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Xiaogang Peng

Publications and source records attributed to Xiaogang Peng.

At least 19 recordsLinked to original sources
PubMed2006

Formation of nearly monodisperse In2O3 nanodots and oriented-attached nanoflowers: hydrolysis and alcoholysis vs pyrolysis.

Single crystalline and nearly monodisperse In2O3 nanocrystals with both dot and flower shapes were synthesized in a simple reaction system. This system used indium carboxylates as the precursors with or without alcohol as the activating reagents in a hydrocarbon solvent under elevated temperatures. Limited ligand protection (LLP) led to three-dimensional (3D) oriented attachment of nanodots, resulting in 3D nanoflowers. When the system had sufficient ligand protection for the nanocrystals, nanodots were found to be the stable products. The diameters of nearly monodisperse nanodots and nanoflowers were varied in a range from approximately 5 to approximately 15 nm and approximately 15 to approximately 60 nm, respectively. The simple reaction system made it possible to have a systematic study of the reaction mechanisms along with the growth kinetics of nanocrystals. Hydrolysis and alcoholysis were identified as the major paths for this system, as opposed to pyrolysis. Both nearly monodispersed nanodots and nanoflowers can be made through either of the reaction pathways. Hydrolysis was found as a reversible pathway, and alcoholysis was confirmed to be irreversible. Consequently, a sufficient amount of alcohol was able to force the yield of nanocrystals, both dots and flowers, to unity.

Journal Article↗
PubMed2006

Highly luminescent, stable, and water-soluble CdSe/CdS core-shell dendron nanocrystals with carboxylate anchoring groups.

A dendron ligand with two carboxylate anchoring groups at its focal point and eight hydroxyl groups as its terminal groups was found to efficiently convert as-synthesized CdSe/CdS core-shell nanocrystals in toluene to water-soluble dendron-ligand stabilized nanocrystals (dendron nanocrystals). The resulting dendron nanocrystals retained 60% of the photoluminescence value of the original CdSe/CdS core-shell nanocrystals in toluene and were significantly brighter than the similar dendron nanocrystals with thiolate (deprotonated thiol group) as the anchoring group which retained just 10% of the photoluminescence value of the original CdSe/CdS core-shell nanocrystals in toluene. The carboxylate-based dendron nanocrystals survived UV irradiation in air for at least 13 days, about 9 times better than the thiolate-based dendron nanocrystals (35 h) and similar to that of the thiolate-based dendron-box stabilized CdSe/CdS core-shell nanocrystals (box nanocrystals). Upon UV irradiation, the dendron nanocrystals became even 2 times brighter than the original CdSe/CdS core-shell nanocrystals in toluene, and the UV-brightened PL can retain the brightness for at least several months. These stable and bright dendron nanocrystals were soluble in various aqueous media, including all common biological buffer solutions tested, for at least 1.5 years. In addition to their superior performance, the synthetic chemistry of carboxylate dendron ligands and the corresponding dendron nanocrystals is relatively simple and with high yield.

Cadmium Compounds↗
PubMed2006

Colloidal CdSe quantum wires by oriented attachment.

We report here a relatively low temperature (100-180 degrees C) synthetic route to high-quality and single-crystalline CdSe nanowires using air-stable and generic chemicals. The diameter of nanowires was controlled and varied in an exceptionally small size regime, between 1.5 and 6 nm. This was achieved by using alkylamines, a single type or a mixture of two different types of amines, with different chain lengths and varying the reaction temperature. The experimental results suggest the coexistence of two types of fragments in the prewire aggregates, known as "pearl-necklace" or "string-of-pearls" in the literature, which are loosely associated and chemically fused sections.

Anisotropy↗
PubMed2005

An alternative of CdSe nanocrystal emitters: pure and tunable impurity emissions in ZnSe nanocrystals.

The concept, decoupling doping from nucleation and/or growth, allows us to dope nearly all nanocrystals in a given sample which is indicated by complete quenching of the host emission and bright emission from the dopants at characteristic wavelengths tunable in most parts of the visible window using a ZnSe host. In an extreme case, ZnSe coated MnSe nanocrystals (MnSe:ZnSe) emit similarly as commonly known doped nanocrystals. In comparison with CdSe nanocrystals, these alternative emitters not only are intrinsically less toxic but also show some unexpected and expected advantages: stable against thermal and environmental changes, zero reabsorption, and no Forster energy transfer. In addition to their applications to replace CdSe based nanocrystal emitters, the unique structure and properties of the doped nanocrystals are of interest for studying fundamental issues in the field.

