The development of conjugated polymers as the cornerstone of organic electronics

被引:99
作者
Pankow, Robert M. [1 ,2 ]
Thompson, Barry C. [1 ,2 ]
机构
[1] Univ Southern Calif, Dept Chem, Los Angeles, CA 90089 USA
[2] Univ Southern Calif, Loker Hydrocarbon Res Inst, Los Angeles, CA 90089 USA
基金
美国国家科学基金会;
关键词
Conjugated polymers; Organic electronics; Polymer synthesis; Direct arylation polymerization; Organic solar cells; OLED; DIRECT ARYLATION POLYMERIZATION; CATALYZED DIRECT ARYLATION; METALATION-DEPROTONATION MECHANISM; CONTROLLED MOLECULAR-WEIGHT; HETEROJUNCTION SOLAR-CELLS; DONOR-ACCEPTOR COPOLYMERS; FIELD-EFFECT TRANSISTORS; CROSS-COUPLING REACTIONS; THIN-FILM TRANSISTORS; LIGHT-EMITTING-DIODES;
D O I
10.1016/j.polymer.2020.122874
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The expansion of the field of organic electronics has hinged upon structural and fundamental developments in the field of conjugated polymers. Conjugated polymers allow for the manufacture of low-cost, light-weight, flexible organic electronic devices, with notable applications in organic photovoltaics (OPV), organic field effect transistors (OFET), and organic light emitting diodes (OLED). This extraordinary breadth of applications is due to the remarkable diversity of structure, an extensive understanding of structure-function relationships, and the relative ease of structural tuning. Important advancements and the development of such applications is largely due to the evolution of polymer structure, enabled by a broad range of synthetic methods for the tailoring of structures and the development of improved polymerization conditions to limit defects. This perspective provides background from the early days of concerted and focused conjugated polymer research (1970s-1990) to the present, and describes how the tailoring of conjugated polymer structure has now become closely tied to application. A significant focus is also directed to how polymerization methods have evolved from the aggressive, unselective conditions used for oxidative polymerizations to finely tuned transition-metal catalyzed polymerizations that can provide incredibly high structural-fidelity and can proceed through C-H activation. Areas for future work and emerging areas are also discussed, such as high-performing polymers without added structural and synthetic complexity, identifying polymer structures with improved environmental stability, flexible and transient or bioresorbable conjugated polymers, mixed-ion conductors, and photocatalytic and select biological applications.
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页数:23
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