材料科学
微尺度化学
制作
自愈水凝胶
执行机构
电场
聚合物
光刻胶
纳米技术
弯曲
电解质
聚电解质
水溶液
工作(物理)
聚合
复合材料
人工肌肉
小型化
纳米棒
微观结构
微电子
阀门执行机构
微技术
实现(概率)
微电子机械系统
光电子学
驻极体
电流体力学
作者
Annaël Sort‐Montenegro,Jason M. Delente,Žiga Roblek,Yekaterina Tskhe,Luke Dowling,Colm Delaney,Larisa Florea
摘要
ABSTRACT Electrically‐driven hydrogels are crosslinked, charged polymer networks that can deform in an electric field, prompted by osmotic pressure changes. To date, such actuators generally suffer from sluggish response time, with equilibrium actuation times ranging from minutes to hours in aqueous electrolytes, and lack sophisticated design, due to established manufacturing protocols. Herein, these limitations are overcome through the fabrication of polyelectrolyte hydrogel microstructures via two‐photon polymerization (2PP). This approach allows for the realization of microscale electrically‐driven actuators exhibiting fast actuation (∼200 ms equilibrium time). The work highlights three photoresist formulations for poly(anionic) and poly(cationic) hydrogel networks and their fabrication via 2PP to produce micro‐electro‐actuators with sub‐micron features. The electrically‐driven actuation performance is investigated by varying the hydrogel composition, actuator geometry, along with electric field strength and direction, and local environment (pH and electrolyte concentration) during actuation. It was determined that micro‐cantilevers of 80 × 20 × 10 µm 3 reached equilibrium bending of up to 44.9 ± 7.8°, in ∼ 200 ms, in response to electric fields of 6 V mm −1 . This pioneering work marks the first integration of 2PP with electrically actuated gelatin‐based hydrogels, showcasing micro‐electro‐actuators with rapid and programmable 4D motion.
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