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Highly stretchable polymer semiconductor films through the nanoconfinement effect

Jie XuDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USASihong WangDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAGing-Ji Nathan WangDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAChenxin ZhuDepartment of Electrical Engineering, Stanford University, Stanford, CA 94305, USAShaochuan LuoDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, ChinaLihua JinDepartment of Civil and Environmental Engineering, Stanford University, Stanford, CA 94305, USAXiaodan GuDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAShucheng ChenDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAVivian R. FeigDepartment of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USAJohn W. F. ToDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USASimon Rondeau‐GagnéDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAJoonsuk ParkDepartment of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USABob C. SchroederDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAChien LuDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAJin Young OhDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAYanming WangDepartment of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USAYun‐Hi KimDepartment of Chemistry and RINS, Gyeongsang National University, Jinju 660-701, South KoreaHe YanDepartment of Chemistry and Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration & Reconstruction, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong KongRobert SinclairDepartment of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USADongshan ZhouDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, ChinaGi XueDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, ChinaBoris MurmannDepartment of Electrical Engineering, Stanford University, Stanford, CA 94305, USAChristian LinderDepartment of Civil and Environmental Engineering, Stanford University, Stanford, CA 94305, USAWei CaiDepartment of Mechanical Engineering, Stanford University, Stanford, CA 94305, USAJeffrey B.‐H. TokDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAJong Won ChungDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USAZhenan BaoDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305, USA
2017en
ABI

Аннотация

Soft and conformable wearable electronics require stretchable semiconductors, but existing ones typically sacrifice charge transport mobility to achieve stretchability. We explore a concept based on the nanoconfinement of polymers to substantially improve the stretchability of polymer semiconductors, without affecting charge transport mobility. The increased polymer chain dynamics under nanoconfinement significantly reduces the modulus of the conjugated polymer and largely delays the onset of crack formation under strain. As a result, our fabricated semiconducting film can be stretched up to 100% strain without affecting mobility, retaining values comparable to that of amorphous silicon. The fully stretchable transistors exhibit high biaxial stretchability with minimal change in on current even when poked with a sharp object. We demonstrate a skinlike finger-wearable driver for a light-emitting diode.

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Цитирований: 2Использованных источников: 0