期刊
NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -出版社
NATURE RESEARCH
DOI: 10.1038/s41467-020-14656-8
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资金
- National Science Foundation [DMR-1629006, DMR-1921854]
The glass transition temperature (T-g) is a key property that dictates the applicability of conjugated polymers. The T-g demarks the transition into a brittle glassy state, making its accurate prediction for conjugated polymers crucial for the design of soft, stretchable, or flexible electronics. Here we show that a single adjustable parameter can be used to build a relationship between the T-g and the molecular structure of 32 semiflexible (mostly conjugated) polymers that differ drastically in aromatic backbone and alkyl side chain chemistry. An effective mobility value zeta, is calculated using an assigned atomic mobility value within each repeat unit. The only adjustable parameter in the calculation of zeta is the ratio of mobility between conjugated and non-conjugated atoms. We show that. correlates strongly to the T-g, and that this simple method predicts the T-g with a root-mean-square error of 13 degrees C for conjugated polymers with alkyl side chains.
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