Liang Yuning, Wu Zixuan, Wei Yaoming, Ding Qiongling, Zilberman Meital, Tao Kai, Xie Xi, Wu Jin
State Key Laboratory of Optoelectronic Materials and Technologies and the Guangdong Province Key Laboratory of Display Material and Technology, School of Electronics and Information Technology, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, 69978, Tel Aviv, Israel.
Nanomicro Lett. 2022 Jan 29;14(1):52. doi: 10.1007/s40820-021-00787-0.
With the advent of the 5G era and the rise of the Internet of Things, various sensors have received unprecedented attention, especially wearable and stretchable sensors in the healthcare field. Here, a stretchable, self-healable, self-adhesive, and room-temperature oxygen sensor with excellent repeatability, a full concentration detection range (0-100%), low theoretical limit of detection (5.7 ppm), high sensitivity (0.2%/ppm), good linearity, excellent temperature, and humidity tolerances is fabricated by using polyacrylamide-chitosan (PAM-CS) double network (DN) organohydrogel as a novel transducing material. The PAM-CS DN organohydrogel is transformed from the PAM-CS composite hydrogel using a facile soaking and solvent replacement strategy. Compared with the pristine hydrogel, the DN organohydrogel displays greatly enhanced mechanical strength, moisture retention, freezing resistance, and sensitivity to oxygen. Notably, applying the tensile strain improves both the sensitivity and response speed of the organohydrogel-based oxygen sensor. Furthermore, the response to the same concentration of oxygen before and after self-healing is basically the same. Importantly, we propose an electrochemical reaction mechanism to explain the positive current shift of the oxygen sensor and corroborate this sensing mechanism through rationally designed experiments. The organohydrogel oxygen sensor is used to monitor human respiration in real-time, verifying the feasibility of its practical application. This work provides ideas for fabricating more stretchable, self-healable, self-adhesive, and high-performance gas sensors using ion-conducting organohydrogels.
随着5G时代的到来和物联网的兴起,各种传感器受到了前所未有的关注,尤其是医疗保健领域中的可穿戴和可拉伸传感器。在此,通过使用聚丙烯酰胺-壳聚糖(PAM-CS)双网络(DN)有机水凝胶作为新型传感材料,制备了一种具有出色重复性、全浓度检测范围(0-100%)、低理论检测限(5.7 ppm)、高灵敏度(0.2%/ppm)、良好线性以及优异的温度和湿度耐受性的可拉伸、自愈合、自粘附且室温的氧气传感器。PAM-CS DN有机水凝胶是通过简便的浸泡和溶剂置换策略由PAM-CS复合水凝胶转变而来。与原始水凝胶相比,DN有机水凝胶表现出大大增强的机械强度、保湿性、抗冻性以及对氧气的敏感性。值得注意的是,施加拉伸应变可提高基于有机水凝胶的氧气传感器的灵敏度和响应速度。此外,自愈合前后对相同浓度氧气的响应基本相同。重要的是,我们提出了一种电化学反应机理来解释氧气传感器的正电流偏移,并通过合理设计的实验证实了这种传感机理。该有机水凝胶氧气传感器用于实时监测人体呼吸,验证了其实际应用的可行性。这项工作为使用离子导电有机水凝胶制造更多可拉伸、自愈合、自粘附且高性能的气体传感器提供了思路。