Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Alf Mews is active.

Publication


Featured researches published by Alf Mews.


Chemical Physics Letters | 1993

A quantum dot quantum well: CdS/HgS/CdS

Alexander Eychmüller; Alf Mews; Horst Weller

Abstract A wet chemical synthetic route is presented for the preparation of a spherical quantum well. The quantum well consists of a core of size-quantized CdS, a monolayer of HgS and approximately four monolayers of CdS as the outermost shell. The total diameter of these particles exhibiting unique optical properties is about 80 A. The route described opens the way for the generation of quantum dot quantum wells (QDQW) with variable layer thicknesses as well as for compounds composed from more than two materials.


Journal of Applied Physics | 2004

Electroluminescence from isolated CdSe∕ZnS quantum dots in multilayered light-emitting diodes

Jialong Zhao; Jingying Zhang; Chaoyang Jiang; Jolanta Bohnenberger; Thomas Basché; Alf Mews

Electro- and photoluminescence spectra of the CdSe∕ZnS core-shell quantum dots (QDs) covered by various organic ligands and incorporated into multilayered light-emitting diodes (LEDs) were recorded by a confocal optical microscope. The QDs were dispersed in a hole transporting material, N,N’-Diphenyl-N,N’-bis(3-methylphenyl)-1,1’-biphenyl-4,4’-diamine (TPD), to investigate the LED performance at different QD concentrations and the effect of different surface modifications on the isolated QDs. No wavelength shift was observed in the electroluminescence spectra from the QD LEDs with or without the TPD. The peak energies of the electro- and photoluminescence showed only small spectral shifts (several nanometer) for the diluted QDs and no dependence on the QD-concentration, surface ligands, or conductive polymers that were used. This suggests that the relative peak shifts are related to the different filling processes in the CdSe QDs under photo excitation and electric injection, rather than to the “chemical”...


Applied Physics Letters | 2004

Photoelectronic transport imaging of individual semiconducting carbon nanotubes

Kannan Balasubramanian; Yuwei Fan; Marko Burghard; Klaus Kern; Marcel Friedrich; Uli Wannek; Alf Mews

Photoconductivity in individual semiconducting single-wall carbon nanotubes was investigated using a confocal scanning optical microscope. The magnitude of the photocurrent was found to increase linearly with the laser intensity, and to be maximum for parallel orientation between the light polarization and the tube axis. Larger currents were obtained upon illuminating the tubes at 514.5 nm in comparison to those at 647.1 nm, consistent with the semiconducting tubes having a resonant absorption energy at the former wavelength. Moreover, the determination of the photoresponse as a function of position along single nanotubes has proven to be a useful tool to monitor local electronic structure effects.


Nano Letters | 2010

Fluorescence Enhancement, Blinking Suppression, and Gray States of Individual Semiconductor Nanocrystals Close to Gold Nanoparticles

Xuedan Ma; Hua Tan; Tobias Kipp; Alf Mews

The optical properties of nanocrystals are drastically changed by the interaction with adjacent metal nanoparticles. By time-resolved photoluminescence spectroscopy, we investigate CdSe multishell nanocrystals coupled to self-assembled films of Au nanoparticles. The distance between emitter and metal is adjusted by coating the nanocrystals with silica shells. These NCs showed increased fluorescence intensity, a decreased fluorescence lifetime, strong blinking suppression, and fluorescence from gray states. These observations can be explained by the metal particle induced change of excitation and recombination rates.


Small | 2008

Formation and Function of Bismuth Nanocatalysts for the Solution–Liquid–Solid Synthesis of CdSe Nanowires

Zhen Li; Andreas Kornowski; Anton Myalitsin; Alf Mews

Small Bi nanoparticles prepared upon reduction of Bi-III compounds catalyze the growth of thick CdSe nanowires (see image). The control of Bi particle and CdSe nanowire growth rate allows adjustment of the dimensions of the nanowires, which is important for the preparation of various types of nanowires in solution.


Chemical Physics | 1999

TERRYLENE IN P-TERPHENYL : SINGLE-MOLECULE EXPERIMENTS AT ROOM TEMPERATURE

F. Kulzer; Felix Koberling; Th. Christ; Alf Mews; Th. Basché

Abstract This paper reports on fluorescence microscopy and spectroscopy of single terrylene molecules embedded in p -terphenyl at room temperature. The basic photophysical parameters of this crystalline host/guest system such as photostability, single-molecule emission rates and the properties of dispersed fluorescence spectra are reported. The stability of the single-molecule signals allowed the direct observation of singlet–triplet quantum jumps at room temperature, by means of which the underlying intersystem crossing rates can be investigated. The results of earlier investigations at liquid-helium temperatures are reviewed briefly where appropriate. The properties of terrylene in p -terphenyl are also compared to those of other host/guest systems at room temperature.


