• Energy Research
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AbstractLichtablenkungseffekte können bei der interferometrischen Beobachtung von Grenzschichten zu großen Fehlern bei der Ableitung der Konzentrationsprofile führen, sofern nicht Korrekturen bei der Interpretation vorgenommen werden.

AbstractGold, silver, platinum and palladium typically crystallize with the face-centred cubic structure. Here we report the high-yield solution synthesis of gold nanoribbons in the 4H hexagonal polytype, a previously unreported metastable phase of gold. These gold nanoribbons undergo a phase transition from the original 4H hexagonal to face-centred cubic structure on ligand exchange under ambient conditions. Using monochromated electron energy-loss spectroscopy, the strong infrared plasmon absorption of single 4H gold nanoribbons is observed. Furthermore, the 4H hexagonal phases of silver, palladium and platinum can be readily stabilized through direct epitaxial growth of these metals on the 4H gold nanoribbon surface. Our findings may open up new strategies for the crystal phase-controlled synthesis of advanced noble metal nanomaterials.

A controllable planar Fe2O3/WO3 photoanode with an integrated Co(OH)x layer was prepared via an electrospray technique for enhanced PEC performance.

The oxidation of water is essential to the sustainable production of fuels using sunlight or electricity, but designing active, stable and earth-abundant catalysts for the reaction is challenging. Now, a complex containing five iron atoms is shown to efficiently oxidize water by mimicking key features of the oxygen-evolving complex in green plants.

For lithium–sulfur batteries, 3D cathodes might be of interest for containing the active material and trapping the polysulfides during cycling, owing to their binder-free and freestanding features. In this work, the MoS2 grown on the 3D structured Carbon Cloth (CC@MoS2) is firstly used to fabricate the Li–S battery and the sulfur loading can be freely tuned by adjusting thermal annealing time at 200 °C. A two-step melt-diffusion strategy is reported for fabrication of cathodes, which involves in melting and diffusion of sulfur covered by CC@MoS2 composites instead of dissolution of sulfur in the toxic organic solvents. Compared with the non-polar carbon cloth, the CC@MoS2 composites exhibit better adsorption capacity for polysulfides due to more edge active sites, which could effectively facilitate polysulfide redox kinetics. The SEM images of the CC@MoS2 cathode after 300 cycles show that MoS2 can still maintain the nanosheet morphology. After 300 cycles at 0.5 C, the CC@MoS2 cathodes loaded with 2 mg sulfur exhibit a better reversible capacity of 698 mA h g−1 compared with CC@MoS2 loaded with 1 mg sulfur (604 mA h g−1) and CC@MoS2 loaded with 4 mg sulfur (420 mA h g−1). This work proposes an environmentally friendly method to fabricate the lithium–sulfur battery cathode material and the sulfur loading can be freely adjusted.

Conventional circular double or triple tube type heat exchanger, DHE or THE, is one of the compact heat exchangers; a large number of studies have been performed to improve their heat transfer performance. The authors demonstrated that a petal-shaped special DHE with a large wet perimeter yields a high heat transfer efficiency, η. In this study, the DHE with six or five petals-, five shallow petals-, and circular-inner tubes were used. To further improve the η of the DHE, a THE with a petal-shaped inner tube along with the middle and outer circular tubes were used. Hot water flowed through the inner tube and cold water flowed through the middle and outer tubes as a counter current flow. The heat transfer was approximately equal; however, the flow resistance (pressure loss) of the outer tube of the DHE could be decreased using the middle and outer tubes under the same amount of cold water as the DHE; consequently, the η could be improved. In addition, the effect of changing the flow path of the hot- and cold-water flows on the η was examined.

AbstractAn eco‐friendly and sustainable salt‐templating approach was proposed for the production of anode materials with a 3D sponge‐like structure for sodium‐ion capacitors using gluconic acid as carbon precursor and sodium carbonate as water‐removable template. The optimized carbon material combined porous thin walls that provided short diffusional paths, a highly disordered microstructure with dilated interlayer spacing, and a large oxygen content, all of which facilitated Na ion transport and provided plenty of active sites for Na adsorption. This material provided a capacity of 314 mAh g−1 at 0.1 A g−1 and 130 mAh g−1 at 10 A g−1. When combined with a 3D highly porous carbon cathode (SBET ≈2300 m2 g−1) synthesized from the same precursor, the Na‐ion capacitor showed high specific energy/power, that is 110 Wh kg−1 at low power and still 71 Wh kg−1 at approximately 26 kW kg−1, and a good capacity retention of 70 % over 10000 cycles.

AbstractThe functionalization and application of nano‐objects generated using a polymerization induced self‐assembly (PISA) procedure is becoming a focus in recent years. In this contribution, using ethanol as solvent, poly(oligo(ethylene oxide) methyl ether methacrylate) (POEOMA) as macro‐initiator/stabilizer, and 2‐(perfluorohexyl)ethyl methacrylate (PFHEMA) and glycidyl methacrylate (GMA) as comonomers, the initiators for continuous activator regeneration atom transfer radical polymerization (ICAR ATRP)‐based PISA is realized. The lower GMA content system tends to form spheres with large diameters and heavy contrast, while the lower PFHEMA content system tends to form the spheres or short worms with small diameters. However, the system with further increased GMA content results in the failed ICAR ATRP PISA procedure with the formation of precipitates by the cross‐linking reaction between pendant epoxy groups. Furthermore, using the efficient reaction between the epoxy group on GMA and thiol group on mercapto‐succinic acid agent, the carboxyl groups can be introduced into the inner cavity of the nano‐objects and used for incorporation with the Fe2+ and Fe3+ ions, and the organic–inorganic nanoparticles Fe3O4@POEOMA are finally prepared in the presence of a reductant.