TY - JOUR AB - Metallic nanoparticles co-functionalised with monolayers of UV- and CO2-sensitive ligands were prepared and shown to respond to these two types of stimuli reversibly and in an orthogonal fashion. The composition of the coating could be tailored to yield nanoparticles capable of aggregating exclusively when both UV and CO2 were applied at the same time, analogously to the behaviour of an AND logic gate. AU - Lee, Ji-Woong AU - Klajn, Rafal ID - 13395 IS - 11 JF - Chemical Communications KW - Materials Chemistry KW - Metals and Alloys KW - Surfaces KW - Coatings and Films KW - General Chemistry KW - Ceramics and Composites KW - Electronic KW - Optical and Magnetic Materials KW - Catalysis SN - 1359-7345 TI - Dual-responsive nanoparticles that aggregate under the simultaneous action of light and CO2 VL - 51 ER - TY - JOUR AB - Photoswitching in densely packed azobenzene self-assembled monolayers (SAMs) is strongly affected by steric constraints and excitonic coupling between neighboring chromophores. Therefore, control of the chromophore density is essential for enhancing and manipulating the photoisomerization yield. We systematically compare two methods to achieve this goal: First, we assemble monocomponent azobenzene–alkanethiolate SAMs on gold nanoparticles of varying size. Second, we form mixed SAMs of azobenzene–alkanethiolates and “dummy” alkanethiolates on planar substrates. Both methods lead to a gradual decrease of the chromophore density and enable efficient photoswitching with low-power light sources. X-ray spectroscopy reveals that coadsorption from solution yields mixtures with tunable composition. The orientation of the chromophores with respect to the surface normal changes from a tilted to an upright position with increasing azobenzene density. For both systems, optical spectroscopy reveals a pronounced excitonic shift that increases with the chromophore density. In spite of exciting the optical transition of the monomer, the main spectral change in mixed SAMs occurs in the excitonic band. In addition, the photoisomerization yield decreases only slightly by increasing the azobenzene–alkanethiolate density, and we observed photoswitching even with minor dilutions. Unlike in solution, azobenzene in the planar SAM can be switched back almost completely by optical excitation from the cis to the original trans state within a short time scale. These observations indicate cooperativity in the photoswitching process of mixed SAMs. AU - Moldt, Thomas AU - Brete, Daniel AU - Przyrembel, Daniel AU - Das, Sanjib AU - Goldman, Joel R. AU - Kundu, Pintu K. AU - Gahl, Cornelius AU - Klajn, Rafal AU - Weinelt, Martin ID - 13396 IS - 3 JF - Langmuir KW - Electrochemistry KW - Spectroscopy KW - Surfaces and Interfaces KW - Condensed Matter Physics KW - General Materials Science SN - 0743-7463 TI - Tailoring the properties of surface-immobilized azobenzenes by monolayer dilution and surface curvature VL - 31 ER - TY - JOUR AB - Self-assembly of inorganic nanoparticles has been studied extensively for particles having different sizes and compositions. However, relatively little attention has been devoted to how the shape and surface chemistry of magnetic nanoparticles affects their self-assembly properties. Here, we undertook a combined experiment–theory study aimed at better understanding of the self-assembly of cubic magnetite (Fe3O4) particles. We demonstrated that, depending on the experimental parameters, such as the direction of the magnetic field and nanoparticle density, a variety of superstructures can be obtained, including one-dimensional filaments and helices, as well as C-shaped assemblies described here for the first time. Furthermore, we functionalized the surfaces of the magnetic nanocubes with light-sensitive ligands. Using these modified nanoparticles, we were able to achieve orthogonal control of self-assembly using a magnetic field and light. AU - Singh, Gurvinder AU - Chan, Henry AU - Udayabhaskararao, T. AU - Gelman, Elijah AU - Peddis, Davide AU - Baskin, Artem AU - Leitus, Gregory AU - Král, Petr AU - Klajn, Rafal ID - 13397 JF - Faraday Discussions KW - Physical and Theoretical Chemistry SN - 1359-6640 TI - Magnetic field-induced self-assembly of iron oxide nanocubes VL - 181 ER - TY - JOUR AU - Sun, Yugang AU - Scarabelli, Leonardo AU - Kotov, Nicholas AU - Tebbe, Moritz AU - Lin, Xiao-Min AU - Brullot, Ward AU - Isa, Lucio AU - Schurtenberger, Peter AU - Moehwald, Helmuth AU - Fedin, Igor AU - Velev, Orlin AU - Faivre, Damien AU - Sorensen, Christopher AU - Perzynski, Régine AU - Chanana, Munish AU - Li, Zhihai AU - Bresme, Fernando AU - Král, Petr AU - Firlar, Emre AU - Schiffrin, David AU - Souza Junior, Joao Batista AU - Fery, Andreas AU - Shevchenko, Elena AU - Tarhan, Ozgur AU - Alivisatos, Armand Paul AU - Disch, Sabrina AU - Klajn, Rafal AU - Ghosh, Suvojit ID - 13398 JF - Faraday Discussions KW - Physical and Theoretical Chemistry SN - 1359-6640 TI - Field-assisted self-assembly process: General discussion VL - 181 ER - TY - JOUR AB - The detection of electron motion and electronic wave-packet dynamics is one of the core goals of attosecond science. Recently, choosing the nitric oxide molecule as an example, we have introduced and demonstrated an experimental approach to measure coupled valence electronic and rotational wave packets using high-order-harmonic-generation (HHG) spectroscopy [Kraus et al., Phys. Rev. Lett. 111, 243005 (2013)]. A short outline of the theory to describe the combination of the pump and HHG probe process was published together with an extensive discussion of experimental results [Baykusheva et al., Faraday Discuss. 171, 113 (2014)]. The comparison of theory and experiment showed good agreement on a quantitative level. Here, we present the theory in detail, which is based on a generalized density-matrix approach that describes the pump process and the subsequent probing of the wave packets by a semiclassical quantitative rescattering approach. An in-depth analysis of the different Raman scattering contributions to the creation of the coupled rotational and electronic spin-orbit wave packets is made. We present results for parallel and perpendicular linear polarizations of the pump and probe laser pulses. Furthermore, an analysis of the combined rotational-electronic density matrix in terms of irreducible components is presented that facilitates interpretation of the results. AU - Zhang, Song Bin AU - Baykusheva, Denitsa Rangelova AU - Kraus, Peter M. AU - Wörner, Hans Jakob AU - Rohringer, Nina ID - 14017 IS - 2 JF - Physical Review A KW - Atomic and Molecular Physics KW - and Optics SN - 1050-2947 TI - Theoretical study of molecular electronic and rotational coherences by high-order-harmonic generation VL - 91 ER -