Nano Letters | 2010

Optical Modes Excited by Evanescent-Wave-Coupled PbS Nanocrystals in Semiconductor Microtube Bottle Resonators

Kay Dietrich; Christian Strelow; Constanze Schliehe; Christian Heyn; A. Stemmann; Stephan Schwaiger; Stefan Mendach; Alf Mews; Horst Weller; D. Heitmann; Tobias Kipp

We report on optical modes in rolled-up microtube resonators that are excited by PbS nanocrystals filled into the microtube core. Long ranging evanescent fields into the very thin walled microtubes cause strong emission of the nanocrystals into the resonator modes and a mode shift after a self-removal of the solvent. We present a method to precisely control the number, the energy and the localization of the modes along the microtube axis.


Nano Letters | 2011

Laser-induced charge separation in CdSe nanowires.

Sebastian Schäfer; Zhe Wang; Robert Zierold; Tobias Kipp; Alf Mews

A combination of electrostatic force microscopy and optical microscopy was used to investigate the charge state of individual CdSe nanowires upon local illumination with a focused laser beam. The nanowires were found to be positively charged at the excitation spot and negatively charged at the distant end(s). For high laser powers, the amount of accumulated charges increases logarithmically with the laser power. These effects are described by a diffusion-based model where the results are in good agreement with the experimentally observed effects. On the basis of this model the charge imbalance along the nanowire should establish in the course of nanoseconds. The net charge separation within homogeneous nanowires upon local illumination is of importance for several electronic devices.


ACS Nano | 2011

Diameter scaling of the optical band gap in individual CdSe nanowires.

Anton Myalitsin; Christian Strelow; Zhe Wang; Zhen Li; Tobias Kipp; Alf Mews

The diameter dependence of the optical band gap of single CdSe nanowires (NWs) is investigated by a combination of atomic force microscopy, scanning fluorescence microscopy, and transmission electron microscopy. We find a good congruence of the experimental data to calculations within the effective mass approximation taking into account quantization, exciton Coulomb interaction, and dielectric mismatch. The experimental data are furthermore compared to different theoretical approaches. We discuss the influence of alternating wurtzite and zinc blende segments along the NWs on their optical properties.


Journal of the American Chemical Society | 2015

Insight into Strain Effects on Band Alignment Shifts, Carrier Localization and Recombination Kinetics in CdTe/CdS Core/Shell Quantum Dots

Lihong Jing; Stephen V. Kershaw; Tobias Kipp; Sergii Kalytchuk; Ke Ding; Jianfeng Zeng; Mingxia Jiao; Xiaoyu Sun; Alf Mews; Andrey L. Rogach; Mingyuan Gao

The impact of strain on the optical properties of semiconductor quantum dots (QDs) is fundamentally important while still awaiting detailed investigation. CdTe/CdS core/shell QDs represent a typical strained system due to the substantial lattice mismatch between CdTe and CdS. To probe the strain-related effects, aqueous CdTe/CdS QDs were synthesized by coating different sized CdTe QD cores with CdS shells upon the thermal decomposition of glutathione as a sulfur source under reflux. The shell growth was carefully monitored by both steady-state absorption and fluorescence spectroscopy and transient fluorescence spectroscopy. In combination with structural analysis, the band alignments as a consequence of the strain were modified based on band deformation potential theory. By further taking account of these strain-induced band shifts, the effective mass approximation (EMA) model was modified to simulate the electronic structure, carrier spatial localization, and electron-hole wave function overlap for comparing with experimentally derived results. In particular, the electron/hole eigen energies were predicted for a range of structures with different CdTe core sizes and different CdS shell thicknesses. The overlap of electron and hole wave functions was further simulated to reveal the impact of strain on the electron-hole recombination kinetics as the electron wave function progressively shifts into the CdS shell region while the hole wave function remains heavily localized in CdTe core upon the shell growth. The excellent agreement between the strain-modified EMA model with the experimental data suggests that strain exhibits remarkable effects on the optical properties of mismatched core/shell QDs by altering the electronic structure of the system.

Collaboration


Dive into the Alf Mews's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Zhe Wang

University of Hamburg

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Xuedan Ma

University of Hamburg

View shared research outputs
Researchain Logo
Decentralizing Knowledge