Intrinsically Stretchable Block Copolymer Based on PEDOT:PSS for Improved Performance in Bioelectronic Applications

被引:41
|
作者
Blau, Rachel [1 ]
Chen, Alexander X. [1 ]
Polat, Beril [1 ]
Becerra, Laura L. [1 ]
Runser, Rory [1 ]
Zamanimeymian, Beeta [1 ]
Choudhary, Kartik [1 ]
Lipomi, Darren J. [1 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
PEDOT:PSS; organic electronics; stretchable electronics; electromyography (EMG); RAFT polymerization; block copolymers; CONDUCTIVITY ENHANCEMENT; TRANSPARENT ELECTRODES; MECHANICAL-PROPERTIES; RAFT POLYMERIZATION; SOLAR-CELLS; THIN-FILMS; PSS; MORPHOLOGY; TRANSISTORS; EFFICIENCY;
D O I
10.1021/acsami.1c18495
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The conductive polyelectrolyte complex poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is ubiquitous in research dealing with organic electronic devices (e.g., solar cells, wearable and implantable sensors, and electrochemical transistors). In many bioelectronic applications, the applicability of commercially available formulations of PEDOT:PSS (e.g., Clevios) is limited by its poor mechanical properties. Additives can be used to increase the compliance but pose a risk of leaching, which can result in device failure and increased toxicity (in biological settings). Thus, to increase the mechanical compliance of PEDOT:PSS without additives, we synthesized a library of intrinsically stretchable block copolymers. In particular, controlled radical polymerization using a reversible addition-fragmentation transfer process was used to generate block copolymers consisting of a block of PSS (of fixed length) appended to varying blocks of poly(poly(ethylene glycol) methyl ether acrylate) (PPEGMEA). These block copolymers (PSS(1)-b-PPEGMEA((alpha)), where x ranges from 1 to 6) were used as scaffolds for oxidative polymerization of PEDOT. By increasing the lengths of the PPEGMEA segments on the PEDOT:[PSS(1)-b-PPEGMEA((1-6))] block copolymers, ("Block-1" to "Block-6"), or by blending these copolymers with PEDOT:PSS, the mechanical and electronic properties of the polymer can be tuned. Our results indicate that the polymer with the longest block of PPEGMEA, Block-6, had the highest fracture strain (75%) and lowest elastic modulus (9.7 MPa), though at the expense of conductivity (0.01 S cm(-1)). However, blending Block-6 with PEDOT:PSS to compensate for the insulating nature of the PPEGMEA resulted in increased conductivity [2.14 S cm(-1) for Blend-6 (2:1)]. Finally, we showed that Block-6 outperforms a commercial formulation of PEDOT:PSS as a dry electrode for surface electromyography due to its favorable mechanical properties and better adhesion to skin.
引用
收藏
页码:4823 / 4835
页数:13
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