Nanorods Based on Mesoporous Silica Containing Iron Oxide Nanoparticles as Catalytic Nanomotors: Study of Motion Dynamics
Source abstract
Abstract
Abstract Self‐propelled particles and, in particular, those based on mesoporous silica, have raised considerable interest due to their potential applications in the environmental and biomedical fields thanks to their biocompatibility, tunable surface chemistry and large porosity. Although spherical particles have been widely used to fabricate nano‐ and micromotors, not much attention has been paid to other geometries, such as nanorods. Here, we report the fabrication of self‐propelled mesoporous silica nanorods (MSNRs) that move by the catalytic decomposition of hydrogen peroxide by a sputtered Pt layer, Fe2O3 nanoparticles grown within the mesopores, or the synergistic combination of both. We show that motion can occur in two distinct sub‐populations characterized by two different motion dynamics, namely enhanced diffusion or directional propulsion, especially when both catalysts are used. These results open up the possibility of using MSNRs as chassis for the fabrication of self‐propelled particles for the environmental or biomedical fields.
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Research context
OpenAlex topics: Micro and Nano Robotics · Pickering emulsions and particle stabilization · Characterization and Applications of Magnetic Nanoparticles
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Bioengineering of Catalonia (IBEC) The Barcelona Institute of Science and Technology (BIST) Baldiri-Reixac 10–12 08028 Barcelona Spain
Institut de Ciència de Materials de Barcelona (ICMAB-CSIC) Campus UAB 08193 Bellaterra Catalonia Spain
Institució Catalana de Recerca i Estudis Avançats (ICREA) Passeig de Lluís Companys 23 08010 Barcelona Spain
Funding
European Research Council
References (54)
Show source-provided references
1. Sanchez S. · Angew. Chem. Int. Ed. · 2015 · 54 · 141410.1002/anie.201406096 ↗
2. Katuri J. · Acc. Chem. Res. · 2017 · 50 · 210.1021/acs.accounts.6b00386 ↗
3. Popescu M. N. · Acc. Chem. Res. · 2018 · 51 · 299110.1021/acs.accounts.8b00237 ↗
4. Stark H. · Acc. Chem. Res. · 2018 · 51 · 268110.1021/acs.accounts.8b00259 ↗
5. Patiño T. · Acc. Chem. Res. · 2018 · 51 · 266210.1021/acs.accounts.8b00288 ↗
6. Ortiz-Rivera I. · Acc. Chem. Res. · 2018 · 51 · 189110.1021/acs.accounts.8b00199 ↗
7. Wang J. · Acc. Chem. Res. · 2018 · 51 · 195710.1021/acs.accounts.8b00254 ↗
8. Parmar J. · J. Am. Chem. Soc. · 2018 · 140 · 931710.1021/jacs.8b05762 ↗
9. Romanczuk P. · Eur. Phys. J. Spec. Top. · 2012 · 202 · 110.1140/epjst/e2012-01529-y ↗
10. Howse J. R. · Phys. Rev. Lett. · 2007 · 99 · 04810210.1103/PhysRevLett.99.048102 ↗
11. Dey K. K. · Curr. Opin. Colloid Interface Sci. · 2016 · 21 · 410.1016/j.cocis.2015.12.001 ↗
12. Sanchez S. · Angew. Chem. Int. Ed. · 2015 · 54 · 141410.1002/anie.201406096 ↗
13. Paxton W. F. · J. Am. Chem. Soc. · 2004 · 126 · 1342410.1021/ja047697z ↗
14. Wang Y. · Langmuir · 2006 · 22 · 1045110.1021/la0615950 ↗
