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Nanorod-like CuS and Cu2 S have been fabricated by a hydrothermal approach without using any surfactant and template. The electrochemical behavior of CuS and Cu2 S nanorod anodes for lithium-ion batteries reveal that they exhibit stable lithium-ion insertion/extraction reversibility and outstanding rate capability. Both of the electrodes exhibit excellent capacity retentions irrespective of the rate used, even at a high current density of 3200 mA g(-1) . More than 370 mAh g(-1) can be retained for the CuS electrode and 260 mAh g(-1) for the Cu2 S electrode at the high current rate. After 100 cycles at 100 mA g(-1) , the obtained CuS and Cu2 S electrodes show discharge capacities of 472 and 313 mAh g(-1) with retentions of 92% and 96%, respectively. Together with the simplicity of fabrication and good electrochemical properties, CuS and Cu2 S nanorods are promising anode materials for practical use the next-generation lithium-ion batteries.

Given the limitations inherent in current intercalation‐based Li‐ion batteries, much research attention has focused on potential successors to Li‐ion batteries such as lithium–sulfur (Li‐S) batteries and lithium–oxygen (Li‐O2) batteries. In order to realize the potential of these batteries, the use of metallic lithium as the anode is essential. However, there are severe safety hazards associated with the growth of Li dendrites, and the formation of “dead Li” during cycles leads to the inevitable loss of active Li, which in the end is undoubtedly detrimental to the actual energy density of Li‐metal batteries. For Li‐metal batteries under practical conditions, a low negative/positive ratio (N/P ratio), a electrolyte/cathode ratio (E/C ratio) along with a high‐voltage cathode is prerequisite. In this Review, we summarize the development of new electrolyte systems for Li‐metal batteries under practical conditions, revisit the design criteria of advanced electrolytes for practical Li‐metal batteries and provide perspectives on future development of electrolytes for practical Li‐metal batteries.

The lack of suitable high-voltage cathode materials has hindered the development of rechargeable magnesium batteries (RMBs). Here, mesoporous Na V (PO ) /C (NVP/C) spheres have been synthesized through a facile spray-drying-annealing method, and their electrochemically desodiated phase NaV (PO ) /C (ED-NVP/C) has been investigated as an intercalation host for Mg ions. The obtained ED-NVP/C exhibits an average discharge voltage of around 2.5 V (vs. Mg /Mg), higher than those of most previously reported cathode materials. In addition, it can deliver an initial discharge capacity of 88.8 mA h g at 20 mA g , with good cycling stability. Ex situ X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results demonstrate that the electrochemical reaction is based on an intercalation mechanism and shows good reversibility. Galvanostatic intermittent titration technique (GITT) data have revealed that the intercalation process involves a two-phase transition. The reported ED-NVP/C cathode material with high working voltage offers promising potential for application in RMBs.

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