End-to-End Assembly of Shape-Controlled Nanocrystals via a Nanowelding Approach Mediated by Gold Domains.

[*] Dr. A. Figuerola, I. R. Franchini, A. Fiore, Dr. S. Kudera, Prof. R. Cingolani, Dr. L. Manna National Nanotechnology Laboratory of CNR-INFM, Unita di Ricerca IIT Distretto Tecnologico ISUFI, via per Arnesano km 5, I-73100 Lecce (Italy) Fax: (þ39) 0832298237 E-mail: [email protected] Dr. A. Figuerola, A. Fiore, R. Mastria, Prof. R. Cingolani Scuola Superiore ISUFI; University of Salento Distretto Tecnologico ISUFI, via per Arnesano km 5, I-73100 Lecce (Italy

Temperature and Size Dependence of the Optical Properties of Tetrapod-Shaped Colloidal Nanocrystals Exhibiting Type-II Transitions

We have investigated the optical properties of colloidal seed-grown CdSe (seed)/CdTe (arms) nanotetrapods both experimentally and computationally. The tetrapods exhibit a type-II transition arising from electrons localized in the CdSe seed region and holes delocalized in the CdTe arms, along with a residual type-I recombination in long-arm tetrapods. Experiments and theory helped to identify the origin of both types of transitions and their size dependence. In particular, time-resolved experiments performed at 10 K evidenced a size-dependent, long living type-II radiative emission arising from the peculiar electron–hole wave function localization. Temperature-dependent photoluminescence (PL) studies indicate that, at high temperature (>150 K), the main process limiting the PL quantum efficiency of the type-I PL is thermal escape of the charge carriers through efficient exciton-optical phonon coupling. The type-II PL instead is limited both by thermal escape and by the promotion of electrons from the condu..

"Nanohybrids" based on pH-responsive hydrogels and inorganic nanoparticles for drug delivery and sensor applications.

Allyl-PEG capped inorganic NPs, including magnetic iron oxide (IONPs), fluorescent CdSe/ZnS quantum dots (QDs), and metallic gold (AuNPs of 5 and 10 nm) both individually and in combination, were covalently attached to pH-responsive poly(2-vinylpyridine-co-divinylbenzene) nanogels via a facile and robust one-step surfactant-free emulsion polymerization procedure. Control of the NPs associated to the nanogels was achieved by the late injection of the NPs to the polymerization solution at a stage when just polymeric radicals were present. Remarkably, by varying the total amount of NPs injected, the swelling behavior could be affected. Furthermore, the magnetic response as well as the optical features of the nanogels containing either IONPs or QDs could be modified. In addition, a radical quenching in case of gold nanoparticles was observed, thus affecting the final nanogel geometry

Colloidal PbTe-Au nanocrystal heterostructures

Colloidal PbTe nanocrystals are reacted with AuCl(3) in the presence of dodecylamine and tetraoctylammonium bromide in a toluene solution. At room temperature, only homogenous nucleation of isolated Au nanocrystals in solution is observed. At higher temperatures (i.e. 60 degrees C or higher) the gold ions/atoms are able to diffuse through the PbTe nanocrystals and to form one or more metallic gold regions inside them, while most of the remaining volume of each nanocrystal becomes amorphous. Longer reaction times lead to the growth of a single balloon-shaped Au domain attached via its apex to the surface of each nanocrystal. The structural and compositional quantification of the starting PbTe nanocrystals and of the various reaction products is often complicated by several reactive processes occurring during in situ analysis by electron microscopy. Evidences of the formation of a metastable Au(3)Te compound are presented

"Nanohybrids" Based on pH-Responsive Hydrogels and Inorganic Nanoparticles for Drug Delivery and Sensor Applications

Allyl-PEG capped inorganic NPs, including magnetic iron oxide (IONPs), fluorescent CdSe/ZnS quantum dots (QDs), and metallic gold (AuNPs of 5 and 10 nm) both individually and in combination, were covalently attached to pH-responsive poly(2-vinylpyridine-co-divinylbenzene) nanogels via a facile and robust one-step surfactant-free emulsion polymerization procedure. Control of the NPs associated to the nanogels was achieved by the late injection of the NPs to the polymerization solution at a stage when just polymeric radicals were present. Remarkably, by varying the total amount of NPs injected, the swelling behavior could be affected. Furthermore, the magnetic response as well as the optical features of the nanogels containing either IONPs or QDs could be modified. In addition, a radical quenching in case of gold nanoparticles was observed, thus affecting the final nanogel geometry

Phototransport in networks of tetrapod-shaped colloidal semiconductor nanocrystals

Tetrapod-shaped CdSe(core)/CdTe(arms) colloidal nanocrystals, capped with alkylphosphonic acids or pyridine, were reacted with various small molecules (acetic acid, hydrazine and chlorosilane) which induced their tip-to-tip assembly into soluble networks. These networks were subsequently processed into films by drop casting and their photoconductive properties were studied. We observed that films prepared from tetrapods coated with phosphonic acids were not photoconductive, but tip-to-tip networks of the same tetrapods exhibited appreciable photocurrents. On the other hand, films prepared from tetrapods coated with pyridine instead of phosphonic acids were already highly photoconductive even if the nanocrystals were not joined tip-to-tip. Based on the current-voltage behavior under light we infer that the tunneling between tetrapods is the dominant charge transport mechanism. In all the samples, chemically-induced assembly into networks tended to reduce the average tunneling barrier. Additionally, pyridine-coated tetrapods and the tip-to-tip networks made out of them were tested as active materials in hybrid photovoltaic devices. Overall, we introduce an approach to chemically-induced tip-to-tip assembly of tetrapods into solution processable networks and demonstrate the enhancement of electronic coupling of tetrapods by various ligand exchange procedures

End-to-End Assembly of Shape-Controlled Nanocrystals via a Nanowelding Approach Mediated by Gold Domains

Welding nanocrystals for assembly: The welding of Au domains grown on the tips of shape-controlled cadmium chalcogenide colloidal nanocrystals is used as a strategy for their assembly. Iodine-induced coagulation of selectively grown Au domains leads to assemblies such as flowerlike structures based on bullet-shaped nanocrystals, linear and cross-linked chains of nanorods, and globular networks with tetrapods as building blocks

Phototransport in networks of tetrapod-shaped colloidal semiconductor nanocrystals

Tetrapod-shaped CdSe(core)/CdTe(arms) colloidal nanocrystals, capped with alkylphosphonic acids or pyridine, were reacted with various small molecules (acetic acid, hydrazine and chlorosilane) which induced their tip-to-tip assembly into soluble networks. These networks were subsequently processed into films by drop casting and their photoconductive properties were studied. We observed that films prepared from tetrapods coated with phosphonic acids were not photoconductive, but tip-to-tip networks of the same tetrapods exhibited appreciable photocurrents. On the other hand, films prepared from tetrapods coated with pyridine instead of phosphonic acids were already highly photoconductive even if the nanocrystals were not joined tip-to-tip. Based on the current-voltage behavior under light we infer that the tunneling between tetrapods is the dominant charge transport mechanism. In all the samples, chemically-induced assembly into networks tended to reduce the average tunneling barrier. Additionally, pyridine-coated tetrapods and the tip-to-tip networks made out of them were tested as active materials in hybrid photovoltaic devices. Overall, we introduce an approach to chemically-induced tip-to-tip assembly of tetrapods into solution processable networks and demonstrate the enhancement of electronic coupling of tetrapods by various ligand exchange procedures