Enabling Selenium‐Rich SexSy Cathodes to Work in Carbonate‐Based Electrolytes

Abstract Lithium–sulfur/selenium batteries have attracted broad interest and achieved good performance using ether‐based electrolytes. However, when the ether‐based electrolytes are employed, Li–S/Se battery systems still have several inevitable drawbacks inhibiting their practical applications, such as intermediate product dissolution issues, and a dependency on a high content of electrolyte. Thus, it is urgent to pay attention to the electrochemical properties of Se x S y cathodes in carbonate‐based electrolytes, which may avoid the above mentioned problems. In this work, a series of mesoporous carbon/Se x S y (CMK‐3/Se x S y ) composites with covalent Se‐S bonds and different Se/S molar ratios are prepared and their working mechanism in carbonate‐based electrolytes is systematically investigated by combining experimental analysis and theoretical calculations. This work finds that the Se in the CMK‐3/Se x S y cathode is beneficial for the transportation of Li + ions and forms a thin cathode electrolyte interphase (CEI) during the discharge–charge process. Furthermore, S substitution in Se 8 molecules can enhance the specific capacity and lower the bond breaking and lithiation energies. The optimal CMK‐3/Se x S y cathode delivers outstanding performance with a high reversible capacity of 609 mA h g −1 at 1 A g −1 over 300 cycles.