Highly Aligned Carbon Nanotube‐Based Bi‐Material Microactuators with Reduced Intertube Slipping
Source abstract
Abstract
Abstract Bi‐material microcantilevers have been widely used as both thermal sensors and thermal actuators. Carbon nanotubes (CNT) are prominent candidates for bi‐material actuators due to the negative coefficient of thermal expansion (CTE) at the axial direction that allows for higher thermal sensitivity. However, CNT‐based actuators generally suffer not only from intertube slipping due to weak interactions between the assembled CNTs but also from poor control over orientation assembly. To address these challenges, a new class of closely packed, highly aligned CNT microcantilevers reinforced by ceramic interlocking is here proposed, followed with deposition of Al thin film to form the bi‐material actuators. The investigations of the mechanical properties and thermal response of CNT microcantilevers indicate that the slipping between the tubes limits both the strength and the thermal sensitivity of the bi‐material microcantilevers. Intertube deposition of Al2O3 as ceramic interlocking is used to reinforce the binding strength between the tubes, and increases in the mechanical strength as well as thermal sensitivity of the microcantilevers have been achieved.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Carbon Nanotubes in Composites · Mechanical and Optical Resonators · Transition Metal Oxide Nanomaterials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CAS Key Laboratory of Mechanical Behavior and Design of Materials University of Science and Technology of China Hefei Anhui 230027 P. R. China
Department of Precision Machinery and Precision Instrumentation University of Science and Technology of China Hefei Anhui 230027 P. R. China
Funding
National Natural Science Foundation of China
References (31)
Show source-provided references
1. Conley H. · Nano Lett. · 2011 · 11
2. 10.1002/adma.20180638610.1002/adma.201806386 ↗
3. 10.1021/nl303405g10.1021/nl303405g ↗
4. 10.1021/acs.nanolett.6b0439310.1021/acs.nanolett.6b04393 ↗
5. 10.1021/nl103618e10.1021/nl103618e ↗
6. 10.1103/PhysRevLett.92.01590110.1103/PhysRevLett.92.015901 ↗
7. 10.1016/j.nanoen.2019.10430210.1016/j.nanoen.2019.104302 ↗
8. 10.1073/pnas.090015510610.1073/pnas.0900155106 ↗
9. 10.1021/acs.jpcc.5b1267310.1021/acs.jpcc.5b12673 ↗
10. 10.1002/adma.20110054710.1002/adma.201100547 ↗
11. 10.1038/nmat107610.1038/nmat1076 ↗
12. 10.1016/j.nimb.2012.12.11110.1016/j.nimb.2012.12.111 ↗
13. 10.1002/adfm.20120135810.1002/adfm.201201358 ↗
14. 10.1016/j.compositesa.2016.10.01610.1016/j.compositesa.2016.10.016 ↗
15. 10.1088/1361-665X/aac07710.1088/1361-665X/aac077 ↗
16. 10.3390/nano809073210.3390/nano8090732 ↗
17. 10.1038/nnano.2008.9810.1038/nnano.2008.98 ↗
18. 10.1021/nl301647210.1021/nl3016472 ↗
19. 10.1088/0957-4484/24/47/47570710.1088/0957-4484/24/47/475707 ↗
20. 10.1002/adfm.20150367310.1002/adfm.201503673 ↗
21. 10.1002/1521-396X(200210)193:3<R13::AID-PSSA999913>3.0.CO;2-Z10.1002/1521-396X(200210)193:3<R13::AID-PSSA999913>3.0.CO;2-Z ↗
22. 10.1038/2160710.1038/21607 ↗
23. 10.1038/414773a10.1038/414773a ↗
24. 10.1016/S0266-3538(03)00064-210.1016/S0266-3538(03)00064-2 ↗
25. 10.1016/j.compscitech.2005.10.01910.1016/j.compscitech.2005.10.019 ↗
26. 10.1016/j.compscitech.2006.02.02610.1016/j.compscitech.2006.02.026 ↗
27. 10.1007/s12034-008-0032-210.1007/s12034-008-0032-2 ↗
28. 10.1088/0960-1317/24/11/11500410.1088/0960-1317/24/11/115004 ↗
29. 10.1016/S0924-4247(96)01401-X10.1016/S0924-4247(96)01401-X ↗
30. 10.1109/84.99344810.1109/84.993448 ↗
31. 10.1063/1.114450910.1063/1.1144509 ↗