A facile synthesis of Fe 3 O 4 /nitrogen-doped carbon hybrid nanofibers as a robust peroxidase-like catalyst for the sensitive colorimetric detection of ascorbic acid
Source abstract
Abstract
In recent years, the fabrication of functional nanostructures with multicomponents for a variety of novel biosensors has received considerable attention due to their synergistic improved sensitivity. Herein, we report a facile approach for the preparation of Fe3O4/nitrogen-doped carbon (Fe3O4/N-C) hybrid nanofibers, and construct a sensing platform for the sensitive colorimetric detection of H2O2 and ascorbic acid (AA). During the synthetic process, a discontinuous layer of polypyrrole (PPy) is first polymerized in situ on the surface of the α-Fe2O3 nanofibers under hydrothermal reaction using α-Fe2O3 nanofibers as both a template and an oxidant. Then the prepared α-Fe2O3/PPy nanofibers are converted into Fe3O4/N-C hybrid nanofibers through pyrolysis with a thermochemical reduction process. The resulting Fe3O4/N-C hybrid nanofibers are used as a novel peroxidase mimic towards the oxidation of 3,3,5,5-tetramethylbenzidine (TMB) in the presence of H2O2, with a superior catalytic activity over individual α-Fe2O3 nanofibers, α-Fe2O3/PPy nanofibers, Fe3O4/C nanofibers, and commercial Fe3O4 nanoparticles. Based on the high peroxidase-like activity of Fe3O4/N-C hybrid nanofibers, a sensing platform for the colorimetric detection of AA is developed. A good linear relationship from 0 to 50 μM and a detection limit of 0.04 μM are achieved. This work offers a new method for the preparation of Fe3O4/N-C hybrid nanofibers and presents new potential applications in biosensing, medical diagnostics and environmental monitoring.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advanced Nanomaterials in Catalysis · Electrochemical sensors and biosensors · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Alan G. MacDiarmid Institute
College of Chemistry
Jilin University
Changchun
P. R. China
Institut für Chemie and IRIS Adlershof
Humboldt-Universität zu Berlin
12489 Berlin
Germany
Funding
National Natural Science Foundation of China
References (70)
Show source-provided references
1. Wei · Chem. Soc. Rev. · 2013 · 42 · 606010.1039/c3cs35486e ↗
2. Lin · Acc. Chem. Res. · 2014 · 47 · 109710.1021/ar400250z ↗
3. Ni · Biosens. Bioelectron. · 2014 · 60 · 28610.1016/j.bios.2014.04.029 ↗
4. Zhou · Nanoscale · 2013 · 5 · 158310.1039/c2nr33072e ↗
5. Asati · Angew. Chem., Int. Ed. · 2009 · 48 · 230810.1002/anie.200805279 ↗
6. André · Adv. Funct. Mater. · 2011 · 21 · 50110.1002/adfm.201001302 ↗
7. Nie · J. Mater. Chem. A · 2014 · 2 · 291010.1039/c3ta15051h ↗
8. Yin · J. Mater. Chem. · 2012 · 22 · 52710.1039/C1JM14253D ↗
9. Song · Adv. Mater. · 2010 · 22 · 220610.1002/adma.200903783 ↗
10. Sun · Electrochem. Commun. · 2013 · 26 · 11310.1016/j.elecom.2012.09.032 ↗
11. Zheng · Biosens. Bioelectron. · 2013 · 49 · 51910.1016/j.bios.2013.05.038 ↗
12. Dai · Chem. – Eur. J. · 2009 · 15 · 432110.1002/chem.200802158 ↗
13. He · Nanoscale · 2012 · 4 · 350110.1039/c2nr30310h ↗
14. Wang · Nanoscale · 2011 · 3 · 175610.1039/c0nr00863j ↗
15. Cheng · Analyst · 2016 · 141 · 191810.1039/C5AN02276B ↗
16. Wang · Anal. Bioanal. Chem. · 2016 · 408 · 101510.1007/s00216-015-9219-8 ↗
17. Yuan · ACS Appl. Mater. Interfaces · 2016 · 8 · 985510.1021/acsami.6b00306 ↗
18. Gao · Nat. Nanotechnol. · 2007 · 2 · 57710.1038/nnano.2007.260 ↗
19. Wei · Anal. Chem. · 2008 · 80 · 225010.1021/ac702203f ↗
20. Liu · Chem. – Eur. J. · 2011 · 17 · 62010.1002/chem.201001789 ↗
