4.8 Article

Carbon-Encapsulated Fe3O4 Nanoparticles as a High-Rate Lithium Ion Battery Anode Material

Journal

ACS NANO
Volume 7, Issue 5, Pages 4459-4469

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn401059h

Keywords

high rate; core-shell; nanohybrid; carbon-encapsulated Fe3O4 nanoparticles; 2D nanosheet; in situ synthesis; energy storage

Funding

  1. National Natural Science Foundation of China [51002188, 51272173]
  2. National Excellent Doctoral Dissertation of China [201145]
  3. Program for New Century Excellent Talents in University [NCET-12-0408]
  4. Natural Science Foundation of Tianjin City [12JCYBJC11700]
  5. Elite Scholar Program of Tianjin University
  6. Innovation Foundation of Tianjin University
  7. National Basic Research Program of China [2010CB934700]
  8. Projects for the Science & Technology Pillar Program of Tianjin City [12ZCZDGX00800]

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A facile and scalable in situ synthesis strategy is developed to fabricate carbon-encapsulated Fe3O4 nanoparticles homogeneously embedded in two-dimensional (2D) porous graphitic carbon nanosheets (Fe3O4@C@PGC nanosheets) as a durable high-rate lithium ion battery anode material. With assistance of the surface of NaCl particles, 20 Fe@C@PGC nanosheets can be in situ synthesized by using the Fe(NO3)(3) center dot 9H(2)O and C6H12O6 as the metal and carbon precursor, respectively. After annealing under air, the Fe@C@PGC nanosheets can be converted to Fe3O4@C@PGC nanosheets, in which Fe3O4 nanoparticles (similar to 18.2 nm) coated with conformal and thin onion-like carbon shells are homogeneously embedded in 2D high-conducting carbon nanosheets with a thickness of less than 30 nm. In the constructed architecture, the thin carbon shells can avoid the direct exposure of encapsulated Fe3O4 to the electrolyte and preserve the structural and Interfacial stabilization of Fe3O4 nanoparticles. Meanwhile, the flexible and conductive PGC nanosheets can accommodate the mechanical stress induced by the volume change of embedded Fe3O4@C nanoparticles as well as inhibit the aggregation of Fe3O4 nanoparticles and thus maintain the structural and electrical integrity of the Fe3O4@C@PGC electrode during the lithiation/delithiation processes. As a result, this Fe3O4@C@PGC electrode exhibits superhigh rate capability (858, 587, and 311 mAh/g at 5, 10, and 20 C, respectively, 1 C = 1 A/g) and extremely excellent cyding performance at high rates (only 3.47% capacity loss after 350 cycles at a high rate of 10 C), which is the best one ever reported for an Fe3O4-based electrode including various nanostructured Fe3O4 anode materials, composite electrodes, etc.

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