Heavily n-Dopable π-Conjugated Redox Polymers with Ultrafast Energy Storage Capability

被引:260
作者
Liang, Yanliang [1 ]
Chen, Zhihua [3 ]
Jing, Yan [1 ]
Rong, Yaoguang [1 ]
Facchetti, Antonio [3 ]
Yao, Yan [1 ,2 ]
机构
[1] Univ Houston, Dept Elect & Comp Engn, Houston, TX 77204 USA
[2] Univ Houston, Texas Ctr Superconduct, Houston, TX 77204 USA
[3] Polyera Corp, Skokie, IL 60077 USA
关键词
HIGH-ELECTRON-MOBILITY; SODIUM-ION BATTERIES; CONDUCTING POLYMERS; HIGH-DENSITY; CHARGE; CATHODE; ELECTROCHEMISTRY; THERMOELECTRICS; TRANSPORT; DEVICES;
D O I
10.1021/jacs.5b02290
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report here the first successful demonstration of a pi-conjugated redox polymer simultaneously featuring a pi-conjugated backbone and integrated redox sites, which can be stably and reversibly n-doped to a high doping level of 2.0 with significantly enhanced electronic conductivity. The properties of such a heavily n-dopable polymer, poly{[N,N'-bis(2-octyldodecyl)-1,4,5,8-naphthalenedicarboximide-2,6-diyl]-alt-5,5'-(2,2'-bithiophene)} (P(NDI2OD-T2)), were compared vis-a-vis to those of the corresponding backbone-insulated poly{[N,N'-bis(2-octyldodecyl)-1,4,5,8-naphthalenedicarboximide-2,6-diyl]-alt-5,5'-[2,2'-(1,2-ethanediyl)bithiophene]} (P(NDI2OD-TET)). When evaluated as a charge storage material for rechargeable Li batteries, P(NDI2OD-T2) delivers 95% of its theoretical capacity at a high rate of 100C (72 s per charge-discharge cycle) under practical measurement conditions as well as 96% capacity retention after 3000 cycles of deep discharge-charge. Electrochemical, impedance, and charge-transport measurements unambiguously demonstrate that the ultrafast electrode kinetics of P(NDI2OD-T2) are attributed to the high electronic conductivity of the polymer in the heavily n-doped state.
引用
收藏
页码:4956 / 4959
页数:4
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