Highly Sensitive Flexible Tactile Sensor Mimicking the Microstructure Perception Behavior of Human Skin
Source abstract
Abstract
A 3D printed flexible tactile sensor with graphene–polydimethylsiloxane (PDMS) microspheres for microstructure perception is presented. The structure of the tactile sensor is inspired by the texture of the human finger and is designed to enable the detection of various levels of surface roughness via the processing of tactile signals. The tactile sensor with a unique graphene–PDMS microsphere structure shows excellent comprehensive mechanical properties, including a robust stretching ability (elongation at break of the sensing layer is 70%), excellent sensing ability (short response time of 60 ms), high sensitivity (sensitivity up to 2.4 kPa–1), and cycle stability (over 2000 loading cycles). In addition, such versatility and sensitivity allow the electronic skin not only to accurately monitor pressure but also to distinguish various surface topographies with microscale differences, and to detect the action of an air fluid.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Tactile and Sensory Interactions · Interactive and Immersive Displays
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Laboratory for Advanced Lubricating Materials, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China
University of Chinese Academy of Sciences, Beijing 100049, China
Division of Engineering in Medicine, Brigham and Women’s Hospital, Harvard Medical School, Cambridge, Massachusetts 02139, United States
Funding
Natural Science Foundation of Shanghai · China Scholarship Council · National Natural Science Foundation of China
References (42)
Show source-provided references
1. 10.1002/adma.20150422510.1002/adma.201504225 ↗
2. 10.1021/nn505953t10.1021/nn505953t ↗
3. 10.1002/adma.20150495810.1002/adma.201504958 ↗
4. 10.1002/adma.20130224010.1002/adma.201302240 ↗
5. 10.1002/adma.20170121810.1002/adma.201701218 ↗
6. 10.1038/nmat478210.1038/nmat4782 ↗
7. 10.1002/adma.20090274010.1002/adma.200902740 ↗
8. 10.1002/adma.20150511810.1002/adma.201505118 ↗
9. 10.1002/adem.20170034110.1002/adem.201700341 ↗
10. 10.1002/adma.20170155410.1002/adma.201701554 ↗
11. 10.1002/adma.20119009210.1002/adma.201190092 ↗
12. 10.1002/adma.20140180410.1002/adma.201401804 ↗
13. 10.1002/adma.20190283110.1002/adma.201902831 ↗
14. 10.1002/admt.20190014710.1002/admt.201900147 ↗
15. 10.1021/acsami.7b0961710.1021/acsami.7b09617 ↗
16. 10.1002/adma.20160675510.1002/adma.201606755 ↗
17. 10.1038/nmat245910.1038/nmat2459 ↗
18. 10.1002/smll.20160141910.1002/smll.201601419 ↗
19. 10.1088/0960-1317/21/11/11501210.1088/0960-1317/21/11/115012 ↗
20. 10.1002/adma.20147005410.1002/adma.201470054 ↗
21. 10.1021/nl300988z10.1021/nl300988z ↗
22. 10.1088/0957-4484/24/44/44400610.1088/0957-4484/24/44/444006 ↗
23. 10.1002/adfm.20167005110.1002/adfm.201670051 ↗
24. 10.1021/acs.chemrev.7b0029110.1021/acs.chemrev.7b00291 ↗
25. 10.1021/acsami.7b0197910.1021/acsami.7b01979 ↗
26. 10.1002/adma.20170370010.1002/adma.201703700 ↗
27. 10.1002/adma.20170267510.1002/adma.201702675 ↗
28. 10.1038/ncomms822110.1038/ncomms8221 ↗
29. 10.1038/nmat283410.1038/nmat2834 ↗
30. 10.1002/smll.20140120710.1002/smll.201401207 ↗
31. 10.1038/nmat338010.1038/nmat3380 ↗
32. 10.1002/smll.20180081910.1002/smll.201800819 ↗
33. 10.1016/j.eml.2016.05.01510.1016/j.eml.2016.05.015 ↗
34. 10.1126/science.125422910.1126/science.1254229 ↗
35. 10.1152/jn.1996.75.6.233410.1152/jn.1996.75.6.2334 ↗
36. 10.1002/adma.20130518210.1002/adma.201305182 ↗
37. 10.1021/acsami.5b0382410.1021/acsami.5b03824 ↗
38. 10.1038/ncomms400210.1038/ncomms4002 ↗
39. 10.1002/adfm.20170750310.1002/adfm.201707503 ↗
40. 10.1126/sciadv.aay284010.1126/sciadv.aay2840 ↗
41. 10.1111/j.0909-725X.2006.00126.x10.1111/j.0909-725X.2006.00126.x ↗
42. Kandel E. R. · 2012