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- ItemA Highly Active Cobalt Catalyst for the General and Selective Hydrogenation of Aromatic Heterocycles(Weinheim : Wiley-VCH, 2023) Bauer, Christof; Müller, Felix; Keskin, Sercan; Zobel, Mirijam; Kempe, RhettNanostructured earth abundant metal catalysts that mediate important chemical reactions with high efficiency and selectivity are of great interest. This study introduces a synthesis protocol for nanostructured earth abundant metal catalysts. Three components, an inexpensive metal precursor, an easy to synthesize N/C precursor, and a porous support material undergo pyrolysis to give the catalyst material in a simple, single synthesis step. By applying this catalyst synthesis, a highly active cobalt catalyst for the general and selective hydrogenation of aromatic heterocycles could be generated. The reaction is important with regard to organic synthesis and hydrogen storage. The mild reaction conditions observed for quinolines permit the selective hydrogenation of numerous classes of N-, O- and S-heterocyclic compounds such as: quinoxalines, pyridines, pyrroles, indoles, isoquinoline, aciridine amine, phenanthroline, benzofuranes, and benzothiophenes.
- ItemInfluence of Nanoparticle Processing on the Thermoelectric Properties of (BixSb1−X)2Te3 Ternary Alloys(Weinheim : Wiley-VCH, 2021) Salloum, Sarah; Bendt, Georg; Heidelmann, Markus; Loza, Kateryna; Bayesteh, Samaneh; Izadi, M. Sepideh; Patrick, Kawulok; He, Ran; Schlörb, Heike; Perez, Nicolas; Reith, Heiko; Nielsch, Kornelius; Schierning, Gabi; Schulz, StephanThe synthesis of phase‐pure ternary solutions of tetradymite‐type materials (BixSb1−x)2Te3 (x=0.25; 0.50; 0.75) in an ionic liquid approach has been carried out. The nanoparticles are characterized by means of energy‐dispersive X‐ray spectroscopy (EDX), powder X‐ray diffraction (PXRD), scanning electron microscopy (SEM), and transmission electron microscopy. In addition, the role of different processing approaches on the thermoelectric properties ‐ Seebeck coefficient as well as electrical and thermal conductivity ‐ is demonstrated.
- ItemLight-Driven Proton Transfer for Cyclic and Temporal Switching of Enzymatic Nanoreactors(Weinheim : Wiley-VCH, 2020) Moreno, Silvia; Sharan, Priyanka; Engelke, Johanna; Gumz, Hannes; Boye, Susanne; Oertel, Ulrich; Wang, Peng; Banerjee, Susanta; Klajn, Rafal; Voit, Brigitte; Lederer, Albena; Appelhans, DietmarTemporal activation of biological processes by visible light and subsequent return to an inactive state in the absence of light is an essential characteristic of photoreceptor cells. Inspired by these phenomena, light-responsive materials are very attractive due to the high spatiotemporal control of light irradiation, with light being able to precisely orchestrate processes repeatedly over many cycles. Herein, it is reported that light-driven proton transfer triggered by a merocyanine-based photoacid can be used to modulate the permeability of pH-responsive polymersomes through cyclic, temporally controlled protonation and deprotonation of the polymersome membrane. The membranes can undergo repeated light-driven swelling-contraction cycles without losing functional effectiveness. When applied to enzyme loaded-nanoreactors, this membrane responsiveness is used for the reversible control of enzymatic reactions. This combination of the merocyanine-based photoacid and pH-switchable nanoreactors results in rapidly responding and versatile supramolecular systems successfully used to switch enzymatic reactions ON and OFF on demand.
