No abstract

The Front Cover shows the generation of tailor‐made pores by the electrochemical activation of expanded graphite for a magnesium−organocation hybrid battery. Under the electric field, the organocations expand the graphene layers like drilling vehicles that open the undersea tunnel with sufficient space for the following submarines, which symbolizes the same organocations that freely move to store and release electricity efficiently through the tailor‐made pores that were generated by electrochemical activation. More information can be found in the Research Article type by S. K. Mohanty et al.

Persisting limitations of lithium‐ion batteries (LIBs) in terms of safety, energy and power density, natural resources, and the price call for expeditious research to develop the “beyond Li‐ion” technologies. In this regard, magnesium–organocation hybrid batteries (MOHB) hold the potential to address the above issues associated with LIBs by utilizing abundant and inexpensive elements of magnesium and carbon for the anode and cathode, respectively. Moreover, magnesium metal anode is highly energy‐dense yet less susceptible to the dendrite formation, enabling safer operation compared to lithium metal anodes. In this study, we targeted to increase the capacity and rate capability of porous carbon cathode of MOHB by generating tailor‐made pores, which were provided by the interlayer accommodation of solvated organic cations with controlled sizes during the electrochemical activation of expanded graphite. Our electrochemically activated expanded graphite can be used as an efficient cathode in MOHB with enhanced kinetics, specific capacitance, and cycle life.

Invited for this month′s cover are the groups of Prof. Hyun Deog Yoo and Prof. Jin Kyoon Park at Pusan National University, and Prof. Ji Heon Ryu at Tech University of Korea (Republic of Korea). The cover image illustrates the generation of tailor‐made pores by the electrochemical activation of expanded graphite for a magnesium–organocation hybrid battery. The Research Article itself is available at 10.1002/cssc.202300035.