Gao Ning, Li Bao, Zhang Yujiao, Li Wenbiao, Li Xue, Zhao Jie, Yue Wence, Xing Zhenyu, Wang Bao
State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
Nanjing IPE Institute of Green Manufacturing Industry, Nanjing 211135, China.
ACS Appl Mater Interfaces. 2021 Dec 8;13(48):57193-57203. doi: 10.1021/acsami.1c17374. Epub 2021 Nov 19.
Good electrical conductivity, strong catalytic activity, high interaction with lithium polysulfides (LIPSs), simple method, and low cost should be considered for the design and preparation of high-performance electrochemical catalysts that catalyze the conversion of LIPSs. In this work, we designed a bimetallic alloyed multifunctional interlayer with multiple adsorption/catalysis sites. The interwoven carbon fibers derived from bacterial cellulose (BC) not only contribute to reducing metal ions to metals but also confine the growth of Co-Fe alloys formed in situ. The metal supported on carbon is very effective for the conversion of LIPSs due to its high adsorption and catalytic sites. In addition, the synergistic effect between Fe and Co species leads to excellent bifunctional catalytic activity. Through detailed electrochemical analysis and theoretical calculations, we revealed that CoFe@CNFs has superior electrocatalytic activity, and the lithium-sulfur (Li-S) batteries with a catalytic interlayer can deliver satisfactory rate and cycle performance. At a high current density of 2C, the discharge capacity can still reach 627 mAh g. At a current density of 1C, the Coulombic efficiency is maintained at a level close to 100% during the whole cycle process and a satisfying low capacity decay of 0.08% per cycle. More importantly, even if the ambient temperature drops to 0 °C, the Li-S battery using the interlayer can still be charged and discharged normally and shows acceptable discharge capacity, which shows that it has good rate kinetics.
在设计和制备催化多硫化锂(LIPSs)转化的高性能电化学催化剂时,应考虑良好的导电性、强催化活性、与多硫化锂的高相互作用、制备方法简单以及成本低等因素。在这项工作中,我们设计了一种具有多个吸附/催化位点的双金属合金多功能中间层。源自细菌纤维素(BC)的交织碳纤维不仅有助于将金属离子还原为金属,还限制了原位形成的Co-Fe合金的生长。负载在碳上的金属由于其高吸附和催化位点,对LIPSs的转化非常有效。此外,Fe和Co物种之间的协同效应导致了优异的双功能催化活性。通过详细的电化学分析和理论计算,我们发现CoFe@CNFs具有优异的电催化活性,带有催化中间层的锂硫(Li-S)电池能够提供令人满意的倍率和循环性能。在2C的高电流密度下,放电容量仍可达到627 mAh g。在1C的电流密度下,整个循环过程中的库仑效率保持在接近100%的水平,且每循环的容量衰减低至0.08%,令人满意。更重要的是,即使环境温度降至0°C,使用该中间层的Li-S电池仍能正常充放电,并显示出可接受的放电容量,这表明它具有良好的倍率动力学。