Materials Research Express (Jan 2024)

Tin-antimony/carbon composite porous fibers: electrospinning synthesis and application in sodium-ion batteries

  • Xiong Chen,
  • Yusen Huang,
  • Maobin Zhang,
  • Yunlong Yu,
  • Xiaoyan Li,
  • Dagui Chen,
  • Jinquan Hong,
  • Shaowu Du,
  • Xiangfeng Guan

DOI
https://doi.org/10.1088/2053-1591/ad2c3d
Journal volume & issue
Vol. 11, no. 3
p. 035501

Abstract

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In this work, tin-antimony/carbon composites porous fibers were successfully synthesized by an electrospinning method combined with two-step heat treatment processes, in which SnCl _2 and SbCl _3 were used as tin and antimony sources, and polyacrylonitrile (PAN) and polymethyl methacrylate (PMMA) were used as binders and pore-forming agents. The as-synthesized tin-antimony/carbon composites were systematically characterized by x-ray Diffraction (XRD), Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Energy-Dispersive Spectrometer (EDS), x-ray Photoelectron Spectroscopy (XPS), and Thermogravimetric Analysis-Differential Scanning Calorimetry (TG-DSC). The results indicate that the composite material consists of one-dimensional nitrogen-doped carbon porous fibers as the main matrix, with a three-dimensional network structure in which Sn, SnO _2 , and SnSb particles are encapsulated. Furthermore, the tin-antimony/carbon composites porous fibers were utilized as self-supported negative electrode for sodium-ion batteries. The results showed that the SNbM-2 sample electrode calcined at 800 °C demonstrated the best cycling stability and rate capability among all the sample electrodes, with a discharge capacity of 319.5 mAh·g ^−1 maintained after 100 cycles at a current density of 0.1 A·g ^−1 . The excellent electrochemical performance of the SNbM-2 sample electrode is benefited from its unique porous structure and the carbon fiber network structure encapsulating Sn, SnO _2 , and SnSb particles, which could effectively shorten the Na ^+ ion transport distance and mitigate electrode volume expansion.

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