Three‐dimensional Honeycomb MoP@C Nanocomposite with Advanced Sodium/Potassium Ion Storage Performance

Author:

Wang Rui1,Xu Bangqiang1,Zheng Cheng2,Deng Yue1,Fan Kai1,Wang Nana3,Hu Kunkun1,Zhang Qiang1,Zou Guifu1,Zhai Yanjun4,Bai Zhongchao1ORCID,Xu Xun3

Affiliation:

1. College of Mechanical and Electronic Engineering Shandong University of Science and Technology Qingdao 266590 Shandong PR China

2. Key Laboratory of Colloid and Interface Chemistry Ministry of Education School of Chemistry and Chemical Engineering Shandong University Jinan China

3. Univ Wollongong Australian Inst Innovat Mat, Inst Superconducting & Elect Mat, Innovat Campus North Wollongong, NSW 2500 Australia

4. Shandong Provincial Key Laboratory/Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology Liaocheng University Liaocheng 252059 China

Abstract

AbstractMoP@C nanocomposite, combined three‐dimensional (3D) honeycomb carbon matrix with molybdenum phosphide, was synthesized through a simple hard template method followed by high‐temperature phosphating treatment. The MoP@C has shown excellent sodium and potassium‐ion storage properties applied as anode materials for sodium‐ion batteries (SIBs) and potassium‐ion batteries (PIBs). The MoP@C composite maintains a high reversible specific capacity of 250 mAh g−1 in SIBs after 100 cycles at 0.5 A g−1. Furthermore, even at a high current density of 5 A g−1, it still delivers a specific capacity of 200.5 mAh g−1. Additionally, the nanocomposite holds 147.2 mAh g−1 at a high current density of 1 A g−1 in PIBs. The excellent electrochemical performance benefits from the synergistic effect of the hierarchical MoP@C nanostructure. The exquisite porous nano‐frame with higher conductivity and larger specific surface area, the active substance is fully infiltrated in the electrolyte, and successfully shortens the diffusion distance of electrons and ions. Moreover, the cavity in the heterostructure effectively inhibits the instinctive aggregation of MoP and simultaneously alleviates the volume expansion during the intercalation and deintercalation of ions in the charge and discharge process, enabling the excellent rate performance and long cycle life of the MoP@C electrode. The designed MoP@C composite shows excellent electrochemical cycle performance and rate performance as anode materials for sodium/potassium‐ion batteries. The MoP@C composite maintained a high reversible specific capacity of 250 mAh g−1 in sodium‐ion batteries after 100 cycles at the current density of 0.5 A g−1. Furthermore, even at a high current density of 5 A g−1, it still delivered a specific capacity of 200.5 mAh g−1. Moreover, MoP@C composite materials also show excellent performance as anode material of potassium‐ion batteries, with a specific capacity of 147.2 mAh g−1 at the high current density of 1 A g−1. In summary, the excellent electrochemical performance of MoP@C composite materials fully proves that they can greatly improve the stability of the structure and reversibility as electrode materials, and lays a foundation for the further application of electrochemical energy storage devices in large‐scale applications.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

Wiley

Subject

General Chemistry

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