]  Neil C. Greenham,et al.  A microscopic model for the behavior of nanostructured organic photovoltaic devices , 2007 .

[14]  S. Forrest,et al.  Exciton diffusion lengths of organic semiconductor thin films measured by spectrally resolved photoluminescence quenching , 2009 .

[15]  N. Greenham,et al.  Monte Carlo modeling of geminate recombination in polymer-polymer photovoltaic devices. , 2008, The Journal of chemical physics.

[16]  V. Bulović,et al.  Modeling of exciton diffusion in amorphous organic thin films. , 2006, Physical review letters.

[17]  N. Greenham,et al.  Effect of charge trapping on geminate recombination and polymer solar cell performance. , 2010, Nano letters.

[18]  X. Ding,et al.  Exciton migration in organic thin films , 2006 .

[19]  Joop Schoonman,et al.  Photoluminescence study of sexithiophene thin films. , 2005, The journal of physical chemistry. B.

[20]  Stephen R. Forrest,et al.  Efficient bulk heterojunction photovoltaic cells using small-molecular-weight organic thin films , 2003, Nature.

[21]  Jpl John Segers,et al.  Efficient Monte Carlo methods for the simulation of catalytic surface reactions , 1998 .

[22]  Thomas,et al.  Monte Carlo study of picosecond exciton relaxation and dissociation in poly(phenylenevinylene). , 1996, Physical review. B, Condensed matter.

[23]  David Beljonne,et al.  Exciton diffusion in energetically disordered organic materials , 2009 .

[24]  M. Knupfer,et al.  Size and dispersion of excitons in organic semiconductors , 2004 .