Journal Article↗
PubMed2005

Side reactions in controlling the quality, yield, and stability of high quality colloidal nanocrystals.

Effects of side reactions during the formation of high quality colloidal nanocrystals were studied using ZnO as a model system. In this case, an irreversible side reaction, formation of esters, was identified to accompany formation of ZnO nanocrystals through the chemical reaction between zinc stearate and an excess amount of alcohols in hydrocarbon solvents at elevated temperatures. This irreversible side reaction made the resulting nanocrystals stable and with nearly unity yield regardless of their size, shape, and size/shape distribution. Ostwald ripening and intraparticle ripening were stopped due to the extremely low solubility/stability of the possible monomers because all free ligands in the solution were consumed by the side reaction. However, focusing on size distribution and 1D growth that are needed for the growth of high quality nanocrystals could still occur for high yield reactions. Upon the addition of a small amount of stearic acid or phosphonic acid, immediate partial dissolution of ZnO nanocrystals took place. Although the excess alcohol could not react with the resulting zinc phosphonic acid salt, it could force the newly formed zinc stearate gradually but completely back onto the existing nanocrystals. The results in this report indicate that side reactions are extremely important for the formation of high quality nanocrystals by affecting their quality, yield, and stability under growth conditions. Due to their lack of information in the literature and obvious practical advantages, studies of side reactions accompanying formation of nanocrystals are important for both fundamental science related to crystallization and industrial production of high quality nanocrystals.

Colloids↗
PubMed2005

Coupled and decoupled dual quantum systems in one semiconductor nanocrystal.

Dual quantum systems, 0-dimensional quantum dot, and 2-dimensional quantum wells were constructed in one II-VI semiconductor nanocrystal by the epitaxial growth of a barrier (ZnS) layer between the systems in solution. By alteration of the thickness of the barrier layer, the two quantum systems were controlled to either electronically coupled or decoupled. Evidence of optical coupling between the two band gap emissions was also observed. The position and relative intensity of the two emissions can be independently tuned by reaction conditions. Total photoluminescence quantum efficiency of the dual emitting bands reached as high as 30% at room temperature under synthetic conditions not optimized for high emission.

Journal Article↗
PubMed2005

Size-dependent dissociation pH of thiolate ligands from cadmium chalcogenide nanocrystals.

A method, pseudo steady-state titration, is introduced for determining the precipitation pH of nanocrystals coated by electron-donating ligands. CdSe nanocrystals coated with hydrophilic deprotonated thiol (thiolate) ligands were studied systematically. For comparison, CdTe and CdS nanocrystals coated with the same types of ligands were also examined. The results show that the precipitation of the nanocrystals is caused by the dissociation of the nanocrystal-ligand coordinating bonds from the nanocrystal surface. The ligands are removed from the surface due to protonation in a relatively low pH range, between 2 and 7 depending on the size, approximately within the quantum confinement size regime, and chemical composition (band gap) of the nanocrystals. In contrast, the redispersion of the nanocrystals was found to be solely determined by the deprotonation of the ligands. The size-dependent dissociation pH of the ligands was tentatively used as a means for determining the size-dependent free energy associated with the formation of a nanocrystal-ligand coordinating bond.

Cadmium↗
PubMed2005

Bioreactive surfaces prepared via the self-assembly of dendron thiols and subsequent dendrimer bridging reactions.

