Liquid crystalline nanoconfined growth of PANI on rGO for enhanced electrochemical glucose sensing
Source abstract
Abstract
We report here a new strategy for the successful synthesis of a hybrid 2D nanocomposite via the in situ functionalization of graphene oxide (GO) with aniline monomers in a bi-solvent swollen liquid crystalline lamellar mesophase (SLCLM) nanoreactor. The synthesized nanocomposite product revealed possible simultaneous reactions at the edge and basal plane of GO. A mechanism for the transformation via simultaneous nucleophilic attack and spontaneous polymerization, forming a reduced graphene oxide-polyaniline (rGO-PANI) nanocomposite, is proposed. The multistep plausible reaction mechanism for the functionalization of the GO edge -COOH group is achieved by successful synthesis, followed by isolation and characterization of the N-phenyl anthranilic acid derivative as an intermediate product. Furthermore, the detection of CO2 evolution as a by-product during the reaction complements the plausible mechanism for the incorporation of (-CC-) graphyne-type edges and formation of new -C-N- and O-H bonds in the rGO-PANI nanocomposite. These results are supported by FT-IR, Raman, XPS, SAXS, and 13C NMR spectroscopy analyses. A reduced graphene oxide-polyaniline (rGO-PANI) modified glassy carbon electrode was developed for glucose sensing, exhibiting a wide linear range (0.554-10 µM), low detection limit (50 pM), and high sensitivity (372 660 µA mM-1 cm-2). The sensor demonstrated excellent selectivity against common interferents (ascorbic acid, uric acid, and dopamine), reproducibility (RSD < 5%), and stability over 10 000 s with minimal signal loss. The detection of glucose from human metabolites, such as urine and sweat, achieved 98-100% recoveries for spiked glucose, confirming its practical applicability. These results establish rGO-PANI as a robust platform for sensitive and selective glucose detection.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Electrochemical sensors and biosensors · Conducting polymers and applications · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Nanoscience and Biotechnology, Shivaji University, Kolhapur 416004, Maharashtra, India
Science Division, New York University, Saadiyat Island, Abu Dhabi-129188, United Arab Emirates
Department of Chemistry, Shivaji University, Kolhapur 416004, Maharashtra, India
Department of Chemistry, SavitribaiPhule Pune University, Pune 411007, Maharashtra, India
Chemical Engineering and Process Development (CEPD) Division, CSIR-National Chemical Laboratory (NCL), Pune 411008, Maharashtra, India
References (44)
Show source-provided references
1. Pappa · Biotechnology · 2018 · 36 · 45
2. Gifford · ChemPhysChem · 2013 · 14 · 203210.1002/cphc.201300172 ↗
3. WitkowskaNery · Anal. Chem. · 2016 · 88 · 1127110.1021/acs.analchem.6b03151 ↗
4. Anupriya · Composites, Part B · 2022 · 242 · 11007910.1016/j.compositesb.2022.110079 ↗
5. Babulal · Composites, Part B · 2022 · 237 · 10984710.1016/j.compositesb.2022.109847 ↗
6. Sun · Talanta · 2021 · 225 · 12207210.1016/j.talanta.2020.122072 ↗
7. Liu · Colloids Surf. · 2023 · 677 · 13241910.1016/j.colsurfa.2023.132419 ↗
8. Shi · Anal. Chem. · 2023 · 95 · 1451610.1021/acs.analchem.3c03702 ↗
9. Liu · J. Colloid Interface Sci. · 2024 · 671 · 42310.1016/j.jcis.2024.05.195 ↗
10. Brezesinski · J. Am. Chem. Soc. · 2009 · 131 · 180210.1021/ja8057309 ↗
11. Kahlouche · Talanta · 2018 · 178 · 43210.1016/j.talanta.2017.09.065 ↗
12. Wang · Sens. Actuators, B · 2015 · 211 · 33210.1016/j.snb.2015.01.056 ↗
13. Hu · Electrochim. Acta · 2009 · 54 · 405610.1016/j.electacta.2009.02.032 ↗
14. Xie · Chin. Chem. Lett. · 2021 · 32 · 206110.1016/j.cclet.2020.10.001 ↗
15. Vadivel · Ceram. Int. · 2024 · 50 · 4465910.1016/j.ceramint.2024.08.313 ↗
16. Venkatesh · J. Ind. Eng. Chem. · 2022 · 106 · 28710.1016/j.jiec.2021.11.005 ↗
17. Karthika · Ultrason. Sonochem. · 2019 · 55 · 19610.1016/j.ultsonch.2019.01.038 ↗
18. Guo · Angew. Chem., Int. Ed. · 2020 · 59 · 154210.1002/anie.201913461 ↗
19. Chua · ACS Nano · 2015 · 9 · 419310.1021/acsnano.5b00438 ↗
20. Iwase · J. Am. Chem. Soc. · 2016 · 138 · 1026010.1021/jacs.6b05304 ↗
21. Qian · Angew. Chem. · 2012 · 124 · 1072210.1002/ange.201206107 ↗
22. Bonaccorso · Nat. Photonics · 2010 · 4 · 61110.1038/nphoton.2010.186 ↗
23. Raccichini · Nat. Mater. · 2015 · 14 · 27110.1038/nmat4170 ↗
24. Loh · Nat. Chem. · 2010 · 2 · 101510.1038/nchem.907 ↗
25. Hung · Chem. Mater. · 2014 · 26 · 298310.1021/cm5007873 ↗
26. Tawade · Chem. Eng. J. · 2024 · 492 · 15184310.1016/j.cej.2024.151843 ↗
27. Khan · J. Mater. Chem. A · 2015 · 3 · 1875310.1039/C5TA02240A ↗
28. Yang · Nat. Mater. · 2017 · 16 · 119810.1038/nmat5025 ↗
29. Agyeman · Adv. Energy Mater. · 2016 · 6 · 160090410.1002/aenm.201600904 ↗
30. Li · J. Am. Chem. Soc. · 2011 · 133 · 1087810.1021/ja2025454 ↗
31. Marcano · ACS Nano · 2010 · 4 · 480610.1021/nn1006368 ↗
32. Lou · Adv. Mater. · 2008 · 20 · 398710.1002/adma.200800854 ↗
33. Chang · Energy Environ. Sci. · 2013 · 6 · 348310.1039/c3ee42518e ↗
34. Minewaki · Langmuir · 2001 · 17 · 186410.1021/la000791i ↗
35. Mehta · J. Mol. Liq. · 2021 · 326 · 11530210.1016/j.molliq.2021.115302 ↗
36. Li · J. Am. Chem. Soc. · 2018 · 140 · 496910.1021/jacs.7b13247 ↗
37. Karuppasamy · Electrocatalysis · 2022 · 13 · 26910.1007/s12678-022-00707-9 ↗
38. Kumar · J. Catal. · 2023 · 34110.1016/j.jcat.2022.12.019 ↗
39. Kumar · Inorg. Chem. · 2021 · 61 · 27910.1021/acs.inorgchem.1c02819 ↗
40. Surendran · Chem. Mater. · 2005 · 17 · 150510.1021/cm0484495 ↗
41. Kamble · J. Mol. Liq. · 2021 · 324 · 11511910.1016/j.molliq.2020.115119 ↗
42. A. J.Bard , L. R.Faulkner and H. S.White , Electrochemical Methods: Fundamentals and Applications , 3rd ed., John Wiley & Sons , 2022
43. Aljabali · Dalton Trans. · 2010 · 39 · 756910.1039/c0dt00495b ↗
44. Kumar · ACS Nano · 2012 · 6 · 171510.1021/nn204688c ↗