Ultrafast deposition of polydopamine for high-performance fiber-reinforced high-temperature ceramic composites

被引:8
|
作者
Liu, Yingjun [1 ]
Su, Cheng [1 ]
Zu, Yufei [1 ,2 ]
Chen, Xiaopeng [1 ]
Sha, Jianjun [1 ,2 ]
Dai, Jixiang [1 ,2 ]
机构
[1] Dalian Univ Technol, Key Lab Adv Technol Aerosp Vehicles Liaoning Prov, Dalian 116024, Peoples R China
[2] Dalian Univ Technol, State Key Lab Struct Anal Ind Equipment, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
CONTINUOUS CARBON-FIBER; MECHANICAL-PROPERTIES; C-F/ZRB2-SIC COMPOSITE; ZRB2-BASED COMPOSITES; SURFACE MODIFICATION; DOPAMINE POLYMERIZATION; SLURRY IMPREGNATION; RAPID DEPOSITION; HIGH UNIFORMITY; THIN-FILMS;
D O I
10.1038/s41598-022-24971-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The low deposition time efficiency and small thickness limit the expansion of polydopamine (PDA) application to fiber-reinforced high-temperature ceramic composites. In this work, the electric field-assisted polymerization (EFAP) route was developed to improve the deposition time efficiency of PDA coating and overcome the thickness limitation. Carbonized polydopamine (C-PDA) coating was used as the interphase of carbon fiber-reinforced ZrB2-based composites (C-f/ZrB2-based composite) to bond rigid fibers and brittle ceramics, where C-PDA coating was prepared by the carbonization of PDA coating. Firstly, uniform and dense PDA coatings were deposited on carbon fibers (C-f) by EFAP. The thickness of PDA coating reached the micron level (over 1800 nm) for the first time. Benefiting from the EFAP route promoting the oxidation process of dopamine (DA) and accelerating the aggregation and in-situ polymerization of DA and its derivatives on the surface of C-f, the deposition rate of PDA coating reached 5589 nm/h, which was 3 orders of magnitude higher than that of the traditional self-polymerization process. By adjusting the EFAP parameters (e.g. DA-concentration, current, and deposition time), the thickness of PDA coating could be conveniently designed from nano-scale to micro-scale. Then, PDA coating was pyrolyzed to obtain C-PDA coating. C-PDA coating was well bonded on C-f without visible cross-sticking among neighboring fibers. C-PDA coating presented a layered structure and the thickness of C-PDA coating could be designed by controlling the thickness of PDA. C-PDA coating was used as the interfacial phase of the C-f/ZrB2-based composite, which ensured that the composite possessed good load-bearing capacity and thermal stability. Moreover, extraordinary damage resistance of the composite was achieved, with work of fracture up to 9936 +/- 548 J/m(2) at room temperature and 19,082 +/- 3458 J/m(2) at 1800 degrees C. The current work provides a high time efficiency processing route for depositing PDA coating on carbon fibers and demonstrates the attractive potential of PDA coating in fiber-reinforced high-temperature ceramic composites.
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页数:14
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