4.7 Article

Cyclotriphosphonitrile-Based Electroactive Flame-Retardant Polymers for Electrochromic/Supercapacitor Devices

Journal

ACS APPLIED POLYMER MATERIALS
Volume 5, Issue 11, Pages 9594-9606

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsapm.3c02043

Keywords

thermal runaway; flame-retardant polymer; cyclotriphosphonitrile; electrochromism; supercapacitor

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To enhance the safety of electrochemical energy storage devices, designing electro-active materials with flame-retardant and thermal insulation functions is considered effective. In this study, a molecular design strategy was proposed to construct intrinsic flame-retardant electro-active materials through the combination of a cyclotriphosphonitrile derivative with a conjugated polymer framework. These materials show dual function capabilities for electrochromic and supercapacitor applications.
To mitigate the thermal runaway issue and thereby enhance the safety of electrochemical energy storage devices, designing electro-active materials with intrinsic flame-retardant and thermal insulation functions is considered an effective way. Herein, we propose an innovative molecular design strategy that amalgamated the cyclotriphosphonitrile derivative HCTP-BTDPBr with a conjugated polymer framework to construct intrinsic flame-retardant electro-active materials serving as dual function electrochromic/supercapacitor applications. Two series of donor-acceptor type copolymers, namely, PrOEG-BTDx-CTPy and PrOC12-BTDx-CTPy, were prepared by carefully modulating the ratio of HCTP-BTDPBr in the whole polymers. Systematic characterization of the electrochemical and flame-retardant performance revealed that PrOEG-BTD0.82-CTP0.18, PrOC12-BTD0.46-CTP0.54, and PrOC12-CTP showed obvious flame-retardant effects with the ignition times of 120, 108, and 80 s alongside heat release rates of 41.9, 27.5, and 31 KW m(-2) g(-1), respectively. The high specific capacitance of 87.34 mF cm(-2) (at 0.1 mA cm(-2)) was obtained from PrOEG-BTD0.82-CTP0.18. Meanwhile, those three copolymers showed excellent electrochromic performance with multiple color changes between blue/transparent, purple/gray, and red-orange/grass green and impressive coloration efficiencies of 258, 158, and 172 cm(2) C1-, respectively. Thus, we believe this molecular design strategy has great potential to improve the safety of electrochemical energy storage devices.

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