Liquid metal and Mxene enable self-healing soft electronics based on double networks of bacterial cellulose hydrogels

被引:65
作者
Wang, Ming [1 ,2 ,3 ,4 ]
Rojas, Orlando J. [2 ,3 ,4 ,5 ]
Ning, Like [2 ,3 ,4 ,6 ]
Li, Yuehu [1 ]
Niu, Xun [2 ,3 ,4 ]
Shi, Xuetong [2 ,3 ,4 ]
Qi, Haisong [1 ]
机构
[1] South China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou 510641, Peoples R China
[2] Univ British Columbia, Dept Chem & Biol Engn, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Chem, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Dept Wood Sci, 2360 East Mall, Vancouver, BC V6T 1Z3, Canada
[5] Aalto Univ, Sch Chem Engn, Dept Bioprod & Biosyst, FI-00076 Aalto, Finland
[6] Nanjing Forestry Univ, Coll Chem Engn, Longpan Rd 159, Nanjing 210037, Peoples R China
基金
欧盟地平线“2020”; 加拿大创新基金会;
关键词
Electroactive hydrogels; Liquid metals; Bacterial nanocellulose; Self-healing; Force mapping; FREE-RADICAL POLYMERIZATION; SENSORS;
D O I
10.1016/j.carbpol.2022.120330
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Liquid metal (LM) nanodroplets and MXene nanosheets are integrated with sulfonated bacterial nanocellulose (BNC) and acrylic acid (AA). Upon fast sonication, AA polymerization leads to a crosslinked composite hydrogel in which BNC exfoliates Mxene, forming organized conductive pathways. Soft conducting properties are achieved in the presence of colloidally stable core-shell LM nanodroplets. Due to the unique gelation mechanism and the effect of Mxene, the hydrogels spontaneously undergo surface wrinkling, which improves their electrical sensitivity (GF = 8.09). The hydrogels are further shown to display interfacial adhesion to a variety of surfaces, ultra-elasticity (tailorable elongation, from 1000 % to 3200 %), indentation resistance and self-healing capa-bilities. Such properties are demonstrated in wearable, force mapping, multi-sensing and patternable electro-luminescence devices.
引用
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页数:9
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