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Unveiling the Nature of Ultrastable Potassium Storage in Bi0.48Sb1.52Se3 Composite
Tong Yuan1, Jitong Yan2, Qingfeng Zhang1
1Key Laboratory of Low Dimensional Materials and Application Technology of Ministry of Education, School of Materials Science and Engineering, Xiangtan University, Xiangtan, Hunan 411105, People's Republic of China.
Abstract:
The conversion and alloying-type anodes for potassium-ion batteries (PIBs) have drawn attention. However, it is still a challenge to relieve the huge volume expansion/electrode pulverization. Herein, we synthesized a composite material comprising Bi0.48Sb1.52Se3 nanoparticles uniformly dispersed in carbon nanofibers (Bi0.48Sb1.52Se3@C). Benefiting from the synergistic effects of the high electronic conductivity of Bi0.48Sb1.52Se3 and the mechanical confinement of the carbon fiber that buffers the large chemomechanical stress, the Bi0.48Sb1.52Se3@C//K half cells deliver a high reversible capacity (491.4 mAh g-1, 100 cycles at 100 mA g-1) and an extraordinary cyclability (80% capacity retention, 1000 cycles at 1000 mA g-1). Furthermore, the Bi0.48Sb1.52Se3@C-based PIB full cells achieve a high energy density of 230 Wh kg-1. In situ transmission electron microscopy (TEM) reveals an intercalation, conversion, and alloying three-step reaction mechanism and a reversible amorphous transient phase. More impressively, the nanofiber electrode can almost return to its original diameter after the potassiation and depotassiation reaction, indicating a highly reversible volume change process, which is distinct from the other conversion type electrodes. This work reveals the stable potassium storage mechanisms of Bi0.48Sb1.52Se3@C composite material, which provides an effective strategy to enable conversion/alloying-type anodes for high performance PIBs for energy storage applications.
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