Binding studies of molecular linkers to ZnO and MgZnO nanotip films

被引:122
作者
Taratula, O
Galoppini, E
Wang, D
Chu, D
Zhang, Z
Chen, HH
Saraf, G
Lu, YC
机构
[1] Rutgers State Univ, Dept Chem, Newark, NJ 07102 USA
[2] Rutgers State Univ, Dept Elect & Comp Engn, Piscataway, NJ 08854 USA
关键词
D O I
10.1021/jp0570317
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two bifunctional linkers, a rigid-rod p-ethynyl-isophthalic acid capped with a Ru(II)-polypyridyl complex and 3-mercaptopropionic acid, were covalently bound to ZnO nanotip films grown by metal-organic chemical vapor deposition (MOCVD) technology. This highly vertically aligned, crystalline form of ZnO had not been functionalized before. The binding was studied by Fourier transform (FT) IR and UV spectroscopies and probed, in the case of the Ru complex, by static and dynamic fluorescence quenching. The molecules did bind through the carboxylic acid groups, and the FT-IR attenuated total reflectance spectra are indicative of a bidentate carboxylate binding mode. Other molecules (heptanoic acid, isophthalic acid, and trimethoxy(2-phenylethyl)silane) were also bound to the ZnO nanotips. A comparison was made with epitaxial ZnO films grown by MOCVD and ZnO mesoporous films prepared from colloidal solutions to investigate the effect of the ZnO morphology. The ZnO nanotips were excellent binding substrates, particularly for the rigid-rod linker. Since ZnO films are etched at low pH (< 4), novel nanotip films made of ternary MgxZn1-xO, which is formed by alloying ZnO with MgO and is more resistant to acids, were developed. The MgxZn1-xO nanotip films were employed to use linkers with acidic groups and to study the effect of pH pretreatment of the surface on the binding.
引用
收藏
页码:6506 / 6515
页数:10
相关论文
共 83 条
[1]   ENHANCED SPECTRAL SENSITIVITY FROM RUTHENIUM(II) POLYPYRIDYL BASED PHOTOVOLTAIC DEVICES [J].
ARGAZZI, R ;
BIGNOZZI, CA ;
HEIMER, TA ;
CASTELLANO, FN ;
MEYER, GJ .
INORGANIC CHEMISTRY, 1994, 33 (25) :5741-5749
[2]   Correlation between structural and electrical properties of ZnO thin films [J].
Asadov, A ;
Gao, W ;
Li, Z ;
Lee, J ;
Hodgson, M .
THIN SOLID FILMS, 2005, 476 (01) :201-205
[3]   Parameters affecting electron injection dynamics from ruthenium dyes to titanium dioxide nanocrystalline thin film [J].
Asbury, JB ;
Anderson, NA ;
Hao, EC ;
Ai, X ;
Lian, TQ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (30) :7376-7386
[4]   Ultrafast electron transfer dynamics from molecular adsorbates to semiconductor nanocrystalline thin films [J].
Asbury, JB ;
Hao, E ;
Wang, YQ ;
Ghosh, HN ;
Lian, TQ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (20) :4545-4557
[5]   Low temperature selective NO2 sensors by nanostructured fibres of ZnO [J].
Baratto, C ;
Sberveglieri, G ;
Onischuk, A ;
Caruso, B ;
di Stasio, S .
SENSORS AND ACTUATORS B-CHEMICAL, 2004, 100 (1-2) :261-265
[6]   Electron injection and recombination in Ru(dcbpy)2(NCS)2 sensitized nanostructured ZnO [J].
Bauer, C ;
Boschloo, G ;
Mukhtar, E ;
Hagfeldt, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (24) :5585-5588
[7]   Ultrafast relaxation dynamics of charge carriers relaxation in ZnO nanocrystalline thin films [J].
Bauer, C ;
Boschloo, G ;
Mukhtar, E ;
Hagfeldt, A .
CHEMICAL PHYSICS LETTERS, 2004, 387 (1-3) :176-181
[8]   Photoinduced electron injection from Ru(dcbPY)2(NCS)2 to SnO2 and TiO2 nanocrystalline films [J].
Benkö, G ;
Myllyperkiö, P ;
Pan, J ;
Yartsev, AP ;
Sundström, V .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (05) :1118-1119
[9]   Photoinduced ultrafast dye-to-semiconductor electron injection from nonthermalized and thermalized donor states [J].
Benkö, G ;
Kallioinen, J ;
Korppi-Tommola, JEI ;
Yartsev, AP ;
Sundström, V .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (03) :489-493
[10]   Properties of ZnO nanotips selectively grown by MOCVD [J].
Chen, HH ;
Zhong, J ;
Saraf, G ;
Zhang, Z ;
Lu, YC ;
Fetter, LA ;
Pai, CS .
NANOFABRICATION: TECHNOLOGIES, DEVICES AND APPLICATIONS, 2004, 5592 :164-169