Network of Inorganic Nanocrystals Can Swell: Study of Swelling‐Induced Surface Instability
Source abstract
Abstract
Abstract A unique organic–inorganic hybrid network composed of inorganic nanocores (ranging from semiconductors to metallic ones) interconnected through organic molecules can be produced by crosslinking the organic ligands of colloidal inorganic nanocrystals in assemblies. This work reports that this network, which is conventionally considered an inorganic film, can swell when exposed to a solvent because of the interaction between the solvent and the organic linkage within the network. Intriguingly, this work discovers that drying the solvent of the swollen organic–inorganic hybrid network can significantly affect the morphology owing to the swelling‐induced compress stress, which is widely observed in various organic network systems. This work studies the surface instability of crosslinked organic–inorganic hybrid networks swollen by various organic solvents, which led to buckling delamination. Specifically, this work investigates the effects of the i) solvent–network interaction, ii) crosslinking density of the network, and iii) thickness of the film on the delamination behavior of the crosslinked network.
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Research context
OpenAlex topics: Advanced Materials and Mechanics · Advanced Sensor and Energy Harvesting Materials · Liquid Crystal Research Advancements
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biomolecular Engineering Sogang University Seoul 04107 South Korea
School of Chemical and Biological Engineering Seoul National University Seoul 08826 South Korea
Institute of Emergent Materials, Ricci Institute of Basic Science Sogang University Seoul 04107 South Korea
Funding
National Research Foundation of Korea · Ministry of Science, ICT and Future Planning · Samsung
References (38)
Show source-provided references
1. 10.1038/srep0888710.1038/srep08887 ↗
2. 10.1039/b516741h10.1039/b516741h ↗
3. 10.1038/3019310.1038/30193 ↗
4. 10.1063/1.155889710.1063/1.1558897 ↗
5. 10.1002/adma.20070153010.1002/adma.200701530 ↗
6. 10.1002/adma.20080320910.1002/adma.200803209 ↗
7. 10.1038/nmat260610.1038/nmat2606 ↗
8. 10.1016/j.actbio.2009.10.02510.1016/j.actbio.2009.10.025 ↗
9. 10.1103/PhysRevLett.90.07430210.1103/PhysRevLett.90.074302 ↗
10. 10.1073/pnas.090991810710.1073/pnas.0909918107 ↗
11. 10.1073/pnas.081044310510.1073/pnas.0810443105 ↗
12. 10.1073/pnas.091122310710.1073/pnas.0911223107 ↗
13. 10.1039/c2sm25859e10.1039/c2sm25859e ↗
14. 10.1002/anie.20140448310.1002/anie.201404483 ↗
15. 10.1039/c2sm25487e10.1039/c2sm25487e ↗
16. 10.1021/nn800853y10.1021/nn800853y ↗
17. 10.1021/la991302l10.1021/la991302l ↗
18. 10.1021/nn305399910.1021/nn3053999 ↗
19. 10.1002/adma.20180541710.1002/adma.201805417 ↗
20. 10.1021/acsami.6b1617510.1021/acsami.6b16175 ↗
21. 10.1021/la901736n10.1021/la901736n ↗
22. 10.1016/j.tsf.2005.11.10610.1016/j.tsf.2005.11.106 ↗
23. 10.1039/b916207k10.1039/b916207k ↗
24. Lin P.‐C. · Appl. Phys. Lett. · 2007 · 90
25. 10.1002/adfm.20090062210.1002/adfm.200900622 ↗
26. 10.1021/am201428m10.1021/am201428m ↗
27. 10.1038/s41467-020-16652-410.1038/s41467-020-16652-4 ↗
28. 10.1002/adma.20220550410.1002/adma.202205504 ↗
29. 10.1002/anie.20220263310.1002/anie.202202633 ↗
30. Shin S. · Small Methods
31. 10.1021/ma300784d10.1021/ma300784d ↗
32. 10.1021/ma400734710.1021/ma4007347 ↗
33. 10.1038/s41565-022-01182-510.1038/s41565-022-01182-5 ↗
34. Park S. Y. · Adv. Mater.
35. 10.1201/978142000683410.1201/9781420006834 ↗
36. 10.1007/s42452-020-2512-y10.1007/s42452-020-2512-y ↗
37. 10.1073/pnas.090216010610.1073/pnas.0902160106 ↗
38. 10.1021/acs.chemmater.9b0074010.1021/acs.chemmater.9b00740 ↗