材料科学
聚合物
半导体
纳米技术
可伸缩电子设备
结晶度
单体
光电子学
数码产品
晶体管
复合材料
电气工程
工程类
电压
作者
Jaewan Mun,Yuto Ochiai,Weichen Wang,Yu Zheng,Yu‐Qing Zheng,Hung-Chin Wu,Naoji Matsuhisa,Tomoya Higashihara,Jeffrey B.‐H. Tok,Youngjun Yun,Zhenan Bao
标识
DOI:10.1038/s41467-021-23798-2
摘要
Abstract 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.
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