Magnetic field induced quantum dot brightening in liquid crystal synergized magnetic and semiconducting nanoparticle composite assemblies
Source abstract
Abstract
The design and development of multifunctional composite materials from artificial nano-constituents is one of the most compelling current research areas. This drive to improve over nature and produce 'meta-materials' has met with some success, but results have proven limited with regards to both the demonstration of synergistic functionalities and in the ability to manipulate the material properties post-fabrication and in situ. Here, magnetic nanoparticles (MNPs) and semiconducting quantum dots (QDs) are co-assembled in a nematic liquid crystalline (LC) matrix, forming composite structures in which the emission intensity of the quantum dots is systematically and reversibly controlled with a small applied magnetic field (<100 mT). This magnetic field-driven brightening, ranging between a two- to three-fold peak intensity increase, is a truly cooperative effect: the LC phase transition creates the co-assemblies, the clustering of the MNPs produces LC re-orientation at atypical low external field, and this re-arrangement produces compaction of the clusters, resulting in the detection of increased QD emission. These results demonstrate a synergistic, reversible, and an all-optical process to detect magnetic fields and additionally, as the clusters are self-assembled in a fluid medium, they offer the possibility for these sensors to be used in broad ranging fluid-based applications.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Liquid Crystal Research Advancements · Advanced Materials and Mechanics · Pickering emulsions and particle stabilization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Physics
School of Natural Sciences
University of California
Merced CA 95343, USA
References (27)
Show source-provided references
1. Sun · Phys. Rev. Lett. · 2003 · 91 · 16720610.1103/PhysRevLett.91.167206 ↗
2. De · Adv. Mater. · 2008 · 20 · 422510.1002/adma.200703183 ↗
3. Nozik · Chem. Rev. · 2010 · 110 · 687310.1021/cr900289f ↗
4. Claridge · ACS Nano · 2009 · 3 · 24410.1021/nn800820e ↗
5. Okuda · Nanotechnology · 2012 · 23 · 41560110.1088/0957-4484/23/41/415601 ↗
6. Zhang · J. Biomed. Mater. Res., Part A · 2008 · 85A : 3 · 84010.1002/jbm.a.31609 ↗
7. Kim · J. Am. Chem. Soc. · 2005 · 127 · 54410.1021/ja047107x ↗
8. Cruz · J. Phys. Chem. B · 2005 · 109 · 1429210.1021/jp0455024 ↗
9. Ross · Nano Lett. · 2011 · 11 · 259010.1021/nl201516g ↗
10. Roullier · Chem. Mater. · 2008 · 20 · 665710.1021/cm801423r ↗
11. Demortie`re · Small · 2010 · 6 · 134110.1002/smll.201000285 ↗
12. Rodarte · J. Mater. Chem. C · 2013 · 1 · 552710.1039/c3tc31043d ↗
13. Mertelj · Nature · 2013 · 504 · 23710.1038/nature12863 ↗
14. Gardner · Mol. Cryst. Liq. Cryst. · 2011 · 545 · 122710.1080/15421406.2011.571966 ↗
15. Dietl · Nat. Mater. · 2010 · 9 · 96510.1038/nmat2898 ↗
16. Vallooran · Langmuir · 2010 · 29 · 99910.1021/la304563r ↗
17. Salgueiriño-Maceira · Adv. Funct. Mater. · 2006 · 16 · 50910.1002/adfm.200500565 ↗
18. Insin · ACS Nano · 2008 · 2 · 19710.1021/nn700344x ↗
19. Foy · ACS Nano · 2010 · 4 · 521710.1021/nn101427t ↗
20. Berezovsky · Science · 2008 · 320 · 34910.1126/science.1154798 ↗
21. Brochard · J. Phys. · 1970 · 31 · 69110.1051/jphys:01970003107069100 ↗
22. Burylov · J. Magn. Magn. Mater. · 1993 · 122 · 6210.1016/0304-8853(93)91040-E ↗
23. Morozov · Phys. Rev. E: Stat., Nonlinear, Soft Matter Phys. · 2002 · 660 · 1170410.1103/PhysRevE.66.011704 ↗
24. Berejnov · Europhys. Lett. · 1998 · 41 · 50710.1209/epl/i1998-00182-9 ↗
25. Goryca · Phys. Rev. B: Condens. Matter Mater. Phys. · 2010 · 82 · 16532310.1103/PhysRevB.82.165323 ↗
26. Tengood · Proc. Natl. Acad. Sci. U. S. A. · 2014 · 111 · 424510.1073/pnas.1324104111 ↗
27. Sato · Jpn. J. Appl. Phys. · 1981 · 20 · 240310.1143/JJAP.20.2403 ↗