TiO2@CeOx Core–Shell Nanoparticles as Artificial Enzymes with Peroxidase-Like Activity
Source abstract
Abstract
The Ce4+↔Ce3+ redox switch is at the basis of an all-inorganic catalytic cycle that is capable of mimicking the activity of several natural redox enzymes. The efficiency of these artificial enzymes (nanozymes) strongly depends on the Ce4+/Ce3+ ratio. By capitalizing on the results obtained on oxide/oxide model systems, we implemented a simple and effective procedure to obtain conformal TiO2@CeOx core-shell nanoparticles whose thickness is controlled with single-layer precision. Since the Ce3+ species are stabilized only at the interface by the electronic hybridization with the TiO2 states, the modulation of the shell thickness offers a simple method to tailor the Ce4+/Ce3+ ratio and therefore the catalytic properties. The activity of these nanoparticles as artificial peroxidase-like enzymes was tested, showing exceptional performances, even better than natural horseradish peroxidase enzyme. The main advantage with respect to other oxide/oxide nanozymes is that our nanoparticles, having a tunable Ce4+/Ce3+ ratio, are efficient already at low H2O2 concentrations.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Nanomaterials in Catalysis · Nanocluster Synthesis and Applications · Electrochemical sensors and biosensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Sciences, University of Padova, via Marzolo 1, I-35131 Padova, Italy
Department of Chemistry, University of Torino, via Giuria 7, 10125 Torino, Italy
Funding
Ministero dell'Istruzione, dell'Università e della Ricerca
References (49)
Show source-provided references
1. Senanayake S. D. · Acc. Chem. Res. · 2013 · 46 · 170210.1021/ar300231p ↗
2. Rodriguez J. A. · Angew. Chem., Int. Ed. · 2009 · 48 · 804710.1002/anie.200903918 ↗
3. Fu Q. · Science · 2003 · 301 · 93510.1126/science.1085721 ↗
4. Bunluesin T. · Appl. Catal., B · 1998 · 15 · 10710.1016/S0926-3373(97)00040-4 ↗
5. Li H. · ACS Appl. Mater. Interfaces · 2010 · 2 · 83810.1021/am900829y ↗
6. Rao G. R. · J. Catal. · 1996 · 162 · 110.1006/jcat.1996.0254 ↗
7. Esch F. · Science · 2005 · 309 · 75210.1126/science.1111568 ↗
8. Campbell C. T. · Science · 2005 · 309 · 71310.1126/science.1113955 ↗
9. Karakoti A. S. · J. Am. Chem. Soc. · 2009 · 131 · 1414410.1021/ja9051087 ↗
10. Pirmohamed T. · Chem. Commun. · 2010 · 46 · 273610.1039/b922024k ↗
11. Korsvik C. · Chem. Commun. · 2007 · 46 · 105610.1039/b615134e ↗
12. Chen J. P. · Nat. Nanotechnol. · 2006 · 1 · 14210.1038/nnano.2006.91 ↗
13. Asati A. · Angew. Chem., Int. Ed. · 2009 · 48 · 230810.1002/anie.200805279 ↗
14. Hirst S. M. · Small · 2009 · 5 · 284810.1002/smll.200901048 ↗
15. Menchón C. · Small · 2008 · 8 · 189510.1002/smll.201102255 ↗
16. Pinna A. · ACS Appl. Mater. Interfaces · 2013 · 5 · 316810.1021/am4001024 ↗
17. Sayle T. X. T. · Chem. Commun. · 2004 · 243810.1039/b408752f ↗
18. Deshpande S. · Appl. Phys. Lett. · 2005 · 87 · 13311310.1063/1.2061873 ↗
19. Cargnello M. · Science · 2012 · 337 · 71310.1126/science.1222887 ↗
20. Zhou G. · Angew. Chem., Int. Ed. · 2010 · 49 · 968010.1002/anie.201004966 ↗
21. Gionco C. · J. Mater. Chem. A · 2013 · 1 · 1091810.1039/c3ta12018j ↗
22. Chen L. · ACS Appl. Mater. Interfaces · 2014 · 6 · 813410.1021/am5004969 ↗
23. Graciani J. · J. Chem. Phys. · 2010 · 132 · 10470310.1063/1.3337918 ↗
24. Agnoli S. · Nanoscale · 2014 · 6 · 80010.1039/C3NR04623K ↗
25. Park J. B. · Proc. Natl. Acad. Sci. U. S. A. · 2009 · 106 · 497510.1073/pnas.0812604106 ↗
26. Abbott H. L. · J. Catal. · 2010 · 272 · 8210.1016/j.jcat.2010.03.009 ↗
27. Wei S. · Nanoscale · 2011 · 3 · 447410.1039/c1nr11000d ↗
28. Gao J. · Acc. Chem. Res. · 2009 · 42 · 109710.1021/ar9000026 ↗
29. Correa D. N. · J. Phys. Chem. C · 2011 · 115 · 1038010.1021/jp200540g ↗
30. Sutara F. · Thin Solid Films · 2008 · 516 · 612010.1016/j.tsf.2007.11.013 ↗
31. Reddy B. M. · J. Phys. Chem. B · 2003 · 107 · 1147510.1021/jp0358376 ↗
32. Yakovlev V. V. · Appl. Phys. Lett. · 2000 · 76 · 110710.1063/1.125953 ↗
33. Lin J. · J. Photochem. Photobiol., A · 1998 · 116 · 6310.1016/S1010-6030(98)00289-5 ↗
34. Hadjiivanov K. I. · Chem. Soc. Rev. · 1996 · 25 · 6110.1039/cs9962500061 ↗
35. Martos M. · Eur. J. Inorg. Chem. · 2008 · 316310.1002/ejic.200800303 ↗
36. Manea F. · Angew. Chem., Int. Ed. · 2004 · 43 · 616510.1002/anie.200460649 ↗
37. Heckert E. G. · Biomaterials · 2008 · 29 · 270510.1016/j.biomaterials.2008.03.014 ↗
38. Peng Y. F. · Chem. Commun. · 2011 · 47 · 291610.1039/c0cc04679e ↗
39. Gao L. Z. · Nat. Nanotechnol. · 2007 · 2 · 57710.1038/nnano.2007.260 ↗
40. Chen W. · ChemCatChem · 2011 · 3 · 115110.1002/cctc.201100064 ↗
41. Dai Z. H. · Chem.—Eur. J. · 2009 · 15 · 432110.1002/chem.200802158 ↗
42. Dutta A. K. · ACS Appl. Mater. Interfaces · 2012 · 4 · 191910.1021/am300408r ↗
43. Song Y. J. · Adv. Mater. · 2010 · 22 · 220610.1002/adma.200903783 ↗
44. Reeder A. E. · J. Phys. Chem. C · 2014 · 118 · 802610.1021/jp500759h ↗
45. Artiglia L. · J. Am. Chem. Soc. · 2013 · 135 · 1733110.1021/ja404889v ↗
46. Ganduglia-Pirovano M. V. · J. Am. Chem. Soc. · 2010 · 132 · 234510.1021/ja910574h ↗
47. Artiglia L. · ACS Catal. · 2014 · 4 · 371510.1021/cs5008798 ↗
48. Chen J. · J. Phys. Chem. C · 2008 · 112 · 130810.1021/jp711191j ↗
49. Lin J.-L. · ACS Catal. · 2013 · 3 · 56010.1021/cs300766d ↗