{"title":"Tailoring Piezoresistive Behavior of Compressive Strain Sensors by 3D-Printed Structure and Filler Dispersity","authors":"Haidong Yin, Chenyang Zhang, Yu Liu, Fengmei Yu, Ai Lu, Chengzhen Geng","doi":"10.1002/macp.202400480","DOIUrl":null,"url":null,"abstract":"<p>Flexible strain sensors are in high demand for wearable devices and smart healthcare applications. However, compressive strain sensors receive less attention than stretchable counterparts due to their limited sensitivity under compression. Emerging 3D printing technology enables precise control over cellular structures, offering a promising approach to enhance their sensing performance. This study investigates the effects of carbon nanotube (CNT) content, dispersion, and printed structural parameters on 3D-printed polydimethylsiloxane (PDMS)/CNT compressive sensors. Sensors fabricated with 3 wt% CNT ink, prepared via two-roll milling, exhibit a positive resistance change rate under compression, improving sensitivity. The resistance change rate further increases as the printed line spacing decreases and the number of layers increases. Significant variations in sensing behavior, such as resistance increase or decrease under strain, are observed and explained through a unified structural change model. The cyclability of sensors exhibiting different resistance responses is compared, demonstrating the reliability of the optimized sensors for human motion monitoring and spatial force detection. This work deepens the understanding of the piezoresistive behavior of 3D-printed compressive sensors and provides valuable guidance for their design, fabrication, and application.</p>","PeriodicalId":18054,"journal":{"name":"Macromolecular Chemistry and Physics","volume":"226 10","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Chemistry and Physics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/macp.202400480","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Flexible strain sensors are in high demand for wearable devices and smart healthcare applications. However, compressive strain sensors receive less attention than stretchable counterparts due to their limited sensitivity under compression. Emerging 3D printing technology enables precise control over cellular structures, offering a promising approach to enhance their sensing performance. This study investigates the effects of carbon nanotube (CNT) content, dispersion, and printed structural parameters on 3D-printed polydimethylsiloxane (PDMS)/CNT compressive sensors. Sensors fabricated with 3 wt% CNT ink, prepared via two-roll milling, exhibit a positive resistance change rate under compression, improving sensitivity. The resistance change rate further increases as the printed line spacing decreases and the number of layers increases. Significant variations in sensing behavior, such as resistance increase or decrease under strain, are observed and explained through a unified structural change model. The cyclability of sensors exhibiting different resistance responses is compared, demonstrating the reliability of the optimized sensors for human motion monitoring and spatial force detection. This work deepens the understanding of the piezoresistive behavior of 3D-printed compressive sensors and provides valuable guidance for their design, fabrication, and application.
期刊介绍:
Macromolecular Chemistry and Physics publishes in all areas of polymer science - from chemistry, physical chemistry, and physics of polymers to polymers in materials science. Beside an attractive mixture of high-quality Full Papers, Trends, and Highlights, the journal offers a unique article type dedicated to young scientists – Talent.