- ItemPhotocatalytic Reduction of CO2 by Metal-Free-Based Materials: Recent Advances and Future Perspective(Weinheim : Wiley-VCH, 2020) Shen, Huidong; Peppel, Tim; Strunk, Jennifer; Sun, ZhenyuPhotocatalytic CO2 reduction to produce valuable chemicals and fuels using solar energy provides an appealing route to alleviate global energy and environmental problems. Searching for photocatalysts with high activity and selectivity for CO2 conversion is the key to achieving this goal. Among the various proposed photocatalysts, metal-free materials, such as graphene, nitrides, carbides, and conjugated organic polymers, have gained extensive research interest for photocatalytic CO2 reduction, due to their earth abundance, cost-effectiveness, good electrical conductivity, and environmental friendliness. They exhibit prominent catalytic activity, impressive selectivity, and long durability for the conversion of CO2 to solar fuels. Herein, the recent progress on metal-free photocatalysis of CO2 reduction is systematically reviewed. Opportunities and challenges on modification of nonmetallic catalysts to enhance CO2 transformation are presented. Theoretical calculations on possible reduction mechanisms and pathways as well as the potential in situ and operando techniques for mechanistic understanding are also summarized and discussed. Based on the aforementioned discussions, suitable future research directions and perspectives for the design and development of potential nonmetallic photocatalysts for efficient CO2 reduction are provided. © 2020 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
- ItemLong-Living Holes in Grey Anatase TiO2 Enable Noble-Metal-Free and Sacrificial-Agent-Free Water Splitting(Weinheim : Wiley-VCH, 2020) Liu, Ning; Mohajernia, Shiva; Nguyen, Nhat Truong; Hejazi, Seyedsina; Plass, Fabian; Kahnt, Axel; Yokosawa, Tadahiro; Osvet, Andres; Spiecker, Erdmann; Guldi, Dirk M.; Schmuki, PatrikTitanium dioxide has been the benchmark semiconductor in photocatalysis for more than 40 years. Full water splitting, that is, decomposing water into H2 and O2 in stoichiometric amounts and with an acceptable activity, still remains a challenge, even when TiO2-based photocatalysts are used in combination with noble-metal co-catalysts. The bottleneck of anatase-type TiO2 remains the water oxidation, that is, the hole transfer reaction from pristine anatase to the aqueous environment. In this work, we report that “grey” (defect engineered) anatase can provide a drastically enhanced lifetime of photogenerated holes, which, in turn, enables an efficient oxidation reaction of water to peroxide via a two-electron pathway. As a result, a Ni@grey anatase TiO2 catalyst can be constructed with an impressive performance in terms of photocatalytic splitting of neutral water into H2 and a stoichiometric amount of H2O2 without the need of any noble metals or sacrificial agents. The finding of long hole lifetimes in grey anatase opens up a wide spectrum of further photocatalytic applications of this material. © 2020 The Authors. Published by Wiley-VCH GmbH
- ItemSimultaneous Effect of Ultraviolet Radiation and Surface Modification on the Work Function and Hole Injection Properties of ZnO Thin Films(Weinheim : Wiley-VCH, 2020) Raoufi, Meysam; Hörmann, Ulrich; Ligorio, Giovanni; Hildebrandt, Jana; Pätzel, Michael; Schultz, Thorsten; Perdigon, Lorena; Koch, Norbert; List-Kratochvil, Emil; Hecht, Stefan; Neher, DieterThe combined effect of ultraviolet (UV) light soaking and self-assembled monolayer deposition on the work function (WF) of thin ZnO layers and on the efficiency of hole injection into the prototypical conjugated polymer poly(3-hexylthiophen-2,5-diyl) (P3HT) is systematically investigated. It is shown that the WF and injection efficiency depend strongly on the history of UV light exposure. Proper treatment of the ZnO layer enables ohmic hole injection into P3HT, demonstrating ZnO as a potential anode material for organic optoelectronic devices. The results also suggest that valid conclusions on the energy-level alignment at the ZnO/organic interfaces may only be drawn if the illumination history is precisely known and controlled. This is inherently problematic when comparing electronic data from ultraviolet photoelectron spectroscopy (UPS) measurements carried out under different or ill-defined illumination conditions. © 2020 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
- ItemTemperature-Dependent Charge Carrier Diffusion in [0001¯] Direction of GaN Determined by Luminescence Evaluation of Buried InGaN Quantum Wells(Weinheim : Wiley-VCH, 2020) Netzel, Carsten; Hoffmann, Veit; Tomm, Jens W.; Mahler, Felix; Einfeldt, Sven; Weyers, MarkusTemperature-dependent transport of photoexcited charge carriers through a nominally undoped, c-plane GaN layer toward buried InGaN quantum wells is investigated by continuous-wave and time-resolved photoluminescence spectroscopy. The excitation of the buried InGaN quantum wells is dominated by charge carrier diffusion through the GaN layer; photon recycling contributes only slightly. With temperature decreasing from 310 to 10 K, the diffusion length in [0001⎯⎯] direction increases from 250 to 600 nm in the GaN layer. The diffusion length at 300 K also increases from 100 to 300 nm when increasing the excitation power density from 20 to 500 W cm−2. The diffusion constant decreases from the low-temperature value of ∼7 to 1.5 cm2 s−1 at 310 K. The temperature dependence of the diffusion constant indicates that the diffusivity at room temperature is limited by optical phonon scattering. Consequently, higher diffusion constants in GaN-based devices require a reduced operation temperature. To increase diffusion lengths at a fixed temperature, the effective recombination time has to be prolonged by reducing the number of nonradiative recombination centers.
