Stretchable and Degradable Semiconducting Block Copolymers

被引:72
作者
Sugiyama, Fumitaka [1 ,2 ]
Kleinschmidt, Andrew T. [1 ]
Kayser, Laure V. [1 ]
Alkhadra, Mohammad A. [1 ]
Wan, Jeremy M. -H. [1 ]
Chiang, Andrew S. -C. [1 ]
Rodriquez, Daniel [1 ]
Root, Samuel E. [1 ]
Savagatrup, Suchol [1 ]
Lipomi, Darren J. [1 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, 9500 Gilman Dr,Mail Code 0448, La Jolla, CA 92093 USA
[2] JSR Corp, Minato Ku, 1-9-2 Higashi Shimbashi, Tokyo 1058640, Japan
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ORGANIC SOLAR-CELLS; BAND-GAP POLYMERS; MECHANICAL-PROPERTIES; ELECTRONICS; TRANSISTORS; MOBILITY; ELASTICITY; ELASTOMER; ROBUST; FURAN;
D O I
10.1021/acs.macromol.8b00846
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This paper describes the synthesis and characterization of a class of highly stretchable and degradable semiconducting polymers. These materials are block copolymers (BCPs) in which the semiconducting blocks are based on the diketopyrrolopyrrole (DPP) unit flanked by furan rings and the insulating blocks are poly(epsilon-caprolactone) (PCL). The combination of stiff conjugated segments with flexible aliphatic polyesters produces materials that can be stretched >100%. Remarkably, BCPs containing up to 90 wt % of insulating PCL have the same field-effect mobility as the pure semiconductor. Spectroscopic (ultravioletvisible absorption) and morphological (atomic force microscopic) evidence suggests that the semiconducting blocks form aggregated and percolated structures with increasing content of the insulating PCL. Both PDPP and PCL segments in the BCPs degrade under simulated physiological conditions. Such materials could find use in wearable, implantable, and disposable electronic devices.
引用
收藏
页码:5944 / 5949
页数:6
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