Enhanced thermal conductivity in copolymerized polyimide.
Enhanced thermal conductivity in copolymerized polyimide.
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DOI:
10.1016/j.isci.2022.105451
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发表时间:
2022-11-18
期刊:
影响因子:
5.8
通讯作者:
Xu, Xiangfan
中科院分区:
文献类型:
--
作者:
Liu, Bohai;Zhou, Yu;Dong, Lan;Lu, Qinghua;Xu, Xiangfan
From flexible electronics and multifunctional textiles to artificial tissues, polymers penetrate nearly every aspect of modern technology. High thermal conductivity of polymers is often required in their applications, where heat dissipation is crucial to maintain product reliability and functionality. However, the intrinsic thermal conductivity of bulk polymers is largely hindered by the randomly coiled and entangled chain conformation. Here, we report a copolymerization strategy that can simultaneously manipulate the intrachain and interchain hopping and increase the thermal conductivity of linear copolymerized polyimide (PI) to three times higher than that of pure PI at a low-level introduction of 2,4,5,7-tetraamino-1,8-dihydroxyanthracene-9,10-dione (10%). In addition, the large-scale copolymerized PI films display thermal stability after annealing. These remarkable results allow bulk PI to be a potential candidate for thermal management, and this copolymerization method may benefit future synthesis of interfacial thermal materials. A copolymerization method to fabricate large-sized and thermally stable PI films The intrachain and interchain hopping in the copolymer can be simultaneously enhanced Thermal conductivity of copolymerized PI films is about 3x higher than that in pure PI Polymer chemistry; Thermal property; Polymers
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