电极
离子导入
可穿戴计算机
材料科学
葡萄糖氧化酶
氯化银
纳米技术
生物传感器
工作电极
参比电极
生物医学工程
计算机科学
光电子学
电化学
化学
嵌入式系统
工程类
物理化学
神经科学
生物
作者
Junhao Chen,Yafei Lou,Linan Sun,Chin Hua Chia,Azadeh Nilghaz,Junfei Tian
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2025-02-03
标识
DOI:10.1021/acssensors.4c03277
摘要
Maximizing the efficiency of electrode usage is a crucial step in enhancing the integration of wearables. Currently, electrodes are combined in an additive manner to enable multiplexed sweat screening. The additive sensor requires significant space to accommodate single-function electrodes, which limits the integration of the wearable sensors. Here, we report that the versatility of a single electrode is achieved by assigning different roles to the electrode at different times, resulting in a flexible, disposable, epidermal sweat-sensing platform that integrates in situ iontophoresis and three electrochemical sensors on only four electrodes, while previous platforms required at least seven electrodes. For example, the iontophoresis electrode serves as the working electrode (WE) for chloride sensing and as the counter electrode (CE) for pH sensing after its controllable release of pilocarpine, and the sulfonated polyaniline (SPAN) modified glucose oxidase (GOx) serves as the WE for both pH and glucose sensing. All four functions are integrated into an 8 mm2 (1.8 × 4.45 mm) sensing area, requiring a sample volume of approximately 1 μL. These results open possibility for highly integrated wearable sweat sensors and multimodal sensors.
科研通智能强力驱动
Strongly Powered by AbleSci AI