Quantum dots coordinated with conjugated organic ligands: new nanomaterials with novel photophysics
- First Online:
- Cite this article as:
- Hammer, N.I., Emrick, T. & Barnes, M.D. Nanoscale Res Lett (2007) 2: 282. doi:10.1007/s11671-007-9062-8
- 6k Downloads
CdSe quantum dots functionalized with oligo-(phenylene vinylene) (OPV) ligands (CdSe-OPV nanostructures) represent a new class of composite nanomaterials with significantly modified photophysics relative to bulk blends or isolated components. Single-molecule spectroscopy on these species have revealed novel photophysics such as enhanced energy transfer, spectral stability, and strongly modified excited state lifetimes and blinking statistics. Here, we review the role of ligands in quantum dot applications and summarize some of our recent efforts probing energy and charge transfer in hybrid CdSe-OPV composite nanostructures.
KeywordsSingle molecule spectroscopy Hybrid nanomaterial Quantum dot Blinking Conjugated polymer Energy transfer Charge transfer Photovoltaic Atomic force microscope
Over the past several years, semiconductor nanocrystals (quantum dots) have attracted enormous interest in virtually all areas of the physical sciences. The tunable optical and electronic properties of quantum dots make them ideal building blocks in nanoscale photonic, photovoltaic, and light-emitting diode (LED) device applications [1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19]. In addition, their robust photoluminescence makes them attractive for probing dynamics in biological systems at the single molecule level [20, 21, 22, 23]. One of the keys to the successful use of quantum dots in any application is the ability to tailor their surface with ligands. The ligands bound to the surface of quantum dots largely dictate solution properties, and their miscibility in a particular medium including organic solvents, water, and polymer films. The ability to control this surface functionality has been the subject of considerable research in recent years, [21, 24, 25, 26, 27, 28, 29] and promises to direct the feasibility of quantum dots in applications. Here, we summarize some of our recent efforts probing energy and charge transfer between quantum dots and their bound ligands and discuss new possibilities for their use as building blocks in next generation nanoscale devices.
The role of ligands in quantum dot synthesis
The most widely utilized quantum dots to date are II–VI semiconductor nanocrystals such as cadmium selenide, cadmium sulfide, and cadmium telluride. Preparation methods for the synthesis of high quality and nearly monodisperse cadmium selenide quantum dots have typically utilized tri-n-octylphosphine oxide (TOPO) and trioctylphospine (TOP) as these compounds provide the most controlled growth conditions. Prior to the use of TOPO, CdSe nanocrystals were prepared by using organometallic reagents in inverse micellar solution . Bawendi and co-workers showed that injection of the metal-organic precursors into a hot (∼150–300 °C) reaction pot with TOPO and TOP as solvent resulted in a short burst of homogeneous nucleation and a narrow size distribution covered by TOPO ligands . Size-control is primarily achieved by varying the reaction temperature and the initial precursor concentration. Since TOPO serves as the primary surface ligand, the nanoparticles obtained by this method are soluble in hydrophobic solvents such as toluene and hexanes.
Nanocrystal surface defects such as dangling selenide bonds have been described as charge carrier trap sites, and have been associated with less than optimal optical (and device) performance . The objective of increased brightness of photoluminescence (quantum yield) has led to efforts of passivating surface defects with organic or inorganic ligands, either during the synthesis or afterwards. For example, Talapin et al. showed that incorporation of alkylamines, particularly hexadecylamine (HDA), into the synthesis led to much improved quantum yields (as high as 50%) . This dramatic improvement was attributed to the passivation of the cadmium selenide surface defects with the HDA ligands. However, Alivisatos pointed out that it is generally very difficult to simultaneously passivate both anionic and cationic surface sites by organic ligands because there would always remain some dangling bonds . For this reason, inorganic passivation is generally more effective for creating very bright quantum dots. An additional layer (shell) of higher band gap material grown around the surface of the nanocrystal (core) serves to passivate both the anionic and cationic surface dangling bonds in these “core/shell” or “capped” systems. In the case of zinc sulfide (CdSe/ZnS) [33, 35, 36] or cadmium sulfide (CdSe/CdS) [34, 37, 38] coated cadmium selenide quantum dots, much improved photoluminescence properties and photostability is observed with quantum yields of up to 85% in solution . However, this inorganic surface modification creates a new nanocrystal system with properties which are dependent on both core and shell materials. In addition, the shell can serve as an insulating medium that limits electronic communication with surface ligands or the environment.