15. Fournier-Bidoz S. · Chem. Commun. · 2005 · 44110.1039/b414896g ↗
16. Laocharoensuk R. · ACS Nano · 2008 · 2 · 106910.1021/nn800154g ↗
17. Demirok U. K. · Angew. Chem. · 2008 · 120 · 948910.1002/ange.200803841 ↗
18. Mano N. · J. Am. Chem. Soc. · 2005 · 127 · 1157410.1021/ja053937e ↗
19. Pantarotto D. · Chem. Commun. · 2008 · 153310.1039/B715310D ↗
20. Ma X. · J. Am. Chem. Soc. · 2016 · 138 · 1378210.1021/jacs.6b06857 ↗
21. Sanchez S. · J. Am. Chem. Soc. · 2010 · 132 · 1314410.1021/ja104362r ↗
22. Orozco J. · ACS Nano · 2013 · 7 · 81810.1021/nn305372n ↗
23. Solovev A. A. · Small · 2009 · 5 · 168810.1002/smll.200900021 ↗
24. Solovev A. A. · ACS Nano · 2012 · 6 · 175110.1021/nn204762w ↗
25. Magdanz V. · Angew. Chem. Int. Ed. · 2014 · 53 · 267310.1002/anie.201308610 ↗
26. Sanchez S. · Chem. Commun. · 2011 · 47 · 69810.1039/C0CC04126B ↗
27. Solovev A. A. · Adv. Funct. Mater. · 2010 · 20 · 243010.1002/adfm.200902376 ↗
28. Balasubramanian S. · Angew. Chem. Int. Ed. · 2011 · 50 · 416110.1002/anie.201100115 ↗
29. Esteban-Fernández de Ávila B. · Adv. Mater. · 2020 · 32 · 110.1002/adma.202000091 ↗
30. Guix M. · ACS Nano · 2012 · 6 · 444510.1021/nn301175b ↗
31. Soler L. · ACS Nano · 2013 · 7 · 961110.1021/nn405075d ↗
32. Ying Y. · Chem. Eur. J. · 2019 · 25 · 10610.1002/chem.201804189 ↗
33. Campuzano S. · Analyst · 2011 · 136 · 462110.1039/c1an15599g ↗
34. Karshalev E. · J. Am. Chem. Soc. · 2018 · 140 · 381010.1021/jacs.8b00088 ↗
35. García M. · Nanoscale · 2013 · 5 · 132510.1039/C2NR32400H ↗
36. Maria-Hormigos R. · Lab Chip · 2016 · 16 · 239710.1039/C6LC00467A ↗
37. Kong L. · Curr. Opin. Electrochem. · 2018 · 10 · 17410.1016/j.coelec.2018.06.004 ↗
38. Morales-Narváez E. · Small · 2014 · 10 · 254210.1002/smll.201303068 ↗
39. Xuan M. · J. Am. Chem. Soc. · 2016 · 138 · 649210.1021/jacs.6b00902 ↗
40. Ma X. · J. Mater. Sci. Technol. · 2017 · 33 · 106710.1016/j.jmst.2017.06.007 ↗
41. Hortelao A. C. · ACS Nano · 2019 · 13 · 42910.1021/acsnano.8b06610 ↗
42. Ma X. · Chem. Commun. · 2015 · 51 · 546710.1039/C4CC08285K ↗
43. Vilela D. · Nanoscale · 2017 · 9 · 1399010.1039/C7NR04527A ↗
44. Arqué X. · Nat. Commun. · 2019 · 10 · 282610.1038/s41467-019-10726-8 ↗
45. Hortelão A. C. · Adv. Funct. Mater. · 2018 · 28 · 170508610.1002/adfm.201705086 ↗
46. Hortelão A. C. · Adv. Funct. Mater. · 2017 · 1705086 · 1
47. Li J. G. · Small · 2016 · 12 · 598110.1002/smll.201602272 ↗
48. Ma X. · Nano Lett. · 2015 · 15 · 704310.1021/acs.nanolett.5b03100 ↗
49. Golestanian R. · New J. Phys. · 2007 · 9 · 12610.1088/1367-2630/9/5/126 ↗
50. Lardinois O. M. · Biochim. Biophys. Acta Protein Struct. Mol. Enzymol. · 1996 · 1295 · 22210.1016/0167-4838(96)00043-X ↗
51. Ma X. · Nano Lett. · 2015 · 15 · 704310.1021/acs.nanolett.5b03100 ↗
52. Parmar J. · Adv. Funct. Mater. · 2016 · 26 · 415210.1002/adfm.201600381 ↗
53. El-Ghenymy A. · Environ. Sci. Pollut. Res. Int. · 2014 · 21 · 836810.1007/s11356-014-2773-3 ↗
54. Wang X. · J. Colloid Interface Sci. · 2020 · 561 · 79310.1016/j.jcis.2019.11.058 ↗