Rechargeable Mg battery has been considered a major candidate as a beyond lithium ion battery technology, which is apparent through the tremendous works done in the field over the past decades. The challenges for realization of Mg battery are complicated, multidisciplinary, and the tremendous work done to overcome these challenges is very hard to organize in a regular review paper. Additionally, we claim that organization of the huge amount of information accumulated by the great scientific progress achieved by various groups in the field will shed the light on the unexplored research domains and give clear perspectives and guidelines for next breakthrough to take place. In this Perspective, we provide a convenient map of Mg battery research in a form of radar chart of Mg electrolytes, which evaluates the electrolyte under the important components of Mg batteries. The presented radar charts visualize the accumulated knowledge on Mg battery and allow for navigation of not only the current research state but also future perspective of Mg battery at a glance.
A series of copper-doped zinc oxide films were grown by pulsed-laser ablation. Films grown under conditions that produced n-type ZnO were nonmagnetic while those grown under conditions that produced p-type were ferromagnetic with a Curie temperature above 350 K. The magnetic moment per copper atom decreased as the copper concentration increased. An explanation for this result is proposed based on the distance between nearest-neighbor copper atoms.
Magnesium batteries have been considered to be one of the promising beyond lithium ion technologies due to magnesium's abundance, safety, and high volumetric capacity. However, very few materials show reversible performance as a cathode in magnesium ion systems. We present herein the best reported cycling performances of MnO2 as a magnesium battery cathode material. We show that the previously reported poor Mg(2+) insertion/deinsertion capacities in MnO2 can be greatly improved by synthesizing self-standing nanowires and introducing a small amount of water molecules into the electrolyte. Electrochemical and elemental analysis results revealed that the magnitude of Mg(2+) insertion into MnO2 highly depends on the ratio between water molecules and Mg(2+) ions present in the electrolyte and the highest Mg(2+) insertion capacity was observed at a ratio of 6H2O/Mg(2+) in the electrolyte. We demonstrate for the first time, that MnO2 nanowire electrode can be "activated" for Mg(2+) insertion/deinsertion by cycling in water containing electrolyte resulting in enhanced reversible Mg(2+) insertion/deinsertion even with the absence of water molecules. The MnO2 nanowire electrode cycled in dry Mg electrolyte after activation in water-containing electrolyte showed an initial capacity of 120 mA h g(-1) at a rate of 0.4 C and maintained 72% of its initial capacity after 100 cycles.
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