Chen Chih-Jung, Huang Chih-Sheng, Huang Yu-Cheng, Wang Fu-Ming, Wang Xing-Chun, Wu Ching-Chen, Chang Wen-Sheng, Dong Chung-Li, Yin Li-Chang, Liu Ru-Shi
Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan.
Department of Physics, Tamkang University, Tamsui 25137, Taiwan.
ACS Appl Mater Interfaces. 2021 Feb 10;13(5):6156-6167. doi: 10.1021/acsami.0c17942. Epub 2021 Jan 28.
Li-CO batteries have recently attracted attention as promising candidates for next-generation energy storage devices due to their extremely high theoretical energy density. The real application of Li-CO cells involves addressing several drawbacks, including high charging potential, poor coulombic efficiency, and low rechargeability. Molybdenum disulfide supported on carbon nanotubes (MoS/CNT) with various ratios functioned as a cathode catalyst for Li-CO batteries. The optimal MoS/CNT composite achieved a maximum discharge capacity of 8551 mAh g with a coulombic efficiency of 96.7%. This hybrid also obtained an initial charging plateau of 3.87 V at a current density of 100 mA g with a cutoff capacity of 500 mAh g. It provided ideal electrochemical stability of 142 cycles at the current densities of 100 mA g, which was comparable with that of some precious metal catalysts. This optimized MoS/CNT was also cycled at 200 and 400 mA g for 112 and 55 times, respectively. Density functional theory calculations demonstrated that the sulfided Mo-edge (s-Mo-edge) on MoS materials showed appropriate adsorption strengths of Li, CO, and LiCO. Moreover, joint results of Raman profiles and extended X-ray absorption fine structure spectra elucidated that the catalytic efficiencies of MoS/CNT hybrids were proportional to the quantities of exposed s-Mo-edge active sites.
锂-二氧化碳电池因其极高的理论能量密度,最近作为下一代储能设备的有前景候选者而受到关注。锂-二氧化碳电池的实际应用涉及解决几个缺点,包括高充电电位、低库仑效率和低可再充电性。负载在碳纳米管上的不同比例的二硫化钼(MoS₂/CNT)用作锂-二氧化碳电池的阴极催化剂。最佳的MoS₂/CNT复合材料实现了8551 mAh g的最大放电容量,库仑效率为96.7%。这种复合材料在100 mA g的电流密度下,截止容量为500 mAh g时,还获得了3.87 V的初始充电平台。它在100 mA g的电流密度下提供了142次循环的理想电化学稳定性,这与一些贵金属催化剂相当。这种优化的MoS₂/CNT在200 mA g和400 mA g下也分别循环了112次和55次。密度泛函理论计算表明,MoS₂材料上的硫化钼边缘(s-Mo-edge)对Li、CO和LiCO显示出适当的吸附强度。此外,拉曼光谱和扩展X射线吸收精细结构光谱的联合结果表明,MoS₂/CNT复合材料的催化效率与暴露的s-Mo-edge活性位点的数量成正比。