Molecular ordering of spin-coated and electrosprayed P3HT:PCBM thin films and their applications to photovoltaic cell
Creators
- 1. Department of Functional Materials Science, Saitama University, 255 Shimo-Okubo, Sakura-ku, Saitama 338-8570 (Japan)
- 2. CERMAV-CNRS, UPR5301 & Grenoble Alpes University, 601 rue de la Chimie, BP53, 38041 Grenoble Cedex 9 (France)
- 3. Emergent Molecular Function Research Group, RIKEN Center for Emergent Matter Science (CEMS), Wako, Saitama 351-0198 (Japan)
Description
Poly(3-hexylthiophene-2,5-diyl) (P3HT) is one of the most popular donor polymers for organic photovoltaic cells; however, annealing-induced molecular ordering is necessary for realizing high photoconversion efficiency. In this study, the ratio of ordered-disordered P3HT Raman signals was calculated as the crystallinity parameter, which can be evaluated as the molecular ordering of P3HT. In the case of spin-coated devices, the crystallinity parameter increases with increasing annealing temperature, and this agrees with the photovoltaic performance. Furthermore, the direct molecular ordering of P3HT during electrospray deposition is reported, detailing the relation between the solvent evaporation time and the crystallinity of P3HT, and is evaluated by Raman spectroscopy and grazing incidence X-ray diffraction. To observe the solvent evaporation phenomena of the electropsray process, in situ measurement of solvent evaporation time was also successfully realized for the first time by placing a CCD camera below the substrate in electrospray deposition. The solvent evaporation time was controlled from 0.036 to 2.8 s by changing the applied voltage and solvent. By investigating the relationship between the solvent evaporation time and the molecular ordering of P3HT, the long solvent evaporation time caused the high crystallinity of P3HT. In addition, the population of P3HT crystallinity with an edge-on orientation also increased with increasing solvent evaporation time by evaluating the grazing incidence X-ray diffraction pattern, in good agreement with the estimated crystallinity from Raman spectroscopy. Finally, a photoconversion efficiency of 2.0% was achieved by electrospray deposition without post thermal annealing. - Highlights: • An orientation of P3HT was controlled due to the solvent evaporation time. • A solvent evaporation time was evaluated for the electrospray deposition. • A crystallinity parameter was evaluated from the Raman spectroscopy. • X-ray diffraction indicates the increased edge-on oriented P3HT. • A photo conversion efficiency of2.0% was achieved without the annealing.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.tsf.2016.06.019Additional details
Identifiers
- DOI
- 10.1016/j.tsf.2016.06.019;
- PII
- S0040-6090(16)30262-0;
Publishing Information
- Journal Title
- Thin Solid Films
- Journal Volume
- 612
- Journal Page Range
- p. 373-380
- ISSN
- 0040-6090
- CODEN
- THSFAP
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48021030
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ANNEALING; CHARGE-COUPLED DEVICES; CRYSTALLIZATION; DEPOSITION; ELECTRIC POTENTIAL; EVAPORATION; ORGANIC POLYMERS; PHOTOVOLTAIC CELLS; PHOTOVOLTAIC EFFECT; RAMAN SPECTROSCOPY; SOLVENTS; SPIN; SUBSTRATES; THIN FILMS; THIOPHENE; X-RAY DIFFRACTION
- Descriptors DEC
- ANGULAR MOMENTUM; COHERENT SCATTERING; DIFFRACTION; DIRECT ENERGY CONVERTERS; FILMS; HEAT TREATMENTS; HETEROCYCLIC COMPOUNDS; LASER SPECTROSCOPY; ORGANIC COMPOUNDS; ORGANIC SULFUR COMPOUNDS; PARTICLE PROPERTIES; PHASE TRANSFORMATIONS; PHOTOELECTRIC CELLS; PHOTOELECTRIC EFFECT; POLYMERS; SCATTERING; SEMICONDUCTOR DEVICES; SPECTROSCOPY
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.