4.8 Article

In-Situ Growing Mesoporous CuO/O-Doped g-C3N4 Nanospheres for Highly Enhanced Lithium Storage

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 11, 期 36, 页码 32957-32968

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b10171

关键词

CuO; g-C3N4; in situ growth; lithium-ion batteries; reaction kinetics

资金

  1. National Key R&D Program of China [2016YFA0202602]
  2. Academy of Scientific Research & Technology (ASRT, Egypt)
  3. National Natural Science Foundation of China [U1663225, 21671155, 21805220]
  4. Natural Science Foundation of Hubei Province [2018CFB242, 2018CFA054]
  5. Major Technology Innovation of Hubei Province [2018AAA012]
  6. Program for Changjiang Scholars Innovative Research Team in University [IRT_15R52]
  7. Science & Technology Development Fund (STDF, Egypt)

向作者/读者索取更多资源

The development of lithium-ion batteries using transition metal oxides has recently become more attractive, due to their higher specific capacities, better rate capability, and high energy densities. Herein, the in situ growth of advanced mesoporous CuO/O-doped g-C3N4 nanospheres is carried out in a two step hydrothermal process at 180 degrees C and annealing in air at 300 degrees C. When used as an anode material, the CuO/O-doped g-C3N4 nanospheres achieve a high reversible discharge specific capacity of 738 mAhg-1 and a capacity retention of similar to 75.3% after 100 cycles at a current density 100 mAg(-1) compared with the pure CuO (412 mAhg(-1), 47%) and O-doped g-C3N4 (66 mAhg(-1), 53%). Even at high current density 1 Ag-1, they exhibit a reversible discharge specific capacity of 503 mAhg(-1) and capacity retention similar to 80% over 500 cycles. The excellent electrochemical performance of the CuO/O-doped g-C3N4 nanocomposite is attributed to the following factors: (I) the in situ growing CuO/O-doped g-C3N4 avoids CuO nanoparticle aggregation, leading to the improved lithium ion transfer and electrolyte penetration inside the CuO/O-doped g-C3N4 anode, thus promoting the utilization of CuO; (II) the porous structure provides efficient space for Li+ transfer during the insertion/extraction process to avoid large volume changes; (III) the O-doping g-C3N4 decreases its band gap, ensuring the increased electrical conductivity of CuO/O-doped g-C3N4; and (IV) the strong interaction between CuO and O-doped g-C3N4 ensures the stability of the structure during cycling.

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