Stability of Polymer:PCBM Thin Films under Competitive Illumination and Thermal Stress
MECHANISM
Technology
FULLERENES
Chemistry, Multidisciplinary
Materials Science
Materials Science, Multidisciplinary
Condensed Matter
02 engineering and technology
7. Clean energy
09 Engineering
Physics, Applied
HETEROJUNCTION SOLAR-CELLS
Physical
Nanoscience & Nanotechnology
Materials
PHOTODEGRADATION
Multidisciplinary
Science & Technology
photochemistry
02 Physical Sciences
ORGANIC PHOTOVOLTAICS
Chemistry, Physical
Physics
SOLID C-60 FILMS
photovoltaic devices
fullerenes
600
polymeric materials
540
LIFETIMES
PCBM
Chemistry
LIGHT
Physics, Condensed Matter
Applied
Physical Sciences
solar cells
Science & Technology - Other Topics
03 Chemical Sciences
0210 nano-technology
DOI:
10.1002/adfm.201802520
Publication Date:
2018-08-13T14:20:47Z
AUTHORS (5)
ABSTRACT
AbstractThe combined effects of illumination and thermal annealing on the morphological stability and photodimerization in polymer/fullerene thin films are examined. While illumination is known to cause fullerene dimerization and thermal stress their dedimerization, the operation of solar cells involves exposure to both. The competitive outcome of these factors with blends of phenyl‐C61‐butyric acid methyl ester (PCBM) and polystyrene (PS), supported on PEDOT:PSS is quantified. UV–vis spectroscopy is employed to quantify dimerization, time‐resolved neutron reflectivity to resolve the vertical composition stratification, and atomic force microscopy for demixing and coarsening in thin films. At the conventional thermal stress test temperature of 85 °C (and even up to the PS glass transition), photodimerization dominates, resulting in relative morphological stability. Prior illumination is found to result in improved stability upon high temperature annealing, compatible with the need for dedimerization to occur prior to structural relaxation. Modeling of the PCBM surface segregation data suggests that only PCBM monomers are able to diffuse and that illumination provides an effective means to control dimer population, and thus immobile fullerene fraction, in the timescales probed. The results provide a framework for understanding of the stability of organic solar cells under operating conditions.
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CITATIONS (47)
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