Ligand functionalization of quantum dots
Ligand exchange typically employs a functional moiety with a high affinity for binding to the surface of quantum dots (B), a spacer group (such as an alkyl or aryl chain, S), and a functional group or chain that possesses the chemical property of interest (F). Thiols have proven useful in ligand exchange due to their high affinity for the particle surface. For example, Chan and Nie used mercaptoacetic acid to render CdSe/ZnS quantum dots soluble in biological (aqueous) media by taking advantage of the fact that the mercapto group would easily bind to a zinc atom . The value of α,ω-thioalkanoic acids is found in part in the chain-end carboxyl group that can be used in coupling to biomolecules. This method has its limitations, however, with inefficient loading of the desired ligands onto the quantum dots and poor long-term stability due to oxidation [24, 25]. Alternatives to thiols include carbodithioates,  dendrons,  peptides, , and oligomeric phosphines . In the case of carbodithioates, nearly quantitatively exchange has been achieved with the initial TOPO surface ligands .
Photophysics of isolated QD-OPV nanostructures
Biological applications of quantum dots
Applications involving quantum dot—ligand combinations are most numerous in the biological arena, especially for imaging and tracking of biological structures or single biomolecules of interest [20, 21, 22]. Conventional organic dyes possess broad emission spectra and narrow absorption profiles. This combination results in fluorescence signal overlap from the different dyes employed and also requires as many excitation sources as the number of dyes used. Quantum dots, on the other hand, possess narrow emission profiles and broad absorption bands. In addition, quantum dots allow for long-term observation of tagged molecules with less photobleaching than seen for conventional organic dyes. Weiss has recently reviewed biologically relevant applications of the many relevant quantum dot—ligand combinations . For example, streptavidin coverage has proven attractive for its use in combination with biotinylated proteins and antibodies .
There has recently been a great deal of interest in energy transfer involving quantum dots and fluorescently-labeled biomolecules [42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55]. Fluorescence resonance energy transfer (FRET) from an excited state donor to an ground state acceptor occurs such that the overlap of the donor’s emission and acceptor’s excitation spectra, and the spatial distance between the two components, determine the efficiency of the energy transfer process . Mattoussi recently reviewed many of the studies of FRET involving quantum dots and biological systems . Bawendi and co-workers first demonstrated FRET energy transfer involving mixtures of different sizes of quantum dots . Emission from smaller, higher energy, quantum dots decreased as emission from the larger, smaller energy level spacing, quantum dots increased. The first observation of FRET between quantum dots and biological molecules was made in 2001 by Van Orden and co-workers . In that study quantum dots with biotinylated bovine serum albumin ligands interacted with streptavidin that was labeled with a rhodamine dye. Emission from the dye was observed to increase as emission from the quantum dot diminished. Kotov and co-workers reported energy transfer to quantum dots from native tryptophan molecules in an interacting protein . Other interesting FRET applications include interactions with metalloproteins  and DNA,  a basis for photodynamic therapy,  and nanosensor design . Ha recently demonstrated FRET between single quantum dots and their ligands,  and Mattoussi reported spectrally resolved energy transfer between quantum dots and fluorescently tagged proteins .
Solid state applications of quantum dots
The optoelectronic properties (broad absorption spectrum and narrow emission profile) of quantum dots make them very attractive building blocks for photovoltaics, [1, 2, 3, 4, 5, 6, 7] lasers, [8, 9, 10, 11] and light emitting diodes (LED) [12, 13, 14, 15, 16, 17, 18, 19]. Energy transfer between quantum dots and other building blocks (such as conjugated organic polymers) that compose such devices has been studied [58, 59, 60, 61, 62]. In addition, unique quantum dot—ligand combinations enable the preparation of novel nanostructure materials. For example, Raymo and co-workers introduced quantum dots with photochromic ligands that allow for a mechanism to activate and suppress energy transfer to the ligands . The same authors also functionalized quantum dots with pH sensitive ligands that allow luminescence switching under chemical stimulation [64, 65].