- ItemAll-Conjugated Polymer Core-Shell and Core-Shell-Shell Particles with Tunable Emission Profiles and White Light Emission(Weinheim : Wiley-VCH, 2021) Haehnle, Bastian; Schuster, Philipp A.; Chen, Lisa; Kuehne, Alexander J. C.Future applications of conjugated polymer particles (CPP) in medicine, organic photonics, and optoelectronics greatly depend on high performance and precisely adjustable optical properties of the particles. To meet these criteria, current particle systems often combine conjugated polymers with inorganic particles in core-shell geometries, extending the possible optical characteristics of CPP. However, current conjugated polymer particles are restricted to a single polymer phase composed of a distinct polymer or a polymer blend. Here, a synthetic toolbox is presented that enables the synthesis of monodisperse core-shell and core-shell-shell particles, which consist entirely of conjugated polymers but of different types in the core and the shells. Seeded and fed-batch dispersion polymerizations based on Suzuki-Miyaura-type cross-coupling are investigated. The different approaches allow accurate control over the created interface between the conjugated polymer phases and thus also over the energy transfer phenomena between them. This approach opens up completely new synthetic freedom for fine tuning of the optical properties of CPP, enabling, for example, the synthesis of individual white light-emitting particles.
- ItemNanostructured Silicon Matrix for Materials Engineering(Weinheim : Wiley-VCH, 2023) Liu, Poting; Schleusener, Alexander; Zieger, Gabriel; Bochmann, Arne; van Spronsen, Matthijs A.; Sivakov, VladimirTin-containing layers with different degrees of oxidation are uniformly distributed along the length of silicon nanowires formed by a top-down method by applying metalorganic chemical vapor deposition. The electronic and atomic structure of the obtained layers is investigated by applying nondestructive surface-sensitive X-ray absorption near edge spectroscopy using synchrotron radiation. The results demonstrated, for the first time, a distribution effect of the tin-containing phases in the nanostructured silicon matrix compared to the results obtained for planar structures at the same deposition temperatures. The amount and distribution of tin-containing phases can be effectively varied and controlled by adjusting the geometric parameters (pore diameter and length) of the initial matrix of nanostructured silicon. Due to the occurrence of intense interactions between precursor molecules and decomposition by-products in the nanocapillary, as a consequence of random thermal motion of molecules in the nanocapillary, which leads to additional kinetic energy and formation of reducing agents, resulting in effective reduction of tin-based compounds to a metallic tin state for molecules with the highest penetration depth in the nanostructured silicon matrix. This effect will enable clear control of the phase distributions of functional materials in 3D matrices for a wide range of applications.
- ItemSelf-Activation of Inorganic-Organic Hybrids Derived through Continuous Synthesis of Polyoxomolybdate and para-Phenylenediamine Enables Very High Lithium-Ion Storage Capacity(Weinheim : Wiley-VCH, 2023) Mohamed, Mana Abdirahman; Arnold, Stefanie; Janka, Oliver; Quade, Antje; Presser, Volker; Kickelbick, GuidoInorganic-organic hybrid materials with redox-active components were prepared by an aqueous precipitation reaction of ammonium heptamolybdate (AHM) with para-phenylenediamine (PPD). A scalable and low-energy continuous wet chemical synthesis process, known as the microjet process, was used to prepare particles with large surface area in the submicrometer range with high purity and reproducibility on a large scale. Two different crystalline hybrid products were formed depending on the ratio of molybdate to organic ligand and pH. A ratio of para-phenylenediamine to ammonium heptamolybdate from 1 : 1 to 5 : 1 resulted in the compound [C6H10N2]2[Mo8O26] ⋅ 6 H2O, while higher PPD ratios from 9 : 1 to 30 : 1 yielded a composition of [C6H9N2]4[NH4]2[Mo7O24] ⋅ 3 H2O. The electrochemical behavior of the two products was tested in a battery cell environment. Only the second of the two hybrid materials showed an exceptionally high capacity of 1084 mAh g−1 at 100 mA g−1 after 150 cycles. The maximum capacity was reached after an induction phase, which can be explained by a combination of a conversion reaction with lithium to Li2MoO4 and an additional in situ polymerization of PPD. The final hybrid material is a promising material for lithium-ion battery (LIB) applications.