Affiliation:
1. Key Laboratory of Superlight Materials and Surface Technology (Ministry of Education) College Material Science and Chemical Engineering Harbin Engineering University Harbin 150001 P. R. China
2. Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) College of Chemistry Nankai University Tianjin 300071 China
Abstract
AbstractMoS2, as a classical 2D material, becomes a capable anode candidate for sodium‐ion batteries. However, MoS2 presents a disparate electrochemical performance in the ether‐based and ester‐based electrolyte with unclear mechanism. Herein, tiny MoS2 nanosheets embedded in nitrogen/sulfur‐codoped carbon (MoS2@NSC) networks are designed and fabricated through an uncomplicated solvothermal method. Thanks to the ether‐based electrolyte, the MoS2@NSC shows a unique capacity growth in the original stage of cycling. But in the ester‐based electrolyte, MoS2@NSC shows a usual capacity decay. The increasing capacity puts down to the gradual transformation from MoS2 to MoS3 with the structure reconstruction. Based on the above mechanism, MoS2@NSC demonstrates an excellent recyclability and the specific capacity keeps around 286 mAh g−1 at 5 A g−1 after 5000 cycles with an ultralow capacity fading rate of only 0.0034% per cycle. In addition, a MoS2@NSC‖Na3V2(PO4)3 full cell with ether‐based electrolyte is assembled and demonstrates a capacity of 71 mAh g−1, suggesting the potential application of MoS2@NSC. Here the electrochemical conversion mechanism of MoS2 is revealed in the ether‐based electrolyte and significance of the electrolyte design on the promoting Na ion storage behavior is highlighted.
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
24 articles.
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