k-space imaging of the eigenmodes of sharp gold tapers for scanning near-field optical microscopy

• Martin Esmann,
• Simon F. Becker,
• Bernard B. da Cunha,
• Jens H. Brauer,
• Ralf Vogelgesang,
• Petra Groß and
• Christoph Lienau

Beilstein J. Nanotechnol. 2013, 4, 603–610, doi:10.3762/bjnano.4.67

• silicon step edge [12] have been imaged, demonstrating an optical resolution of down to 10 nm. Moreover, time-resolved studies showed that the time structure of ultra-fast laser pulses in the few-femtosecond regime hardly changes upon grating coupling to SPPs and during propagation over distances of

Femtosecond-resolved ablation dynamics of Si in the near field of a small dielectric particle

• Paul Kühler,
• Daniel Puerto,
• Mario Mosbacher,
• Paul Leiderer,
• Francisco Javier Garcia de Abajo,
• Jan Siegel and
• Javier Solis

Beilstein J. Nanotechnol. 2013, 4, 501–509, doi:10.3762/bjnano.4.59

• span from 0.1 ps to about 1 ns. Characteristic phenomena like electron plasma formation, ultrafast melting and ablation, along with their characteristic time scales are observed in the region surrounding the particle. The use of a time resolved imaging technique allows us recording simultaneously the

• material response at ordinary and large peak power densities enabling a direct comparison between both scenarios. The time resolved images of near field exposed regions are consistent with a remarkable temporal shift of the ablation onset which occurs in the sub-picosend regime, from about 500 to 800 fs

• . Further details regarding the preparation procedure and optical properties of the different substrates and particles used, as well as near field imaging using GST films can be found elsewhere [11]. Femtosecond laser irradiation and time-resolved microscopy Figure 2 shows a scheme of the set-up used for

Kelvin probe force microscopy of nanocrystalline TiO₂ photoelectrodes

• Alex Henning,
• Gino Günzburger,
• Res Jöhr,
• Yossi Rosenwaks,
• Biljana Bozic-Weber,
• Catherine E. Housecroft,
• Edwin C. Constable,
• Ernst Meyer and
• Thilo Glatzel

Beilstein J. Nanotechnol. 2013, 4, 418–428, doi:10.3762/bjnano.4.49

• ., surface topography and potential, are still unclear and have the potential to increase the efficiency and long-term stability of the devices. Investigations of nanoscaled photovoltaic devices require nanometer-scale measuring methods, including time-resolved measurements of the carrier dynamics [15][16

• light, i.e., super- or sub-bandgap(TiO2) illumination. Both SPV effects are described separately in the following two sections. Time-resolved SPV measurements provide insights into charge carrier dynamics [45] and are described below. Surface photovoltage under super-bandgap illumination SPV

Near-field effects and energy transfer in hybrid metal-oxide nanostructures

• Ulrich Herr,
• Balati Kuerbanjiang,
• Cahit Benel,
• Giorgos Papageorgiou,
• Manuel Goncalves,
• Johannes Boneberg,
• Paul Leiderer,
• Paul Ziemann,
• Peter Marek and
• Horst Hahn

Beilstein J. Nanotechnol. 2013, 4, 306–317, doi:10.3762/bjnano.4.34

• about the excitation processes in the TiO2:Eu nanoparticles, we conducted time-resolved emission measurements using a xenon flash lamp for the excitation. Figure 5 shows the decay of the emission at 617 nm under excitation at 330 nm. We find that the decay of the emission under these conditions is

Photoresponse from single upright-standing ZnO nanorods explored by photoconductive AFM

• Igor Beinik,
• Markus Kratzer,
• Astrid Wachauer,
• Lin Wang,
• Yuri P. Piryatinski,
• Gerhard Brauer,
• Xin Yi Chen,
• Yuk Fan Hsu,
• Aleksandra B. Djurišić and
• Christian Teichert

Beilstein J. Nanotechnol. 2013, 4, 208–217, doi:10.3762/bjnano.4.21

• have also performed time-resolved photoluminescence measurements macroscopically. Results: Persistent photoconductivity from single ZnO NRs was observed for about 1800 s and was studied with the help of photocurrent spectroscopy, which was recorded locally. The photocurrent spectra recorded from single

• technique to study the electrical transport in individual upright standing ZnO NRs grown by thermal evaporation [41]. The results obtained together with those of time-resolved photoluminescence (PL) suggest that the photoresponse in ZnO NRs originates preferentially from the photoexcitation of charge

• macroscopically by means of time-resolved photoluminescence (TR-PL). The conventional steady-state PL and TR-PL were measured at 300 K. The monochromator used for both types of PL experiments has a linear dispersion of 0.8 nm/mm and was equipped with a photomultiplier tube as photodetector. The setup for the TR

Horizontal versus vertical charge and energy transfer in hybrid assemblies of semiconductor nanoparticles

• Gilad Gotesman,
• Rahamim Guliamov and
• Ron Naaman

Beilstein J. Nanotechnol. 2012, 3, 629–636, doi:10.3762/bjnano.3.72

• Gilad Gotesman Rahamim Guliamov Ron Naaman Department of Chemical Physics, The Weizmann Institute of Science, Rehovot 76100, Israel 10.3762/bjnano.3.72 Abstract We studied the photoluminescence and time-resolved photoluminescence from self-assembled bilayers of donor and acceptor nanoparticles

