Facile one-pot synthesis of folic acid-modified graphene to improve the performance of graphene-based sensing strategy

Journal of Colloid and Interface Science

Volumn 426, Issue , 2014, Pages 293-299

  Zhan, Lei ^a   Zhang, Yan ^a   Zeng, Qiao Ling ^a   Liu, Zhong De ^a   Huang, Cheng Zhi ^a  

^a SOUTHWEST UNIVERSITY   (China)

Author keywords

Folic acid; Graphene based sensing strategy; Reduced graphene oxide

Indexed keywords

BIOCOMPATIBILITY; ENERGY TRANSFER; FOURIER TRANSFORM INFRARED SPECTROSCOPY; FUNCTIONAL GROUPS; ORGANIC ACIDS; THERMOGRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; ULTRAVIOLET SPECTROSCOPY; X RAY DIFFRACTION;

FOLIC ACIDS; FOURIER TRANSFORM INFRA RED (FTIR) SPECTROSCOPY; GRAPHENE-BASED SENSING STRATEGY; OXYGEN-CONTAINING FUNCTIONAL GROUPS; PEROXIDASE-LIKE ACTIVITIES; REDUCED GRAPHENE OXIDES; REDUCED GRAPHENE OXIDES (RGO); UV-VIS ABSORPTION SPECTROSCOPY;

GRAPHENE;

FOLIC ACID; GRAPHENE; GRAPHENE OXIDE; HYDROGEN PEROXIDE; OXYGEN; PEROXIDASE; TETRAMETHYLBENZIDINE; GRAPHITE;

ABSORPTION SPECTROSCOPY; ARTICLE; BIOCOMPATIBILITY; COLORIMETRY; ENERGY TRANSFER; INFRARED SPECTROSCOPY; ONE POT SYNTHESIS; OXIDATION; PRIORITY JOURNAL; RAMAN SPECTROMETRY; TASK PERFORMANCE; THERMOGRAVIMETRY; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION; CHEMISTRY; ULTRAVIOLET SPECTROPHOTOMETRY;

FOLIC ACID; GRAPHITE; HYDROGEN PEROXIDE; MICROSCOPY, ELECTRON, TRANSMISSION; SPECTROPHOTOMETRY, ULTRAVIOLET; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; THERMOGRAVIMETRY; X-RAY DIFFRACTION;

EID: 84899796749     PISSN: 00219797     EISSN: 10957103     Source Type: Journal    
DOI: 10.1016/j.jcis.2014.03.056     Document Type: Article

References (37)

