TY - JOUR
T1 - A design strategy for high mobility stretchable polymer semiconductors
AU - Mun, Jaewan
AU - Ochiai, Yuto
AU - Wang, Weichen
AU - Zheng, Yu
AU - Zheng, Yu Qing
AU - Wu, Hung Chin
AU - Matsuhisa, Naoji
AU - Higashihara, Tomoya
AU - Tok, Jeffrey B.H.
AU - Yun, Youngjun
AU - Bao, Zhenan
N1 - Funding Information:
This work was supported by SAIT, Samsung Electronics Co., Ltd. J.M. acknowledges financial support from Samsung Electronics and Samsung Scholarship. Y.O. was supported by Japan Society for the Promotion of Science (JSPS) Research Fellowship for Young Scientists (Proposal number 18J21080) and Innovative Flex Course for Frontier Organic Material Systems (iFront) at Yamagata University. N.M. was supported by Japan Society for the Promotion of Science (JSPS) overseas research fellowship. Part of this work was performed at the Stanford Nano Shared Facilities (SNSF), supported by the National Science Foundation under award ECCS-1542152. GIXD measurement was carried out at the Stanford Synchrotron Radiation Laboratory (SSRL), a national user facility operated by Stanford University on behalf of the U.S. Department of Energy, Office of Basic Energy Sciences.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - As a key component in stretchable electronics, semiconducting polymers have been widely studied. However, it remains challenging to achieve stretchable semiconducting polymers with high mobility and mechanical reversibility against repeated mechanical stress. Here, we report a simple and universal strategy to realize intrinsically stretchable semiconducting polymers with controlled multi-scale ordering to address this challenge. Specifically, incorporating two types of randomly distributed co-monomer units reduces overall crystallinity and longer-range orders while maintaining short-range ordered aggregates. The resulting polymers maintain high mobility while having much improved stretchability and mechanical reversibility compared with the regular polymer structure with only one type of co-monomer units. Interestingly, the crystalline microstructures are mostly retained even under strain, which may contribute to the improved robustness of our stretchable semiconductors. The proposed molecular design concept is observed to improve the mechanical properties of various p- and n-type conjugated polymers, thus showing the general applicability of our approach. Finally, fully stretchable transistors fabricated with our newly designed stretchable semiconductors exhibit the highest and most stable mobility retention capability under repeated strains of 1,000 cycles. Our general molecular engineering strategy offers a rapid way to develop high mobility stretchable semiconducting polymers.
AB - As a key component in stretchable electronics, semiconducting polymers have been widely studied. However, it remains challenging to achieve stretchable semiconducting polymers with high mobility and mechanical reversibility against repeated mechanical stress. Here, we report a simple and universal strategy to realize intrinsically stretchable semiconducting polymers with controlled multi-scale ordering to address this challenge. Specifically, incorporating two types of randomly distributed co-monomer units reduces overall crystallinity and longer-range orders while maintaining short-range ordered aggregates. The resulting polymers maintain high mobility while having much improved stretchability and mechanical reversibility compared with the regular polymer structure with only one type of co-monomer units. Interestingly, the crystalline microstructures are mostly retained even under strain, which may contribute to the improved robustness of our stretchable semiconductors. The proposed molecular design concept is observed to improve the mechanical properties of various p- and n-type conjugated polymers, thus showing the general applicability of our approach. Finally, fully stretchable transistors fabricated with our newly designed stretchable semiconductors exhibit the highest and most stable mobility retention capability under repeated strains of 1,000 cycles. Our general molecular engineering strategy offers a rapid way to develop high mobility stretchable semiconducting polymers.
UR - http://www.scopus.com/inward/record.url?scp=85107785646&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85107785646&partnerID=8YFLogxK
U2 - 10.1038/s41467-021-23798-2
DO - 10.1038/s41467-021-23798-2
M3 - Article
C2 - 34117254
AN - SCOPUS:85107785646
SN - 2041-1723
VL - 12
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3572
ER -