FRET and ligand related NON-FRET processes in single quantum dot-perylene bisimide assemblies

被引:57
作者
Kowerko, Danny [1 ]
Schuster, Joerg [1 ]
Amecke, Nicole [1 ]
Abdel-Mottaleb, Mohammed [1 ]
Dobrawa, Rainer [2 ,3 ]
Wuerthner, Frank [2 ,3 ]
von Borczyskowski, Christian [1 ]
机构
[1] Tech Univ Chemnitz, Inst Phys & NanoMA, Ctr Nanostruct Mat & Analyt, D-09107 Chemnitz, Germany
[2] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
[3] Univ Wurzburg, Rontgen Res Ctr Complex Mat Syst, D-97074 Wurzburg, Germany
关键词
RESONANCE ENERGY-TRANSFER; CDSE NANOPARTICLES; ELECTRON-TRANSFER; SOLAR-CELLS; NANOCRYSTALS; PHOTOLUMINESCENCE; SURFACE; NANOASSEMBLIES; INTERMITTENCY; SPECTROSCOPY;
D O I
10.1039/b910308b
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
Nanoassemblies are formed via self-assembly of ZnS capped CdSe quantum dots (QD) and perylene bisimide dyes (PBI). Upon assembly formation with functionalized dye molecules the QD photoluminescence (PL) is quenched. Quenching has been assigned partly to FRET (fluorescence resonance energy transfer) and NON-FRET processes. By means of time resolved single particle spectroscopy of immobilized QD-dye assemblies, it is demonstrated that NON-FRET processes are due to new non-radiative decay channels caused by the assembly formation process itself. Immobilized (single) assemblies exhibit the same processes as ensembles of assemblies in toluene solution. Only one dye molecule on a QD quenches the PL up to 50%, which is much stronger than is expected when replacing a volume related number of ligands. NON-FRET processes are distinct from photoinduced charge and/or energy transfer. A combination of a Stern-Volmer and FRET analysis of ensemble experiments supports the investigation of the dynamics of assembly formation at extremely low concentration ratios of PBI to QD. This allows us to distinguish between the effects of PBI and ligands on PL quenching on a single molecule level which is not possible in conventional ligand dynamic experiments.
引用
收藏
页码:4112 / 4123
页数:12
相关论文
共 43 条
[1]   Identification of surface states on individual CdSe quantum, dots by room-temperature conductance spectroscopy [J].
Alperson, B ;
Rubinstein, I ;
Hodes, G .
PHYSICAL REVIEW B, 2001, 63 (08)
[2]  
[Anonymous], J PHYS CHEM
[3]   Probing Wave Functions at Semiconductor Quantum-Dot Surfaces by Non-FRET Photoluminescence Quenching [J].
Blaudeck, Thomas ;
Zenkevich, Eduard I. ;
Cichos, Frank ;
von Borczyskowski, Christian .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (51) :20251-20257
[4]  
BOULEBAA A, 2007, J AM CHEM SOC, V129, P1532
[5]   The effects of chemisorption on the luminescence of CdSe quantum dots [J].
Bullen, C ;
Mulvaney, P .
LANGMUIR, 2006, 22 (07) :3007-3013
[6]   Power-law intermittency of single emitters [J].
Cichos, F. ;
von Borczyskowski, C. ;
Orrit, M. .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2007, 12 (06) :272-284
[7]  
CICHOS F, 2005, PHYS REV B, V70
[8]   Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors [J].
Clapp, AR ;
Medintz, IL ;
Mauro, JM ;
Fisher, BR ;
Bawendi, MG ;
Mattoussi, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (01) :301-310
[9]   Forster resonance energy transfer investigations using quantum-dot fluorophores [J].
Clapp, AR ;
Medintz, IL ;
Mattoussi, H .
CHEMPHYSCHEM, 2006, 7 (01) :47-57
[10]   Can luminescent quantum dots be efficient energy acceptors with organic dye donors? [J].
Clapp, AR ;
Medintz, IL ;
Fisher, BR ;
Anderson, GP ;
Mattoussi, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (04) :1242-1250