journal article·2016-11-16

Bioinspired Single-Walled Carbon Nanotubes as a Spider Silk Structure for Ultrahigh Mechanical Property

Chengzhi Luo, Fangying Li, Delong Li, Qiang Fu, Chunxu Pan

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Abstract

Due to its unique hierarchical structure, natural spider silk features exceptional mechanical properties such as high tensile strength and great extensibility, making it one of the toughest materials. Herein, we design bioinspired spider silk single-walled carbon nanotubes (BISS-SWCNTs) that combine the hierarchical structure of spider silk and the high strength and conductivity of SWCNTs. To imitate the hierarchical structure, Fe nanoparticles are embedded on the surface of directly synthesized SWCNTs skeleton followed by coating an amorphous carbon layer. The carbon layer forms the spider silk-featured skin-core structure with SWCNTs, thus making the tube junction tougher. The embedded Fe nanoparticles act as glue spots for preventing interfacial slippages between the BISS-SWCNTs and the reinforced matrix. With only 2.1 wt % BISS-SWCNTs added, the tensile strength and Young's modulus of the BISS-SWCNTs/PMMA composites can be improved by 300%. More importantly, the BISS-SWCNTs also retain the high conductivity and transmittance of the pristine SWCNTs film. This unique bioinspired material will be of great importance in applications of multifunctional composite materials and has important implications for the future of biomimetic materials.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Silk-based biomaterials and applications · Advanced Materials and Mechanics · Electrospun Nanofibers in Biomedical Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Physics and Technology and MOE Key Laboratory of Artificial Micro- and Nano-structures and ‡Center for Electron Microscopy, Wuhan University, Wuhan 430072, China

Funding

National Natural Science Foundation of China

References (34)

Show source-provided references
1. 10.1038/nnano.2014.9310.1038/nnano.2014.93 ↗
2. 10.1021/nn400346r10.1021/nn400346r ↗
3. 10.1021/acsnano.5b0540410.1021/acsnano.5b05404 ↗
4. 10.1038/ncomms432210.1038/ncomms4322 ↗
5. 10.1103/PhysRevLett.84.555210.1103/PhysRevLett.84.5552 ↗
6. 10.1126/science.287.5453.63710.1126/science.287.5453.637 ↗
7. 10.1038/nmat107610.1038/nmat1076 ↗
8. 10.1021/nl901035v10.1021/nl901035v ↗
9. 10.1021/nn400726g10.1021/nn400726g ↗
10. 10.1016/j.carbon.2012.11.03910.1016/j.carbon.2012.11.039 ↗
11. 10.1021/nn502552q10.1021/nn502552q ↗
12. 10.1038/4471066a10.1038/4471066a ↗
13. 10.1021/nl070915c10.1021/nl070915c ↗
14. 10.1021/nn200338r10.1021/nn200338r ↗
15. 10.1038/nature1073910.1038/nature10739 ↗
16. 10.1038/nmat270410.1038/nmat2704 ↗
17. 10.1038/nmat354910.1038/nmat3549 ↗
18. 10.1038/ncomms101910.1038/ncomms1019 ↗
19. 10.1002/adma.20030639310.1002/adma.200306393 ↗
20. 10.1039/C6NR03928F10.1039/C6NR03928F ↗
21. 10.1038/srep0906210.1038/srep09062 ↗
22. 10.1002/adma.20100070510.1002/adma.201000705 ↗
23. 10.1021/acs.nanolett.5b0386310.1021/acs.nanolett.5b03863 ↗
24. 10.1021/nl801271510.1021/nl8012715 ↗
25. 10.1002/adma.20080133510.1002/adma.200801335 ↗
26. 10.1126/science.117124510.1126/science.1171245 ↗
27. 10.1021/jp807380s10.1021/jp807380s ↗
28. 10.1021/nl101680s10.1021/nl101680s ↗
29. 10.1002/adfm.20120101310.1002/adfm.201201013 ↗
30. 10.1021/nl060854310.1021/nl0608543 ↗
31. 10.1021/jacs.5b0373910.1021/jacs.5b03739 ↗
32. 10.1002/adma.20140046310.1002/adma.201400463 ↗
33. 10.1038/nnano.2008.36410.1038/nnano.2008.364 ↗
34. 10.1002/adfm.20090196010.1002/adfm.200901960 ↗