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Earth-abundant photocatalytic systems for the visible-light-driven reduction of CO2 to CO

2017, Rosas-Hernández, Alonso, Steinlechner, Christoph, Junge, Henrik, Beller, Matthias

Herein, we report a highly selective photocatalytic system, based on an in situ copper photosensitizer and an iron catalyst, for the reduction of CO2 to CO. Turnover numbers (TON) up to 487 (5 h) with selectivities up to 99% and ΦCO = 13.3% were observed. Stern-Volmer analysis allowed us to establish a reductive quenching mechanism between the Cu PS and electron donor.

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Covalency and vibronic couplings make a nonmagnetic j=3/2 ion magnetic

2016, Xu, Lei, Bogdanov, Nikolay A., Princep, Andrew, Fulde, Peter, van den Brink, Jeroen, Hozoi, Liviu

For 4d1 and 5d1 spin–orbit-coupled electron configurations, the notion of nonmagnetic j=3/2 quartet ground state discussed in classical textbooks is at odds with the observed variety of magnetic properties. Here we throw fresh light on the electronic structure of 4d1 and 5d1 ions in molybdenum- and osmium-based double-perovskite systems and reveal different kinds of on-site many-body physics in the two families of compounds: although the sizable magnetic moments and g-factors measured experimentally are due to both metal d–ligand p hybridisation and dynamic Jahn–Teller interactions for 4d electrons, it is essentially d−p covalency for the 5d1 configuration. These results highlight the subtle interplay of spin–orbit interactions, covalency and electron–lattice couplings as the major factor in deciding the nature of the magnetic ground states of 4d and 5d quantum materials. Cation charge imbalance in the double-perovskite structure is further shown to allow a fine tuning of the gap between the t2g and eg levels, an effect of much potential in the context of orbital engineering in oxide electronics.

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Hydrogenation of terminal and internal olefins using a biowaste-derived heterogeneous cobalt catalyst

2018, Scharnagl, Florian Korbinian, Hertrich, Maximilian Franz, Ferretti, Francesco, Kreyenschulte, Carsten, Lund, Henrik, Jackstell, Ralf, Beller, Matthias

Hydrogenation of olefins is achieved using biowaste-derived cobalt chitosan catalysts. Characterization of the optimal Co@Chitosan-700 by STEM (scanning transmission electron microscopy), EELS (electron energy loss spectroscopy), PXRD (powder x-ray diffraction), and elemental analysis revealed the formation of a distinctive magnetic composite material with high metallic Co content. The general performance of this catalyst is demonstrated in the hydrogenation of 50 olefins including terminal, internal, and functionalized derivatives, as well as renew-ables. Using this nonnoble metal composite, hydrogenation of terminal C==C double bonds occurs under very mild and benign conditions (water or methanol, 40° to 60°C). The utility of Co@Chitosan-700 is showcased for efficient hydrogenation of the industrially relevant examples diisobutene, fatty acids, and their triglycerides. Because of the magnetic behavior of this material and water as solvent, product separation and recycling of the catalyst are straightforward.