Facile Method for Modification of the Silicon Nanowires and Its Application in Fabrication of pH-Sensitive Chips
Source abstract
Abstract
A novel, facile, and effective method for modification of SiNWs or SiNW arrays has been developed. In this method, reaction between reductive Si-H bonds on the surface of SiNWs and the aldehyde group containing in organic molecules has been used for immobilization of organic molecules onto the surface of SiNW arrays. The method is time saving and can be operated at room temperature without any other complex reaction requirement. Fluorescence images, XPS, fluorescence spectra, and IR spectra were used for characterization of the modification. Through this method, a SiNW array-based pH sensitive chip was realized by covalently immobilizing 5-aminofluorescein molecules onto the surface of SiNW arrays with glutaraldehyde as linker molecules. Fluorescence intensity of the chip increased with increasing of pH value and a linear relationship between fluorescence intensity and pH values was acquired. In addition, the chip has been successfully used for real-time and in situ monitoring of extracellular pH changes for live HeLa cells and the result exhibited fine resolution of time and space.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanowire Synthesis and Applications · Molecular Junctions and Nanostructures · Semiconductor materials and devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190 China
Graduate School of Chinese Academy of Sciences, Beijing, 100039 China
References (37)
Show source-provided references
1. Cui Y. · Science · 2001 · 291 · 85110.1126/science.291.5505.851 ↗
2. Michael T. K. · Nature · 1996 · 382 · 214
3. Shao M. W. · Adv. Funct. Mater. · 2005 · 15 · 147810.1002/adfm.200500080 ↗
4. Gao Z. Q. · Anal. Chem. · 2007 · 79 · 329110.1021/ac061808q ↗
5. Li Z. · Nano Lett. · 2004 · 4 · 24510.1021/nl034958e ↗
6. Hahm J. · Nano Lett. · 2004 · 4 · 5110.1021/nl034853b ↗
7. Masood M. N. · ACS Appl. Mater. Interfaces · 2010 · 2 · 342210.1021/am100922e ↗
8. Assad O. · J. Am. Chem. Soc. · 2008 · 130 · 1767010.1021/ja807888k ↗
9. Paska Y. · ACS Appl. Mater. Inter. · 2012 · 4 · 260410.1021/am300288z ↗
10. Rabah B. · J. Am. Chem. Soc. · 1999 · 121 · 1151310.1021/ja992032w ↗
11. Yang M.-L. · Langmuir · 2008 · 24 · 793110.1021/la800462u ↗
12. Aswal D. K. · Anal. Chim. Acta · 2006 · 568 · 8410.1016/j.aca.2005.10.027 ↗
13. Jillian M. B. · Chem. Rev. · 2002 · 102 · 1272
14. Fan H. Y. · Nature · 2000 · 405 · 5610.1038/35011026 ↗
15. Miao R. · J. Mater. Chem. · 2012 · 22 · 334810.1039/c1jm15165g ↗
16. Nesrine A. · Langmuir · 2012 · 28 · 65610.1021/la2036778 ↗
17. Yang C. S. · J. Am. Chem. Soc. · 1999 · 121 · 519110.1021/ja9828509 ↗
18. Christian S. · Small · 2012 · 8 · 56910.1002/smll.201101822 ↗
19. Matthew R. L. · J. Am. Chem. Soc. · 1995 · 117 · 314510.1021/ja00116a019 ↗
20. Rabah B. · J. Am. Chem. Soc. · 1999 · 121 · 1151310.1021/ja992032w ↗
21. Su Y. Y. · Nano Lett. · 2012 · 12 · 184510.1021/nl204203t ↗
22. Puniredd S. R. · Langmuir · 2011 · 27 · 476410.1021/la2002546 ↗
23. Paska Y. · ACS Nano · 2011 · 5 · 562010.1021/nn201184c ↗
24. Bashouti M. Y. · Small · 2009 · 5 · 276110.1002/smll.200901402 ↗
25. Hacker C. A. · Langmuir · 2005 · 21 · 88210.1021/la048841x ↗
26. He Y. · Angew. Chem. · 2009 · 121 · 13410.1002/ange.200802230 ↗
27. He Y. · Angew. Chem. · 2011 · 123 · 313610.1002/ange.201100482 ↗
28. Elisabeth G. · ACS Appl. Mater. Inter. · 2009 · 1 · 139610.1021/am900087s ↗
29. Peng K. Q. · Nano Lett. · 2009 · 9 · 370410.1021/nl901734e ↗
30. Ingrid K. H. · Starch · 2006 · 58 · 61610.1002/star.200600546 ↗
31. Wu J. S. · Org. Lett. · 2007 · 9 · 3310.1021/ol062518z ↗
32. George J. C. · Appl. Phys. Lett. · 1985 · 47 · 60410.1063/1.96086 ↗
33. Wagner C. D. · J. Vac. Sci. Technol. · 1982 · 21 · 93310.1116/1.571870 ↗
34. Han Z. Y. · J. Am. Chem. Soc. · 2012 · 134 · 653210.1021/ja3007148 ↗
35. Vikram P. D. · ACS Appl. Mater. Interfaces · 2011 · 3 · 283010.1021/am200324f ↗
36. Izumi H. · Cancer Treatment Rev. · 2003 · 29 · 54110.1016/S0305-7372(03)00106-3 ↗
37. Xu T. · Landes Biosci. · 2011 · 11 · 1316