Carbon black nanoparticle trapping: a strategy to realize the true energy storage potential of redox-active conjugated microporous polymers

被引:8
|
作者
Kang, Chang Wan [1 ]
Ko, Yoon-Joo [2 ]
Lee, Sang Moon [3 ]
Kim, Hae Jin [3 ]
Choi, Jaewon [4 ,5 ]
Son, Seung Uk [1 ]
机构
[1] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
[2] Seoul Natl Univ, Lab Nucl Magnet Resonance, Natl Ctr Interuniv Res Facil NCIRF, Seoul 08826, South Korea
[3] Korea Basic Sci Inst, Daejeon 34133, South Korea
[4] Gyeongsang Natl Univ, Dept Chem, Jinju 52828, South Korea
[5] Gyeongsang Natl Univ, Res Inst Nat Sci, Jinju 52828, South Korea
基金
新加坡国家研究基金会;
关键词
ORGANIC POLYMERS; PERFORMANCE; HOLLOW; SUPERCAPACITOR; CAPACITANCE; GENERATION; ELECTRODES; MORPHOLOGY; NANOTUBES; REPLICAS;
D O I
10.1039/d1ta04782e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Conjugated microporous polymers (CMPs) have significant potential as electrode materials for electric energy storage devices due to their high surface areas, conjugation features, and chemical stability. However, low conductivity has limited their electrochemical performance. To realize the maximum capability of CMPs, a synthetic strategy for enhancing their conductivity is required. This work shows that during the synthesis of CMPs, carbon black (CB) nanoparticles can be entrapped in situ. Moreover, redox-active benzoquinone (BQ) species could be generated at the CMP to form CMP-BQ through post-synthetic modification. The resultant CB@CMP-BQs with the entrapped CB nanoparticles showed enhanced electrochemical performance as electrode materials for pseudocapacitors, compared with CMP-BQ. They showed capacitances up to 424 and 373 F g(-1) at current densities of 0.5 and 1 A g(-1), respectively. In addition, the optimal CB@CMP-BQ3 showed excellent cycling performance for 10 000 cycles.
引用
收藏
页码:17978 / 17984
页数:7
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