Here, we report a novel route to prepare bioreactive surfaces on gold by the self-assembly of generation-three hydroxyl-terminated dendron thiols (G3-OH) and subsequent bridging reactions using generation-two amine-terminated dendrimers (G2-NH(2)). It has been shown that G3-OH dendron thiols form a stable and uniform self-assembled monolayer on gold, which can be activated by the homobifunctional cross-linker N,N-disuccinimidyl carbonate (DSC). Subsequent derivatization of the activated monolayer via dendrimer bridging reactions with G2-NH(2) enhances the stability, reactivity, and versatility of the prepared surface. Each step of the surface formation reaction has been monitored, and the resulting surface has been characterized by wetting, electrochemistry, scanning tunneling microscopy (STM), and infrared (IR) spectroscopy measurements. The reactivity of this surface was demonstrated by a Schiff base coupling reaction with 4-cyanobenzaldehyde, by immobilizing biotin molecules onto the peripheral amine groups using one of the conjugation methods, and by further binding avidin onto the biotinylated surface. We believe that the prepared bioreactive surface with a high density of amine groups will be useful for the immobilization of biological macromolecules for various biosensor applications, such as the fabrication of DNA microarrays and protein chips.

Amides↗
PubMed2004

Photocatalytic activity of gold nanocrystals and its role in determining the stability of surface thiol monolayers.

Colloidal gold nanocrystals were found to be efficient photocatalysts for the oxidation of thiols to the corresponding disulfide in aqueous solution under UV radiation, although no noticeable catalytic effect of gold nanocrystals was observed under dark conditions for the same process. The turnover number per particle increased with the size of the nanocrystals and reached 1200 molecules/s for 45-nm gold nanocrystals. The photochemical instability of colloidal gold nanocrystals coated by thiol ligands was found to be determined by the photocatalytic oxidation of the thiol ligands.

Catalysis↗
PubMed2003

Single-phase and gram-scale routes toward nearly monodisperse Au and other noble metal nanocrystals.

Single-phase approaches are introduced for the synthesis of nearly monodisperse Au and other noble metal nanocrystals. The new approaches possess all the advantages of the popular Brust method. With weak ligands or surfactants for the metal ions, the control of the size and size distribution of the nanocrystals in synthesis in the size range between 1 and 15 nm was achieved via maintaining balanced nucleation and growth by tuning the activities of the metal precursors and reducing reagents. Because only weak ligands are employed in the new synthetic schemes, surface modification and functionalization of the resulting nanocrystals can be readily carried out.

Journal Article↗
PubMed2003

Large-scale synthesis of nearly monodisperse CdSe/CdS core/shell nanocrystals using air-stable reagents via successive ion layer adsorption and reaction.

Successive ion layer adsorption and reaction (SILAR) originally developed for the deposition of thin films on solid substrates from solution baths is introduced as a technique for the growth of high-quality core/shell nanocrystals of compound semiconductors. The growth of the shell was designed to grow one monolayer at a time by alternating injections of air-stable and inexpensive cationic and anionic precursors into the reaction mixture with core nanocrystals. The principles of SILAR were demonstrated by the CdSe/CdS core/shell model system using its shell-thickness-dependent optical spectra as the probes with CdO and elemental S as the precursors. For this reaction system, a relatively high temperature, about 220-240 degrees C, was found to be essential for SILAR to fully occur. The synthesis can be readily performed on a multigram scale. The size distribution of the core/shell nanocrystals was maintained even after five monolayers of CdS shell (equivalent to about 10 times volume increase for a 3.5 nm CdSe nanocrystal) were grown onto the core nanocrystals. The epitaxial growth of the core/shell structures was verified by optical spectroscopy, TEM, XRD, and XPS. The photoluminescence quantum yield (PL QY) of the as-prepared CdSe/CdS core/shell nanocrystals ranged from 20% to 40%, and the PL full-width at half-maximum (fwhm) was maintained between 23 and 26 nm, even for those nanocrystals for which the UV-vis and PL peaks red-shifted by about 50 nm from that of the core nanocrystals. Several types of brightening phenomena were observed, some of which can further boost the PL QY of the core/shell nanocrystals. The CdSe/CdS core/shell nanocrystals were found to be superior in comparison to the highly luminescent CdSe plain core nanocrystals. The SILAR technique reported here can also be used for the growth of complex colloidal semiconductor nanostructures, such as quantum shells and colloidal quantum wells.

Journal Article↗
PubMed2003

Luminescent CdSe/CdS core/shell nanocrystals in dendron boxes: superior chemical, photochemical and thermal stability.

