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

材料科学 介孔材料 化学工程 兴奋剂 锂(药物) 纳米复合材料 电解质 退火(玻璃) 带隙 纳米技术 纳米颗粒 阳极 电化学 电极 复合材料 光电子学 催化作用 物理化学 工程类 内分泌学 生物化学 化学 医学
作者
Hemdan S. H. Mohamed,Liang Wu,Chaofan Li,Zhi‐Yi Hu,Yu Li,Zhao Deng,Lihua Chen,Yu Li,Bao‐Lian Su
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (36): 32957-32968 被引量:87
标识
DOI:10.1021/acsami.9b10171
摘要

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 °C and annealing in air at 300 °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 ∼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 ∼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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