21. Sun · Adv. Mater. · 2013 · 25 · 13210.1002/adma.201203218 ↗
22. Dong · Nanoscale · 2012 · 4 · 396910.1039/c2nr12109c ↗
23. Wang · RSC Adv. · 2014 · 4 · 4580910.1039/C4RA07327D ↗
24. Shi · Nanoscale · 2016 · 8 · 1081410.1039/C6NR02725C ↗
25. Gong · Science · 2009 · 323 · 76010.1126/science.1168049 ↗
26. Paraknowitsch · Energy Environ. Sci. · 2013 · 6 · 283910.1039/c3ee41444b ↗
27. Zhao · J. Am. Chem. Soc. · 2013 · 135 · 120110.1021/ja310566z ↗
28. Deng · J. Mater. Chem. A · 2016 · 4 · 114410.1039/C5TA08620E ↗
29. Wang · ACS Catal. · 2012 · 2 · 78110.1021/cs200652y ↗
30. Masa · Angew. Chem., Int. Ed. · 2015 · 54 · 1010210.1002/anie.201500569 ↗
31. Jiang · Anal. Chem. · 2017 · 89 · 452510.1021/acs.analchem.6b04949 ↗
32. Jiang · ACS Appl. Mater. Interfaces · 2015 · 7 · 309310.1021/am507163z ↗
33. Jiang · Biosens. Bioelectron. · 2014 · 54 · 27310.1016/j.bios.2013.11.005 ↗
34. Jiang · Carbon · 2016 · 102 · 1010.1016/j.carbon.2016.02.027 ↗
35. Yang · Biosens. Bioelectron. · 2015 · 65 · 3910.1016/j.bios.2014.10.004 ↗
36. Zhou · J. Mater. Chem. B · 2016 · 4 · 624910.1039/C6TB01414C ↗
37. Li · Catal. Sci. Technol. · 2016 · 6 · 367010.1039/C6CY00544F ↗
38. Chang · Chem. – Asian J. · 2016 · 11 · 112510.1002/asia.201501328 ↗
39. Shi · Sens. Actuators, B · 2015 · 221 · 151510.1016/j.snb.2015.06.157 ↗
40. Shen · J. Mater. Chem. A · 2015 · 3 · 1311410.1039/C5TA01228G ↗
41. Suma · ACS Sustainable Chem. Eng. · 2015 · 3 · 13310.1021/sc500629p ↗
42. Ma · Eur. J. Inorg. Chem. · 2016 · 372210.1002/ejic.201600432 ↗
43. Lei · Nanoscale · 2013 · 5 · 116810.1039/c2nr33043a ↗
44. Pinna · Chem. Mater. · 2005 · 17 · 304410.1021/cm050060+ ↗
45. Lin · Electrochim. Acta · 2016 · 216 · 28710.1016/j.electacta.2016.09.033 ↗
46. Bose · Polymer · 2010 · 51 · 592110.1016/j.polymer.2010.10.014 ↗
47. Faria · J. Raman Spectrosc. · 1997 · 28 · 87310.1002/(SICI)1097-4555(199711)28:11<873::AID-JRS177>3.0.CO;2-B ↗
48. Kaczmarczyk · ACS Catal. · 2016 · 6 · 123510.1021/acscatal.5b02642 ↗
49. Lim · Synth. Met. · 1999 · 106 · 110.1016/S0379-6779(99)00112-5 ↗
50. Lu · Polym. Compos. · 2009 · 30 · 84710.1002/pc.20666 ↗
51. Cheng · CrystEngComm · 2011 · 13 · 226810.1039/c0ce00802h ↗
52. Liu · J. Colloid Interface Sci. · 2017 · 490 · 67710.1016/j.jcis.2016.11.099 ↗
53. Nasibulin · Nano Res. · 2009 · 2 · 37310.1007/s12274-009-9036-5 ↗
54. Jia · Appl. Surf. Sci. · 2012 · 258 · 662710.1016/j.apsusc.2012.03.092 ↗
55. Zhao · Chem. Commun. · 2013 · 49 · 765610.1039/c3cc43154a ↗
56. Chi · ACS Appl. Mater. Interfaces · 2016 · 8 · 104110.1021/acsami.5b11488 ↗
57. Nie · Dalton Trans. · 2013 · 284 · 595
58. Notsu · J. Electroanal. Chem. · 2002 · 523 · 8610.1016/S0022-0728(02)00733-7 ↗
59. Zhang · J. Mater. Chem. B · 2015 · 3 · 414610.1039/C5TB00413F ↗
60. Meister · Biochem. Pharmacol. · 1992 · 44 · 190510.1016/0006-2952(92)90091-V ↗
61. Ai · Chem. – Eur. J. · 2013 · 19 · 1510510.1002/chem.201303051 ↗
62. Gao · Nat. Nanotechnol. · 2007 · 2 · 57710.1038/nnano.2007.260 ↗
63. Song · Adv. Mater. · 2011 · 23 · 421510.1002/adma.201101853 ↗
64. Zhang · Chem. Commun. · 2014 · 50 · 109210.1039/C3CC48398C ↗
65. Tan · Chem. – Eur. J. · 2014 · 20 · 1637710.1002/chem.201404960 ↗
66. Chen · Microchim. Acta · 2016 · 183 · 184710.1007/s00604-016-1826-3 ↗
67. Peng · Sens. Actuators, B · 2015 · 221 · 70810.1016/j.snb.2015.07.002 ↗
68. Wu · Anal. Chem. · 2006 · 78 · 557010.1021/ac0603577 ↗
69. Fan · Biosens. Bioelectron. · 2017 · 89 · 84610.1016/j.bios.2016.09.108 ↗
70. Darabdhara · Sens. Actuators, B · 2017 · 238 · 84210.1016/j.snb.2016.07.106 ↗