FSI − -based ionic liquids (ILs) are promising electrolyte candidates for longlife and safe lithium metal batteries (LMBs). However, their practical application is hindered by sluggish Li + transport at room temperature. Herein, it is shown that additions of bis(2,2,2-trifluoroethyl) ether (BTFE) to LiFSI-Pyr 14 FSI ILs can effectively mitigate this shortcoming, while maintaining ILs′ high compatibility with lithium metal. Raman spectroscopy and small-angle X-ray scattering indicate that the promoted Li + transport in the optimized electrolyte, [LiFSI] 3 [Pyr 14 FSI] 4 [BTFE] 4 (Li 3 Py 4 BT 4 ), originates from the reduced solution viscosity and increased formation of Li + -FSI − complexes, which are associated with the low viscosity and non-coordinating character of BTFE. As a result, Li/LiFePO 4 (LFP) cells using Li 3 Py 4 BT 4 electrolyte reach 150 mAh g −1 at 1 C rate (1 mA cm −2 ) and a capacity retention of 94.6% after 400 cycles, revealing better characteristics with respect to the cells employing the LiFSI-Pyr 14 FSI (operate only a few cycles) and commercial carbonate (80% retention after only 218 cycles) electrolytes. A wide operating temperature (from −10 to 40 °C) of the Li/Li 3 Py 4 BT 4 /LFP cells and a good compatibility of Li 3 Py 4 BT 4 with LiNi 0.5 Mn 0.3 Co 0.2 O 2 (NMC532) are demonstrated also. The insight into the enhanced Li + transport and solid electrolyte interphase characteristics suggests valuable information to develop IL-based electrolytes for LMBs.The ORCID identification number(s) for the author(s) of this article can be found under

For the growth of 2D transition metal dichalcogenides, such as molybdenum (MoS2) and tungsten disulfides (WS2), metalorganic chemical vapor deposition (MOCVD) routes are favorable due to their superior scalability, the possibility to tune the processing temperatures by a proper choice of reactants thus avoiding the need for a postdeposition treatment. Herein, the first example of a promising MOCVD route for the direct fabrication of MoS2 and WS2 layers under moderate process conditions is reported. This straightforward route is successfully realized by the combination of metalorganic precursors of Mo or W bearing the amidinato ligand with just elemental sulfur. The formation of stoichiometric hexagonal 2H‐MoS2 and 2H‐WS2 is demonstrated which is confirmed by Raman, X‐ray diffraction, and X‐ray photoelectron spectroscopy studies. The deposited layers are evaluated for their electrocatalytic activity in hydrogen evolution reaction as a proof of principle for application in water splitting devices.

The development of alternative anode materials with higher volumetric and gravimetric capacity allowing for fast delithiation and, even more important, lithiation is crucial for next‐generation lithium‐ion batteries. Herein, the development of a completely new active material is reported, which follows an insertion‐type lithiation mechanism, metal‐doped CeO2. Remarkably, the introduction of carefully selected dopants, herein exemplified for iron, results in an increase of the achievable capacity by more than 200%, originating from the reduction of the dopant to the metallic state and additional space for the lithium ion insertion due to a significant off‐centering of the dopant atoms in the crystal structure, away from the original Ce site. In addition to the outstanding performance of such materials in high‐power lithium‐ion full‐cells, the selective reduction of the iron dopant under preservation of the crystal structure of the host material is expected to open up a new field of research.

In this paper, a direct chemical vapor deposition (CVD) approach is applied for the first time to synthesize high quality copper oxide (CuO), copper tungstate (CuWO4) and tungsten oxide (WO3) on F:SnO2 (FTO) substrates for photocatalytic water splitting.