Journal
NEW JOURNAL OF CHEMISTRY
Volume 43, Issue 19, Pages 7386-7392Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9nj00884e
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Funding
- National Natural Science Foundation of China [51772334, 51778627, 51822812]
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Herein, the MoP@C nanocomposite was successfully fabricated via a facile sol-gel approach followed by an annealing process, which demonstrated excellent electrochemical properties as a novel anode for sodium storage. The addition of the surfactant Tween 80 led to the formation of strong P-C bonds, ensuring in situ formation of a thin carbon layer on the nanosized MoP particles, which could mitigate particle aggregation and maintain the stable framework. Moreover, owing to the synergistic effect between the MoP nanoparticles and the highly conductive carbon network, the MoP@C nanocomposite delivered high reversible capacity and a superior cyclability (maintaining 180.3 mA h g(-1) after 250 cycles at 500 mA g(-1)). In addition, the sodium-storage mechanism of MoP was unraveled by the combined analyses of in situ X-ray diffraction and ex situ transmission electron microscopy, confirming an incomplete conversion reaction during the sodiation/desodiation process; this provided an insight into the structural evolution and Na+-ion storage performance of phosphide anodes.
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