Publications

2006
Tsiala Saraidarov, Renata Reisfeld, Miri Kazes, and Uri Banin. 2006. “Blue laser dye spectroscopic properties in solgel inorganic-organic hybrid films.” Optics letters, 31, 3, Pp. 356-358. Publisher's Version Abstract

A blue solid-state laser material based on 4,4′4′ dibenzyl carbamido stilbene-2,2′2′ disulfonic acid incorporated into solgel zirconia and inorganic–organic hybrid matrices is presented. The absorption maxima of the dye in various matrices are around 339–361 nm, and the broad fluorescence peaks are at 411–413 nm. Optical gain measurements using the variable stripe method show amplified spontaneous emission peaking at 437 nm.

Asaf Salant, Ella Amitay-Sadovsky, and Uri Banin. 2006. “Directed self-assembly of gold-tipped CdSe nanorods.” Journal of the American Chemical Society, 128, 31, Pp. 10006-10007. Publisher's Version Abstract

Abstract Image

Gold-tipped CdSe rods (nanodumbbells) were solubilized in an aqueous phase and self-assembled in a head-to-tail manner using biotin disulfide and avidin. The disulfide end of the biotin molecule attaches to the gold tip of the nanodumbbell, and the biotin end of the molecule is able to conjugate to an avidin protein. The avidin can strongly conjugate up to four biotin molecules. Changing the ratios of biotin to nanodumbbells leads to the formation of dimers, trimers, and flowerlike structures. To further improve the distribution of chain lengths, a separation method based upon weight was applied using a concentration gradient. The gold tips provide effective anchor points for constructing complex nanorod structures by self-assembly.

Dov Steiner, Assaf Aharoni, Uri Banin, and Oded Millo. 2006. “Level structure of InAs quantum dots in two-dimensional assemblies.” Nano letters, 6, 10, Pp. 2201-2205. Publisher's Version Abstract

The electronic level structure of colloidal InAs quantum dots (QDs) in two-dimensional arrays, forming a QD-solid system, was probed using scanning tunneling spectroscopy. The band gap is found to reduce compared to that of the corresponding isolated QDs. Typically, the electron (conduction-band) ground state red shifts more than the hole (valence-band) ground state. This is assigned to the much smaller effective mass of the electrons, resulting in stronger electron delocalization and larger coupling between electron states of neighboring QDs compared to the holes. This is corroborated by comparing these results with those for InAs and CdSe nanorod assemblies, manifesting the effects of the electron effective mass and arrangement of nearest neighbors on the band gap reduction. In addition, in InAs QD arrays, the levels are broadened, and in some cases their discrete level structure was nearly washed out completely and the tunneling spectra exhibited a signature of two-dimensional density of states.

Dan Oron, Miri Kazes, Itzik Shweky, and Uri Banin. 2006. “Multiexciton spectroscopy of semiconductor nanocrystals under quasi-continuous-wave optical pumping.” Physical Review B, 74, 11, Pp. 115333. Publisher's Version Abstract

We present a method for performing multiexciton spectroscopy in colloidal semiconductor nanocrystals. In this regime multiexcitonic states are generated sequentially via a “ladder-climbing” mechanism. The distribution of multiexcitonic states, determined by a steady-state rate equation, adiabatically follows the illumination intensity, allowing for “slow” detection of multiexcitonic spectra. Emission spectra of multiexcitonic states with a small number of excitons are obtained without passing through states with a large number of excitons. This is in contrast with impulsive excitation schemes utilizing picosecond pulses, where in order to significantly populate a given multiexcitonic state, many of the dots necessarily pass through states with a larger number of excitons due to the Poissonian distribution of the number of absorbed photons. In particular, we observe directly the order of appearance of the various multiexcitonic peaks. This enables us to determine the threshold conditions for Auger ionization, shedding more light on the nature of this process. We are also able to observe the short-lived excitations at higher energies than triexcitons in CdSe quantum dots. Finally, we demonstrate bi- and triexcitonic optical gain in a close-packed film under quasi-continuous-wave pumping.

Ron Gill, Ronit Freeman, Jian-Ping Xu, Itamar Willner, Shira Winograd, Itzik Shweky, and Uri Banin. 2006. “Probing Biocatalytic Transformations with CdSe− ZnS QDs.” Journal of the American Chemical Society, 128, 48, Pp. 15376-15377. Publisher's Version Abstract

CdSe/ZnS QDs enable the optical probing of the biocatalytic oxidation of tyrosine derivatives and of the scission of peptides by thrombin. CdSe/ZnS QDs were modified with tyrosine methyl ester or with a tyrosine-containing peptide. The tyrosine units were reacted with tyrosinase/O2 to yield the respective l-DOPA and quinone derivatives. The luminescence of QDs modified by the enzyme-generated quinone units is quenched. The quinone-functionalized peptide associated with the QDs was cleaved by thrombin, a process that restored the luminescence of the QDs.