1. Rao C.N.R., Sood A.K., Subrahmanyam K.S., Govindaraj A. Angew. Chem. Int. Ed. 2009, 48:7752.
2. He Q., Wu S., Yin Z., Zhang H. Chem. Sci. 2012, 3:1764.
3. Li N., Cao M., Hu C. Nanoscale 2012, 4:6205.
4. Liu Y., Dong X., Chen P. Chem. Soc. Rev. 2012, 41:2283.
5. Novoselov K.S., Geim A.K., Morozov S.V., Jiang D., Zhang Y., Dubonos S.V., Grigorieva I.V., Firsov A.A. Science 2004, 306:666.
6. Park S., An J., Piner R.D., Jung I., Yang D., Velamakanni A., Nguyen S.T., Ruoff R.S. Chem. Mater. 2008, 20:6592.
7. Berger C., Song Z., Li T., Li X., Ogbazghi A.Y., Feng R., Dai Z., Marchenkov A.N., Conrad E.H., First P.N., de Heer W.A. J. Phys. Chem. B 2004, 108:19912.
8. Tung V.C., Allen M.J., Yang Y., Kaner R.B. Nat. Nanotechnol. 2009, 4:25.
9. Zhang J., Yang H., Shen G., Cheng P., Zhang J., Guo S. Chem. Commun. 2010, 46:1112.
10. Zhu C., Guo S., Fang Y., Dong S. ACS Nano 2010, 4:2429.
11. Pham T.A., Kim J.S., Kim J.S., Jeong Y.T. Colloids Surf., A 2011, 384:543.
12. Zhang Z., Chen H., Xing C., Guo M., Xu F., Wang X., Gruber H.J., Zhang B., Tang J. Nano Res. 2011, 4:599.
13. Wang Y., Zhang P., Liu C.F., Zhan L., Li Y.F., Huang C.Z. RSC Adv. 2012, 2:2322.
14. Liu J., Fu S., Yuan B., Li Y., Deng Z. J. Am. Chem. Soc. 2010, 132:7279.
15. Low P.S., Henne W.A., Doorneweerd D.D. Acc. Chem. Res. 2008, 41:120.
16. Zhang L., Xia J., Zhao Q., Liu L., Zhang Z. Small 2010, 6:537.
17. Huang P., Xu C., Lin J., Wang C., Wang X., Zhang C., Zhou X., Guo S., Cui D. Theranostics 2011, 1:240.
18. Waters A.H., Mollin D.L., Pope J., Towler T. J. Clin. Pathol. 1961, 14:335.
19. Hummers W.S., Offerman R.E. J. Am. Chem. Soc. 1958, 80:1339.
20. Li G., Li D., Zhang L., Zhai J., Wang E. Chem. Eur. J. 2009, 15:9868.
21. Luo Z.T., Lu Y., Somers L.A., Johnson A.T.C. J. Am. Chem. Soc. 2009, 131:898.
22. Li D., Müller M.B., Gilje S., Kaner R.B., Wallace G.G. Nat. Nanotechnol. 2008, 3:101.
23. Ouyang H., Wang L., Tian J., Liang A., Jiang Z. Food Anal. Methods 2013, 6:76.
24. Fan X., Peng W., Li Y., Li X., Wang S., Zhang G., Zhang F. Adv. Mater. 2008, 20:4490.
25. Shao Y., Wang J., Engelhard M., Wang C., Lin Y. J. Mater. Chem. 2010, 20:743.
26. Guo H.-L., Wang X.-F., Qian Q.-Y., Wang F.-B., Xia X.-H. ACS Nano 2009, 3:2653.
27. Cao H., Wu X., Yin G., Warner J.H. Inorg. Chem. 2012, 51:2954.
28. Stankovich S., Dikin D.A., Piner R.D., Kohlhaas K.A., Kleinhammes A., Jia Y., Wu Y., Nguyen S.T., Ruoff R.S. Carbon 2007, 45:1558.
29. Hassan H.M.A., Abdelsayed V., Khder A.E.R.S., AbouZeid K.M., Terner J., El-Shall M.S., Al-Resayes S.I., El-Azhary A.A. J. Mater. Chem. 2009, 19:3832.
30. Bose S., Drzal L.T. Nanotechnology 2014, 25:075702. (9pp).
31. Wu Z.-S., Ren W., Gao L., Zhao J., Chen Z., Liu B., Tang D., Yu B., Jiang C., Cheng H.-M. ACS Nano 2009, 3:411.
32. Hussain S.M., Braydich-Stolle L.K., Schrand A.M., Murdock R.C., Yu K.O., Mattie D.M., Schlager J.J., Terrones M. Adv. Mater. 2009, 21:1549.
33. Sapsford K.E., Berti L., Medintz I.L. Angew. Chem. Int. Ed. 2006, 45:4562.
34. Swathi R.S., Sebastian K.L. J. Chem. Sci. 2009, 21:777.
35. Swathi R.S., Sebastian K.L. J. Chem. Phys. 2009, 130:086101.
36. Kim J., Cote L.J., Kim F., Huang J. J. Am. Chem. Soc. 2010, 132:260.
37. Wei H., Wang E. Chem. Soc. Rev. 2013, 42:6060.