Technical bottlenecks of polyselenide shuttling and material volume variation significantly hamper the development of emerging sodium–selenium (Na–Se) batteries. The nanopore structure of substrate materials is demonstrated to play a vital… Click to show full abstract
Technical bottlenecks of polyselenide shuttling and material volume variation significantly hamper the development of emerging sodium–selenium (Na–Se) batteries. The nanopore structure of substrate materials is demonstrated to play a vital role in stabilizing Se cathodes and approaching superior Na-ion storage properties. Herein, an ideal nanorod-like trimodal hierarchical porous carbon (THPC) host is fabricated through a facile one-step carbonization method for advanced Na–Se batteries. The THPC possesses a trimodal nanopore structure encompassing micropores, mesopores, and macropores, and functions as a good accommodator of Se molecules, a reservoir of polyselenide intermediates, a buffer for volume expansion of Se species during sodiation, and a promoter for electron/ion transfer in the electrochemical process. As a result, Na–Se batteries assembled with the Se–THPC composite cathode realize high utilization of Se, fast redox kinetics, and excellent cyclability. Furthermore, the Na-ion storage mechanism of the well-designed Se–THPC composite is profoundly revealed by in situ visual characterization techniques.
               
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