Dong Hee Son, Joshua S Wittenberg, Uri Banin, and Paul A Alivisatos. 2006. “Second harmonic generation and confined acoustic phonons in highly excited semiconductor nanocrystals.” The Journal of Physical Chemistry B, 110, 40, Pp. 19884-19890. Publisher's Version Abstract

The photo-induced enhancement of second harmonic generation and the effect of nanocrystal shape and pump intensity on confined acoustic phonons in semiconductor nanocrystals have been investigated with time-resolved scattering and absorption measurements. The second harmonic signal showed a sublinear increase of the second-order susceptibility with respect to the pump pulse energy, indicating a reduction of the effective one-electron second-order nonlinearity with increasing electron−hole density in the nanocrystals. The coherent acoustic phonons in spherical and rod-shaped semiconductor nanocrystals were detected in a time-resolved absorption measurement. Both nanocrystal morphologies exhibited oscillatory modulation of the absorption cross section, the frequency of which corresponded to their coherent radial breathing modes. The amplitude of the oscillation also increased with the level of photoexcitation, suggesting an increase in the amplitude of the lattice displacement as well.

Yuval Ebenstein, Eyal Yoskovitz, Ronny Costi, Assaf Aharoni, and Uri Banin. 2006. “Interaction of scanning probes with semiconductor nanocrystals; physical mechanism and basis for near-field optical imaging.” The Journal of Physical Chemistry A, 110, 27, Pp. 8297-8303. Publisher's Version Abstract

We investigate the modification of photoluminescence (PL) from single semiconductor nanocrystal quantum dots (NCs) in the proximity of metal and semiconducting atomic force microscope (AFM) tips. The presence of the tip alters the radiative decay rate of an emitter via interference and opens efficient nonradiative decay channels via energy transfer to the tip material. These effects cause quenching (or enhancement) of the emitter's PL intensity as a function of its distance from the interacting tip. We take advantage of this highly distance-dependent effect to realize a contrast mechanism for high-resolution optical imaging. AFM tips are optimized as energy acceptors by chemical functionalization with InAs NCs to achieve optical resolution down to 30 nm. The presented experimental scheme offers high-resolution optical information while maintaining the benefits of traditional AFM imaging. We directly measure the PL intensity of single NCs as a function of the tip distance. Our results are in good agreement with calculations made by a classical theoretical model describing an oscillating dipole interacting with a planar mirror.

Itzhak Shweky, Assaf Aharoni, Taleb Mokari, Eli Rothenberg, Moshe Nadler, Inna Popov, and Uri Banin. 2006. “Seeded growth of InP and InAs quantum rods using indium acetate and myristic acid.” Materials Science and Engineering: C, 26, 5-7, Pp. 788-794. Publisher's Version Abstract

A synthesis of soluble III–V semiconductor quantum rods using gold nanoparticles to direct and catalyze one-dimensional growth isdeveloped. The growth takes place via the solution–liquid–solid (SLS) mechanism where proper precursors are injected into a coordinatingsolvent. We report the synthesis of InP nanorods using indium acetate and myristic acid with gold nanoparticles as the catalysts in the SLS growthmode. A similar route was successfully developed for the growth of InAs nanorods. We find that the amount of Au catalyst in the reaction is animportant parameter to achieve shape control. Transmission electron microscope (TEM) images of InP and InAs nanocrystals revealed that thecrystals are mostly rod-shaped, and provide strong evidence for Au presence in one edge. The rods were characterized structurally using X-raydiffraction and high-resolution TEM and optically by absorption and photoluminescence.D2005 Elsevier B.V. All rights reserved.

Aaron E Saunders, Inna Popov, and Uri Banin. 2006. “Synthesis of hybrid CdS− Au colloidal nanostructures.” The Journal of Physical Chemistry B, 110, 50, Pp. 25421-25429. Publisher's Version Abstract

We explore the growth mechanism of gold nanocrystals onto preformed cadmium sulfide nanorods to form hybrid metal nanocrystal/semiconductor nanorod colloids. By manipulating the growth conditions, it is possible to obtain nanostructures exhibiting Au nanocrystal growth at only one nanorod tip, at both tips, or at multiple locations along the nanorod surface. Under anaerobic conditions, Au growth occurs only at one tip of the nanorods, producing asymmetric structures. In contrast, the presence of oxygen and trace amounts of water during the reaction promotes etching of the nanorod surface, providing additional sites for metal deposition. Three growth stages are observed when Au growth is performed under air:  (1) Au nanocrystal formation at both nanorod tips, (2) growth onto defect sites on the nanorod surface, and finally (3) a ripening process in which one nanocrystal tip grows at the expense of the other particles present on the nanorod. Analysis of the hybrid nanostructures by high-resolution TEM shows that there is no preferred orientation between the Au nanocrystal and the CdS nanorod, indicating that growth is nonepitaxial. The optical signatures of the nanocrystals and the nanorods (i.e., the surface plasmon and first exciton transition peaks, respectively) are spectrally distinct, allowing the different stages of the growth process to be easily monitored. The initial CdS nanorods exhibit band gap and trap state emission, both of which are quenched during Au growth.