electrochemical surface modification with diazonium salt;
single-crystalline CVD diamond;
covalent DNA attachment;
hybridization reaction;
AFM characterization;
D O I:
10.1016/j.elecom.2006.03.014
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
Electrochemical surface modification via reduction of 4-nitrobenzene diazonium tetrafluoroborate in acetonitrile solution has been performed on highly boron-doped homoepitaxial single-crystalline CVD diamond films to build up surface functionalization for DNA hybridization. Due to significantly improved voltammetric resolution and regularly oriented arrangements, covalently bonded 4-nitrophenyl groups on single-crystalline diamond are characterized to have two successive reversible one-electron transfer reactions interacting with stable radical anion and dianion species. This is new and has not been detected on other electrode materials. Their surface density is in the range of 7.9 x 10(13) molecules/cm(2) or 1.3 x 10(-10) mol/cm(2) as detected by cyclic voltammetric measurements. The aminophenyl-modified diamond surface was further modified by cross linker molecules and thiol-modified DNA oligonucleotides. The resulting DNA immobilization on diamond surface is confirmed by DNA hybridization reaction, using fluorescein-labeled complementary/non-complementary target DNA oligonucleotides. We characterize the DNA film using AFM experiments which reveal a closed and dense film with a height of about 90 angstrom. Finally, we compare the attachment efficiency on initially H-terminated and oxidized diamond surfaces. (c) 2006 Elsevier B.V. All rights reserved.