The surface ligands, generation-3 (G3) dendrons, on each semiconductor nanocrystal were globally cross-linked through ring-closing metathesis (RCM). The global cross-linking of the dendron ligands sealed each nanocrystal in a dendron box, which yielded box-nanocrystals. Although the dendron ligands coated CdSe nanocrystals (CdSe dendron-nanocrystals) were already quite stable, the stability of CdSe box-nanocrystals against chemical, photochemical, and thermal treatments were dramatically improved in comparison to that of the original dendron-nanocrystals. Furthermore, the box structure of the ligands monolayer coupled with the stable inorganic CdSe/CdS core/shell nanocrystals resulted in a class of extremely stable nanocrystal/ligands complexes. The band edge photoluminescence of the core/shell dendron-nanocrystals and box-nanocrystals were partially remained, and could be further brightened through controlled chemical oxidation or photooxidation. Practically, the stability of the box-nanocrystals is sufficient for most fundamental studies and technical applications. The box-nanocrystals may represent a general solution for the commonly encountered instability for many types of colloidal nanocrystals. The size distribution of the empty dendron boxes formed by the dissolution of the inorganic nanocrystals in concentrated HCl was very narrow. The empty boxes as new types of polymer capsules are soluble in solution, mesoporous, and with a very thin but stable peripheral. Those nanometer-sized cavities should be of interest for many purposes in the field of solution host-guest chemistry.

Journal Article↗
PubMed2002

Nearly monodisperse and shape-controlled CdSe nanocrystals via alternative routes: nucleation and growth.

The nucleation and growth of colloidal CdSe nanocrystals with a variety of elongated shapes were explored in detail. The critical size nuclei for the system were magic sized nanoclusters, which possessed a sharp and dominated absorption peak at 349 nm. The formation of the unique magic sized nuclei in a broad monomer concentration range was not expected by the classic nucleation theory. We propose that this was a result of the extremely high chemical potential environment, that is, very high monomer concentrations in the solution, required for the growth of those elongated nanocrystals. The shape, size, and size/shape distributions of the resulting nanocrystals were all determined by two related factors, the magic sized nuclei and the concentration of the remaining monomers after the initial nucleation stage. Without any size sorting, nearly monodisperse CdSe quantum structures with different shapes were reproducibly synthesized by using the alternative cadmium precursors, cadmium-phosphonic acid complexes. A reasonably large excess of the cadmium precursor, which is less reactive than the Se precursor, was found beneficial for the system to reach the desired balance between nucleation and growth. The shape evolution and growth kinetics of these elongated nanocrystals were consistent with the diffusion-controlled model proposed previously. The branched nanocrystals had to grow at very high monomer concentrations because the multiple growth centers at the end of each branch must be fed with a very high diffusion flux to keep all branches in the 1D-growth mode. The rice-shaped nanocrystals were found as special products of the 3D-growth stage. The growth of the nanocrystals in the 1D-growth stage was proven to be not unidirectional after the length of the nanocrystals reached a certain threshold. Experimental results indicate that coordinating solvents and two ligands with distinguishable coordinating abilities are both not intrinsic requirements for the growth of elongated CdSe nanocrystals.

Journal Article↗
PubMed2002

Stabilization of inorganic nanocrystals by organic dendrons.

A series of hydrophilic organic dendron ligands was designed and synthesized for stabilizing high-quality semiconductor and noble metal nanocrystals. The focal point of the dendron ligands is chosen to be a thiol group which is a universal coordinating site for compound semiconductor and noble metal nanocrystals. The methods for binding these dendron ligands onto the surface of the nanocrystals are simple and straightforward. The thin, about 1-2 nm, but closely packed and tangled ligand shell provides sufficient stability for the "dendron-protected nanocrystals" to withstand the rigors of the coupling chemistry and the standard separation/purification techniques. The chemistry presented can be immediately applied for the development of a new generation of biomedical labeling reagents based on high-quality semiconductor nanocrystals. It also provides an alternative path to apply noble metal nanocrystals for developing sensitive detection schemes for chemical and biochemical purposes. The concept may further provide an optimal solution for many other problems encountered in nanocrystal-related research and development, for which the stability of the nanocrystals is a critical issue. Furthermore, the experimental results confirmed that the photochemical stability of colloidal semiconductor and noble metal nanocrystals is the key for developing reliable and reproducible processing chemistry for these nanocrystals.

Journal Article↗