Enhancing photoluminescence quenching and photoelectric properties of CdSe quantum dots with hole accepting ligands

被引:231
作者
Liu, I-Shuo [2 ]
Lo, Hsi-Hsing [2 ]
Chien, Chih-Tao [2 ]
Lin, Yun-Yue [2 ]
Chen, Chun-Wei [2 ]
Chen, Yang-Fang [1 ]
Su, Wei-Fang [2 ]
Liou, Sz-Chian [3 ]
机构
[1] Natl Taiwan Univ, Dept Phys, Taipei 10764, Taiwan
[2] Natl Taiwan Univ, Dept Mat & Engn, Taipei 10764, Taiwan
[3] Natl Taiwan Univ, Ctr Condensed Matter Sci, Taipei 10764, Taiwan
关键词
D O I
10.1039/b715253a
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
CdSe quantum dots have been encapped with aromatic ligands: alpha-toluenethiol, thiophenol, and p-hydroxythiophenol to enhance the photoluminescence (PL) quenching and photoelectric properties of the quantum dots. The aromatic ligand capped CdSe quantum dots are prepared through ligand exchange with trioctylphosphine oxide (TOPO) capped CdSe quantum dots. The XPS surface chemistry analysis and elemental analysis has confirmed the success of ligand exchange from TOPO to aromatic ligands. Both XRD and HRTEM-SAED studies indicate the crystalline structure of CdSe quantum dots not only remains but is also improved by the ligand exchange of TOPO with thiol molecules. Time resolved PL decay measurements indicate thiophenol and p-hydroxythiophenol ligands effectively quench the emission and have much shorter PL lifetimes than that of TOPO and that of alpha-toluenethiol. Thus, both thiophenol and p-hydroxythiophenol can act as an effective acceptor for photogenerated holes through aromatic p-electrons. Thiophenol also exhibits good charge transport behavior showing a 10-fold increase in short circuit current density (I-sc) as compared with TOPO in the photocurrent study of fabricated photovoltaic devices.
引用
收藏
页码:675 / 682
页数:8
相关论文
共 70 条
[1]   Self-assembly of a two-dimensional superlattice of molecularly linked metal clusters [J].
Andres, RP ;
Bielefeld, JD ;
Henderson, JI ;
Janes, DB ;
Kolagunta, VR ;
Kubiak, CP ;
Mahoney, WJ ;
Osifchin, RG .
SCIENCE, 1996, 273 (5282) :1690-1693
[2]  
Angelis B. A. D., 1991, APPL SURF SCI, V51, P177
[3]   Forster energy transfer from blue-emitting polymers to colloidal CdSe/ZnS core shell quantum dots [J].
Anni, M ;
Manna, L ;
Cingolani, R ;
Valerini, D ;
Cretí, A ;
Lomascolo, M .
APPLIED PHYSICS LETTERS, 2004, 85 (18) :4169-4171
[4]   Effects of surface functional groups on protein adsorption and subsequent cell adhesion using self-assembled monolayers [J].
Arima, Yusuke ;
Iwata, Hiroo .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (38) :4079-4087
[5]   Highly fluorescent streptavidin-coated CdSe nanoparticles:: Preparation in water, characterization, and micropatterning [J].
Bäumle, M ;
Stamou, D ;
Segura, JM ;
Hovius, R ;
Vogel, H .
LANGMUIR, 2004, 20 (10) :3828-3831
[6]   LUMINESCENCE PROPERTIES OF CDSE QUANTUM CRYSTALLITES - RESONANCE BETWEEN INTERIOR AND SURFACE LOCALIZED STATES [J].
BAWENDI, MG ;
CARROLL, PJ ;
WILSON, WL ;
BRUS, LE .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (02) :946-954
[7]   Surface-modified nanoparticles via thermal and Cu(I)-mediated "click" chemistry:: Generation of luminescent CdSe nanoparticles with polar ligands guiding supramolecular recognition [J].
Binder, Wolfgang H. ;
Sachsenhofer, Robert ;
Straif, Christoph J. ;
Zirbs, Ronald .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (20) :2125-2132
[8]  
BOWENKATARI JE, 1994, J PHYS CHEM-US, V98, P4109
[9]  
Briggs D., 1993, PRACTICAL SURFACE AN, V1
[10]   Semiconductor nanocrystals as fluorescent biological labels [J].
Bruchez, M ;
Moronne, M ;
Gin, P ;
Weiss, S ;
Alivisatos, AP .
SCIENCE, 1998, 281 (5385) :2013-2016