Yu Wei-jie, Lu Yong-hong, Liu Shu-he, Zhou Lie-xing, Li Kong-zhai
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引用次数: 0
Abstract
Lithium-sulfur batteries have an ultra-high theoretical specific capacity of 1675 mAh g−1 and a specific energy density of 2600 Wh kg−1, but the low conductivity of sulfur and its discharge products, volume change of sulfur species during charge and discharge as well as the intrinsic lithium polysulfide shuttle characteristics hinder the full potential of the batteries. In this study, porous carbon micron fibers (PCMFs) were prepared by carbonization of cotton at 900 °C, and V5S8/PCMF composites were prepared by chemical vapor deposition of V5S8 nanoparticles on PCMFs. It is shown that the electrochemical performance of the battery with V5S8/PCMF cathode host is significantly improved compared with that of the battery using only PCMF host, thanks to the catalytic conversion of V5S8 towards sulfur species. Lithium-sulfur battery with V5S8/PCMF/S cathode has an initial discharge specific capacity of 1034 mAh g−1, a capacity of 762.9 mAh g−1 after 100 cycles and a capacity decay rate of 0.28% per cycle at 0.2 C, much improved than the battery with PCMF/S cathode; when cycling at 1 C for 400 cycles, the capacity decay rate is only 0.11% per cycle, showing superior cycle stability. With sulfur areal loading of 4.62 mg cm−2, there is still a first discharge capacity of 852.2 mAh g−1 at 0.2 C. This CVD method might offer a feasible route for preparing transition metal sulfide for improving the performance of lithium-sulfur batteries.
锂硫电池具有1675 mAh g−1的超高理论比容量和2600 Wh kg−1的比能量密度,但硫及其放电产物的低电导率、充放电过程中硫种的体积变化以及锂多硫化物固有的切换特性阻碍了电池的充分发挥潜力。本研究采用900℃炭化棉花制备多孔炭微米纤维(PCMFs),并在PCMFs上化学气相沉积V5S8纳米粒子,制备了V5S8/PCMF复合材料。结果表明,V5S8/PCMF阴极主体电池的电化学性能比仅使用PCMF主体电池的电化学性能有显著提高,这是由于V5S8对硫物质的催化转化。V5S8/PCMF/S阴极锂硫电池的初始放电比容量为1034 mAh g−1,循环100次后的放电比容量为762.9 mAh g−1,在0.2 C下,每循环的容量衰减率为0.28%,比PCMF/S阴极锂硫电池有很大提高;在1℃下循环400次时,每循环容量衰减率仅为0.11%,具有良好的循环稳定性。当硫的面积载荷为4.62 mg cm−2时,在0.2℃下仍有852.2 mAh g−1的首次放电容量。该方法为制备过渡金属硫化物以提高锂硫电池的性能提供了一条可行的途径。
期刊介绍:
The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry.
The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces.
The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis.
The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.