Enhanced energy transfer in CdSe-OPV nanostructures
In an effort to determine the effects of the bound conjugated organic ligands on individual quantum dot photophysics, single molecule spectroscopic measurements were performed on the CdSe-OPV nanostructures deposited on clean glass coverslips from extremely dilute solutions . A Nikon TE300 inverted microscope with a 1.4NA oil objective was used to obtain single nanostructure fluorescence emission spectra. Spectra were acquired by focusing the CdSe-OPV emission from the side-port of the microscope onto an Acton SP2150i dual-grating spectrograph, and detected with a PI/Acton Pixis 400B back-illuminated CCD camera, with a typical exposure time of 2 s.
Charge transfer in quantum dot applications
Charge transfer between quantum dots and the surrounding environment is the basis for many of the solid state applications involving semiconductor nanocrystals [1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19]. The transfer of electrons (or holes) between a conjugated organic polymer matrix and a quantum dot, for example, enables the flow of charge throughout a device . Lian has written a comprehensive review of this process with respect to these applications . Recently, the transfer of charge carriers between quantum dots and their ligands has led to the development of new analyte sensing protocols [69, 70, 71, 72]. A most exciting area of quantum dot research is related to the use of electron donating organic ligands for blinking suppression [66, 73, 74, 75, 76, 77, 78, 79].
Brus and co-workers first demonstrated that single quantum dots exhibit fluorescence intermittency, or the tendency to blink . Since that time, researchers have studied this phenomenon intensely using various experimental parameters and theoretical models [81, 82, 83, 84, 85, 86, 87]. The most common explanation for blinking in quantum dots revolves around the trapping of exciton charge carriers in surface defects. When a quantum dot is excited, the resulting exciton delocalizes over the volume of the nanocrystal. If the electron or hole becomes “trapped” in a surface defect, photoluminescence ceases.
Recently, Hohng and Ha reported a blinking suppression in solutions of quantum dots . When the individual streptavidin-coated CdSe/ZnS quantum dots were exposed in solution to β-mercaptoethanol, their blinking essentially disappeared and constant radiative emission was observed. The authors determined that only thiol-containing species with short chain lengths were able to suppress the quantum dot blinking. Since thiols are effective electron donors, the authors argued that these ligands donate electrons to fill surface traps. This deactivates the blinking mechanism, and leads to a more constant emission. Tinnefeld and co-workers soon after reported similar blinking suppression using mercaptoethylamine but interpreted their observations as a dramatic increase in the blinking kinetics . In other words, the presence of the ligands perturbed the dynamics of the exciton. Recently, Mulvaney and co-workers were also able to modify the blinking dynamics in quantum dots through the variation in the choice of ligands .
Blinking suppression in CdSe-OPV nanostructures
Summary and outlook
Quantum dots have received much attention in recent years due to their unique photophysical properties. Research into their surface chemistry is driven by the desire to optimize such structures for many applications that seek to take advantage of these photophysical properties. The surface-bound ligands of quantum dots in many ways dictate their success or failure in applications, as the ligands determine the solubility or miscibility in a particular medium, and also mediate energy and charge transfer with the surrounding environment. Interest in both energy and charge transfer between quantum dots and their ligands has grown steadily over the years, and includes the design of novel architectures and hybrid structures that have led to some very exciting phenomena, such as blinking suppression. With the application of a growing list of synthetic methods for the functionalizing of quantum dots, the outlets for such engineered nanostructural components are growing rapidly.
The authors wish to thank the Intelligence Community Postdoctoral Program, the NSF sponsored MRSEC, and the US Department of Energy for financial support of the work described in this account.