Robust and Biodegradable Heterogeneous Electronics with Customizable Cylindrical Architecture for Interference-Free Respiratory Rate Monitoring.

Journal: Nano-micro letters
Published Date:

Abstract

A rapidly growing field is piezoresistive sensor for accurate respiration rate monitoring to suppress the worldwide respiratory illness. However, a large neglected issue is the sensing durability and accuracy without interference since the expiratory pressure always coupled with external humidity and temperature variations, as well as mechanical motion artifacts. Herein, a robust and biodegradable piezoresistive sensor is reported that consists of heterogeneous MXene/cellulose-gelation sensing layer and Ag-based interdigital electrode, featuring customizable cylindrical interface arrangement and compact hierarchical laminated architecture for collectively regulating the piezoresistive response and mechanical robustness, thereby realizing the long-term breath-induced pressure detection. Notably, molecular dynamics simulations reveal the frequent angle inversion and reorientation of MXene/cellulose in vacuum filtration, driven by shear forces and interfacial interactions, which facilitate the establishment of hydrogen bonds and optimize the architecture design in sensing layer. The resultant sensor delivers unprecedented collection features of superior stability for off-axis deformation (0-120°, ~ 2.8 × 10 A) and sensing accuracy without crosstalk (humidity 50%-100% and temperature 30-80 °C). Besides, the sensor-embedded mask together with machine learning models is achieved to train and classify the respiration status for volunteers with different ages (average prediction accuracy ~ 90%). It is envisioned that the customizable architecture design and sensor paradigm will shed light on the advanced stability of sustainable electronics and pave the way for the commercial application in respiratory monitory.

Authors

  • Jing Zhang
    MOEMIL Laboratory, School of Optoelectronic Information, University of Electronic Science and Technology of China, Chengdu, China.
  • Wenqi Wang
    School of Life Sciences, Jilin University, Changchun, 130012, China. Electronic address: wangwq18@mails.jlu.edu.cn.
  • Sanwei Hao
    School of Materials Science and Engineering, Shandong University of Technology, Zibo, 255000, People's Republic of China. haosanweixs@163.com.
  • Hongnan Zhu
    Beijing Key Laboratory of Lignocellulosic Chemistry, College of Materials Science and Technology, Beijing Forestry University, Beijing, 100083, People's Republic of China.
  • Chao Wang
    College of Agriculture, Shanxi Agricultural University, Taigu, Shanxi, China.
  • Zhouyang Hu
    Beijing Key Laboratory of Lignocellulosic Chemistry, College of Materials Science and Technology, Beijing Forestry University, Beijing, 100083, People's Republic of China.
  • Yaru Yu
    School of Materials Science and Engineering, Shandong University of Technology, Zibo, 255000, People's Republic of China.
  • Fangqing Wang
    School of Materials Science and Engineering, Shandong University of Technology, Zibo, 255000, People's Republic of China.
  • Peng Fu
    Department of Nuclear Medicine, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China. Electronic address: fupeng0451@163.com.
  • Changyou Shao
    Liaoning Key Laboratory of Lignocellulose Chemistry and Biomaterials, College of Light Industry and Chemical Engineering, Dalian Polytechnic University, Dalian, 116034, People's Republic of China. shaocy@dlpu.edu.cn.
  • Jun Yang
    Cardiovascular Endocrinology Laboratory, Hudson Institute of Medical Research, Clayton, Victoria, Australia; Department of Medicine, Monash University, Clayton, Victoria, Australia.
  • Hailin Cong
    School of Materials Science and Engineering, Shandong University of Technology, Zibo, 255000, People's Republic of China. hailincong@163.com.

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