journal article·2019-02

Directed Self‐Assembly of Templatable Block Copolymers by Easily Accessible Magnetic Control

Bingbing Yue, Xin Jin, Pei Zhao, Mingjie Zhu, Liangliang Zhu

Small· Volume 15· Issue 7
Publisher page

Abstract

Abstract Magnetic control has been a prosperous and powerful contactless approach in arraying materials into high‐order nanostructures. However, it is tremendously difficult to control organic polymers in this way on account of the weak magnetic response. The preparation of block copolymers (BCPs) with high magnetostatic energy is reported here, relying on an effective electrostatic coupling between paramagnetic ions and polymer side chains. As a result, the BCPs undergo a magnetically directed self‐assembly to form microphase‐segregated nanostructures with long‐range order. It is emphasized that such a precisely controlled alignment of the BCPs is performed upon a single commercial magnet with low‐intensity field (0.35 Tesla). This strategy is profoundly easy‐to‐handle in contrast to routine electromagnetic methods with high‐intensity field (5–10 Tesla). More significantly, the paramagnetic metal component in the BCP samples can be smartly removed, providing a template effect with a preservation of the directed self‐assembled nanofeatures for patterning follow‐up functionalized species through the original binding site.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Block Copolymer Self-Assembly · Advanced Polymer Synthesis and Characterization · Nanopore and Nanochannel Transport Studies

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

Affiliations

Key Laboratory of Molecular Engineering of Polymer Department of Macromolecular Science Fudan University Shanghai 200438 China

Shanghai Synchrotron Radiation Facility Chinese Academy of Sciences Shanghai 201204 China

Funding

National Natural Science Foundation of China · China Postdoctoral Science Foundation

References (41)

Show source-provided references
1. 10.1038/nnano.2013.16010.1038/nnano.2013.160 ↗
2. 10.1002/adma.20030490610.1002/adma.200304906 ↗
3. 10.1039/C5SC03505H10.1039/C5SC03505H ↗
4. 10.1002/smll.20120057610.1002/smll.201200576 ↗
5. 10.1002/anie.20130385410.1002/anie.201303854 ↗
6. 10.1021/jacs.5b0332010.1021/jacs.5b03320 ↗
7. 10.1038/s41467-018-05535-410.1038/s41467-018-05535-4 ↗
8. 10.1002/smll.20130380910.1002/smll.201303809 ↗
9. 10.1021/ja507318u10.1021/ja507318u ↗
10. 10.1126/science.aan279710.1126/science.aan2797 ↗
11. 10.1002/adfm.20160299810.1002/adfm.201602998 ↗
12. 10.1002/adma.20110110610.1002/adma.201101106 ↗
13. 10.1002/anie.20080239010.1002/anie.200802390 ↗
14. 10.1038/ncomms148510.1038/ncomms1485 ↗
15. 10.1021/ja311190a10.1021/ja311190a ↗
16. 10.1038/nnano.2010.3010.1038/nnano.2010.30 ↗
17. 10.1002/adma.20120026510.1002/adma.201200265 ↗
18. 10.1002/smll.20157028810.1002/smll.201570288 ↗
19. 10.1021/nl402168310.1021/nl4021683 ↗
20. 10.1038/nnano.2017.3410.1038/nnano.2017.34 ↗
21. 10.1002/smll.20180145210.1002/smll.201801452 ↗
22. 10.1021/ma400325g10.1021/ma400325g ↗
23. 10.1073/pnas.171263111410.1073/pnas.1712631114 ↗
24. 10.1246/cl.2004.159010.1246/cl.2004.1590 ↗
25. 10.1039/c1py00044f10.1039/c1py00044f ↗
26. 10.1039/b515391c10.1039/b515391c ↗
27. 10.1021/ic500882z10.1021/ic500882z ↗
28. 10.1126/sciadv.aar231710.1126/sciadv.aar2317 ↗
29. 10.1002/adma.20170371310.1002/adma.201703713 ↗
30. 10.1039/c2cs35115c10.1039/c2cs35115c ↗
31. 10.1039/C6PY00535G10.1039/C6PY00535G ↗
32. 10.1021/acs.nanolett.5b0146310.1021/acs.nanolett.5b01463 ↗
33. 10.1016/j.surfrep.2009.07.00210.1016/j.surfrep.2009.07.002 ↗
34. 10.1039/c3nr03591c10.1039/c3nr03591c ↗
35. 10.1021/ja309168f10.1021/ja309168f ↗
36. 10.1021/ja050892910.1021/ja0508929 ↗
37. 10.1021/acsami.5b1056210.1021/acsami.5b10562 ↗
38. 10.1002/adfm.20170622610.1002/adfm.201706226 ↗
39. 10.1103/PhysRevB.78.17442210.1103/PhysRevB.78.174422 ↗
40. 10.1021/ma502564m10.1021/ma502564m ↗
41. 10.1007/BF0243733310.1007/BF02437333 ↗