4.7 Article

Dynamics of Crystallization and Disorder during Annealing of P3HT/PCBM Bulk Heterojunctions

Journal

MACROMOLECULES
Volume 44, Issue 8, Pages 2725-2734

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma102817z

Keywords

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Funding

  1. Engineering and Physical Sciences Research Council (EPSRC) [EP/F016255, EP/F023200, EP/G031088, EP/F061757, EP/F056710]
  2. Research Councils U.K. (RCUK)
  3. EPSRC [EP/G031088/1, EP/F016255/1, EP/F000375/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/F000375/1, EP/G031088/1, EP/F016255/1] Funding Source: researchfish

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A real-time crystallographic analysis of P3HT/PCBM films during thermal annealing is reported, detailing the temporal variation of crystallization, disorder, and orientational spread during the annealing. Five P3HT/PCBM chlorobenzene solutions with different P3HT concentrations (0, 33, 50, 67, 100 wt %) were spin coated on SiO2 substrates. The thick films (similar to 100 nm) were studied during annealing (50 min at 140 degrees C), with in situ synchrotron grazing incidence X-ray diffraction (GI-XRD) and a sampling time < 8 s. For the first time, the evolution of the crystal structure is analyzed taking into account P3HT paracrystallinity. The following were observed: a predominance of edge-on P3HT lamellae in the as-spun and annealed films; changes in concentration-dependent edge-on lamellar orientation spread along the alkyl-stacking direction and paracrystalline disorder after annealing; a permanent lamellar stretching just along the alky-stacking direction after annealing; an increase in the P3HT domain size along only the alkyl-stacking direction for the edge-on lamellae, with dynamics consistent with PCBM acting as a plasticizer for P3HT; and finally, an increase in the PCBM concentration at the sample-air interface. We show that the paracrystalline correction is important to calculate correctly the domain size as deduced from GI-XRD.

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