Sun Chaoyang, Ji Shan, Ma Xianguo, Wang Hui, Wang Xuyun, Linkov Vladimir, Wang Rongfang
State Key Laboratory Base for Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing 314001, China.
J Colloid Interface Sci. 2022 Oct;623:306-317. doi: 10.1016/j.jcis.2022.05.053. Epub 2022 May 13.
Porous carbon-supported transition metals and their compounds have attracted much attention as sulfur host materials for cathodes of lithium-sulfur batteries, due to their high chemisorption capacity and ability to catalyze the conversion of polysulfides. However, actual activity of these materials is not very high because of low specific surface areas of transition metal compounds synthesized at high temperatures. In this study, ultra-fine vanadium nitride particles with an average particle size of ca. 4 nm (VN/M/NC) are successfully grown on the surface of nitrogen-doped three-dimensional carbon using sp nitrogen atoms, resulting from melamine pyrolysis in the presence of ammonium metavanadate, as anchor points to lock vanadium atoms in the VN/M/NC material. When used as a cathode for lithium-sulfur battery, VN/M/NC demonstrates initial discharge specific capacity of 1080 mAh g at 0.2 C, and retains a discharge capacity of 475 mAh g at a high rate of 2 C. With capacity attenuation of only 0.037% per cycle after 500 cycles at 1 C, the newly obtained VN/M/NC can be a promising cathode material for lithium-sulfur batteries.
多孔碳负载的过渡金属及其化合物作为锂硫电池阴极的硫主体材料受到了广泛关注,这是由于它们具有高化学吸附能力以及催化多硫化物转化的能力。然而,由于在高温下合成的过渡金属化合物比表面积较低,这些材料的实际活性不是很高。在本研究中,平均粒径约为4纳米的超细氮化钒颗粒(VN/M/NC)成功地生长在氮掺杂三维碳的表面,利用偏钒酸铵存在下三聚氰胺热解产生的氮原子作为锚点,将钒原子锁定在VN/M/NC材料中。当用作锂硫电池的阴极时,VN/M/NC在0.2C下的初始放电比容量为1080 mAh g,在2C的高倍率下仍保持475 mAh g的放电容量。在1C下循环500次后,容量衰减仅为每循环0.037%,新获得的VN/M/NC有望成为锂硫电池的阴极材料。