In the broader polymer field, the term ‘crystallinity’ is often used rather loosely. However, increasingly, it becomes critical to clearly distinguish between degree of crystallinity, which provides the fractional amount of crystalline phase in a polymer, and the crystalline quality, which describes the perfection of the crystalline moieties that may form in a polymer. The reason is that these different structural features dictate important properties of plastic materials, including the mechanical properties of commodity polymers and the behavior of macromolecular ferroelectrics; they also determine which photophysical processes occur in semiconducting polymers. Hence, rigor needs to be applied when establishing structure/processing/property interrelations; and it should become a general practice that specific functions are clearly attributed to the degree of crystallinity, the crystalline quality or a combination of the two. In this perspective,
- Award ID(s):
- 1808622
- NSF-PAR ID:
- 10182141
- Date Published:
- Journal Name:
- Annual Review of Materials Research
- Volume:
- 50
- Issue:
- 1
- ISSN:
- 1531-7331
- Page Range / eLocation ID:
- 551 to 574
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract in memoriam of Professor Dick Jones, a long‐time member of IUPAC's Polymer Division, we discuss the challenges of identifying—and distinguishing between—these important structural characteristics when using commonly applied measuring techniques and/or theoretical approaches. This task is often elaborate, as small changes in the chemical nature of the polymer and/or processing conditions selected can have drastic effects on both the crystalline quality and the degree of crystallinity, an issue that combined with the general ambiguity of data obtained with methodologies used to characterize polymer structures, theoretically or experimentally based. © 2023 The Authors.Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry. -
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Abstract Crosslinking is a ubiquitous strategy in polymer engineering to increase the thermomechanical robustness of solid polymers but has been relatively unexplored in the context of π‐conjugated (semiconducting) polymers. Notwithstanding, mechanical stability is key to many envisioned applications of organic electronic devices. For example, the wide‐scale distribution of photovoltaic devices incorporating conjugated polymers may depend on integration with substrates subject to mechanical insult—for example, road surfaces, flooring tiles, and vehicle paint. Here, a four‐armed azide‐based crosslinker (“4Bx”) is used to modify the mechanical properties of a library of semiconducting polymers. Three polymers used in bulk heterojunction solar cells (donors J51 and PTB7‐Th, and acceptor N2200) are selected for detailed investigation. In doing so, it is shown that low loadings of 4Bx can be used to increase the strength (up to 30%), toughness (up to 75%), hardness (up to 25%), and cohesion of crosslinked films. Likewise, crosslinked films show greater physical stability in comparison to non‐crosslinked counterparts (20% vs 90% volume lost after sonication). Finally, the locked‐in morphologies and increased mechanical robustness enable crosslinked solar cells to have greater survivability to four degradation tests: abrasion (using a sponge), direct exposure to chloroform, thermal aging, and accelerated degradation (heat, moisture, and oxygen).
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1146/annurev-matsci-082219-024716