Direct monitoring of opto-mechanical switching of self-assembled monolayer films containing the azobenzene group

• Einat Tirosh,
• Enrico Benassi,
• Silvio Pipolo,
• Marcel Mayor,
• Michal Valášek,
• Veronica Frydman,
• Stefano Corni and
• Sidney R. Cohen

Beilstein J. Nanotechnol. 2011, 2, 834–844, doi:10.3762/bjnano.2.93

• and reliable referencing to the substrate must be made. The method applied here is time-resolved tapping force imaging, in which force–deformation curves are reconstructed from the amplitudes of the higher harmonics of oscillation of the flexural mode of the cantilever, spring-coupled to the torsional

Highly efficient ZnO/Au Schottky barrier dye-sensitized solar cells: Role of gold nanoparticles on the charge-transfer process

• Tanujjal Bora,
• Htet H. Kyaw,
• Soumik Sarkar,
• Samir K. Pal and
• Joydeep Dutta

Beilstein J. Nanotechnol. 2011, 2, 681–690, doi:10.3762/bjnano.2.73

• available picosecond diode laser-pumped (LifeSpec-ps) time-resolved fluorescence spectrophotometer from Edinburgh Instruments, U.K. Picosecond excitation pulses from the picoquant diode laser were used at 409 nm with an instrument response function (IRF) of 50 ps. A microchannel plate photomultiplier tube

Femtosecond time-resolved photodissociation dynamics of methyl halide molecules on ultrathin gold films

• Mihai E. Vaida,
• Robert Tchitnga and
• Thorsten M. Bernhardt

Beilstein J. Nanotechnol. 2011, 2, 618–627, doi:10.3762/bjnano.2.65

• present investigation focuses on fundamental mechanistic aspects associated with the interaction of small organic molecules with metal surfaces. For this purpose, ultrafast, time-resolved laser spectroscopy was applied to provide insight into light-induced molecular fragmentation on surfaces on the time

• has been reported so far about the adsorption of methyl bromide or methyl chloride on gold. Also, no ultrafast time-resolved laser investigations of methyl halide molecules on metal substrates have been performed so far. Only recently, the femtosecond (fs)-laser time-resolved photodissociation of

• free molecule [3] cannot be energetically lowered enough to become accessible to the 4.7 eV photons of the 266 nm pump laser beam. Conclusion The present investigation demonstrates that time resolved pump–probe fs-laser time-of-flight mass spectrometry is able to probe the photodissociation dynamics of

Nanostructured, mesoporous Au/TiO₂ model catalysts – structure, stability and catalytic properties

• Matthias Roos,
• Dominique Böcking,
• Kwabena Offeh Gyimah,
• Gabriela Kucerova,
• Joachim Bansmann,
• Johannes Biskupek,
• Ute Kaiser,
• Nicola Hüsing and
• R. Jürgen Behm

Beilstein J. Nanotechnol. 2011, 2, 593–606, doi:10.3762/bjnano.2.63

• room temperature, and in particular on ii) exploring the role of transport effects in these films on the reaction characteristics, both by locally resolved measurements on microstructured samples by means of higher resolution scanning mass spectrometry and by time-resolved measurements, e.g., in a

Characterization of protein adsorption onto FePt nanoparticles using dual-focus fluorescence correlation spectroscopy

• Pauline Maffre,
• Karin Nienhaus,
• Faheem Amin,
• Wolfgang J. Parak and
• G. Ulrich Nienhaus

Beilstein J. Nanotechnol. 2011, 2, 374–383, doi:10.3762/bjnano.2.43

• thickness on these NPs, and time-resolved fluorescence quenching experiments revealed a typical protein residence time of ~100 s [11]. For transferrin [8], an important blood plasma protein involved in iron transport and delivery, we observed formation of a 7 nm thick protein corona. The FCS method is based

• . 2fFCS setup The 2fFCS setup is based on a time-resolved confocal microscopy system (Microtime 200, PicoQuant, Berlin, Germany). Instead of using a single excitation laser, the light from two identical, orthogonally polarized pulsed 640 nm diode lasers (LDH-P-C-640B, Picoquant, Berlin, Germany) was

Intermolecular vs molecule–substrate interactions: A combined STM and theoretical study of supramolecular phases on graphene/Ru(0001)

• Michael Roos,
• Benedikt Uhl,
• Daniela Künzel,
• Harry E. Hoster,
• Axel Groß and
• R. Jürgen Behm

Beilstein J. Nanotechnol. 2011, 2, 365–373, doi:10.3762/bjnano.2.42

• nm); The same hydrogen bonding configuration and hexagonal network, but without spacing between the hexagons. (d) Model of 3,3'-BTP on HOPG. Each molecule shares two hydrogen bonds with its adjacent hexagon (yellow ellipses). Sequence of time resolved images recorded at 2 fps showing every 10th image

Sensing surface PEGylation with microcantilevers

• Natalija Backmann,
• Natascha Kappeler,
• Thomas Braun,
• François Huber,
• Hans-Peter Lang,
• Christoph Gerber and
• Roderick Y. H. Lim

Beilstein J. Nanotechnol. 2010, 1, 3–13, doi:10.3762/bjnano.1.2

• , time resolved manner [13][14]. By an asymmetrical chemisorption of molecules (i.e., on one side of the microcantilever), the sensors can detect processes in “static” mode by measuring the bending of a microcantilever due to stress formation during the adsorption process; or in “dynamic” mode where the