Mussel-inspired self-adhesive hydrogels by conducting free radical polymerization in both aqueous phase and micelle phase and their applications in flexible sensors

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL
Shuangli Li , Hongwei Zhou , Yongfei Li , Xilang Jin , Hanbin Liu , Jialiang Lai , Yuanpeng Wu , Weixing Chen , Aijie Ma
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引用次数: 26

Abstract

Polydopamine (PDA)-based self-adhesive hydrogel sensors are extensively explored but it is still a challenge to construct PDA-based hydrogels by free radical polymerization. Herein, a new approach to construct self-adhesive hydrogels by conducting free radical polymerization in both aqueous phase and micelle phase is developed. The following two-phase polymerization processes account for the formation of the self-adhesive hydrogels. The first one is the polymerization of acrylamide (AM) and dopamine (DA) in aqueous phase to form adhesive component PAM-PDA (PAM, polyacrylamide; PDA, polydopamine). The second one is the polymerization of hydrophobic monomer 2-methoxyethyl acrylate (MEA) in micelles of an amphiphilic block copolymer Pluronic F127 diacrylate (F127DA). The poly(2-methoxyethyl acrylate) (PMEA) networks help to maintain the high robustness of the hydrogel. Because PMEA and PDA form in relatively separated phases, the inhibition effect of PDA on the free radical polymerization process of PMEA is weakened. Based on this mechanism, mechanically strong and adhesive hydrogels are achieved. The introduced ions during preparation process, such as Na+, OH and K+, endow the resulting hydrogels ionic conductivity. Resistive strain sensor of the hydrogel achieves a high gauge factor (GF) of 5.26, a response time of 0.25 s and high sensing stability. Because of the adhesiveness, such hydrogel sensor can be applied as wearable sensors in monitoring various human motions. To further address the freezing and drying problems of the hydrogels, organohydrogels are constructed in glycerol-water mixed solvent. The organohydrogels exhibit outstanding anti-freezing property and moisture retention ability, and their adhesiveness is well maintained in subzero conditions. Capacitive pressure sensors of the organohydrogels possessing a GF of 2.05 kPa−1, high sensing stability and reversibility, are demonstrated and explored in monitoring diverse human motions.

Abstract Image

在水相和胶束相进行自由基聚合的贻贝启发自粘水凝胶及其在柔性传感器中的应用
基于聚多巴胺(PDA)的自粘水凝胶传感器已被广泛研究,但利用自由基聚合法制备聚多巴胺水凝胶仍是一个挑战。本文提出了一种在水相和胶束相同时进行自由基聚合制备自粘水凝胶的新方法。以下两相聚合过程解释了自粘水凝胶的形成。第一种是丙烯酰胺(AM)与多巴胺(DA)在水相中聚合形成黏附组分PAM- pda (PAM,聚丙烯酰胺);PDA、polydopamine)。二是疏水单体2-甲氧基乙基丙烯酸酯(MEA)在两亲嵌段共聚物Pluronic F127 diacrylate (F127DA)胶束中的聚合。聚(2-甲氧基乙基丙烯酸酯)(PMEA)网络有助于保持水凝胶的高鲁棒性。由于PMEA和PDA在相对分离的相中形成,PDA对PMEA自由基聚合过程的抑制作用减弱。基于这一机制,可以获得机械强度高、粘接性好的水凝胶。在制备过程中引入的离子,如Na+、OH -和K+,赋予所得水凝胶离子导电性。该水凝胶电阻应变传感器的测量系数(GF)高达5.26,响应时间为0.25 s,具有较高的传感稳定性。由于水凝胶传感器具有粘附性,因此可以作为可穿戴传感器用于监测人体的各种运动。为了进一步解决水凝胶的冷冻和干燥问题,在甘油-水混合溶剂中构建了有机水凝胶。有机水凝胶具有优异的抗冻性和保湿性,在低温条件下也能保持良好的粘接性。有机水凝胶电容式压力传感器的GF为2.05 kPa−1,具有较高的传感稳定性和可逆性,在监测各种人体运动方面得到了验证和探索。
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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