Zhang Siqi, Zhu Youliang, Wang Denghu, Li Chunguang, Han Yu, Shi Zhan, Feng Shouhua
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun, 130012, P. R. China.
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
Adv Sci (Weinh). 2022 May;9(14):e2200397. doi: 10.1002/advs.202200397. Epub 2022 Mar 20.
Calcium-ion batteries (CIBs) are considered as promising alternatives in large-scale energy storage due to their divalent electron redox properties, low cost, and high volumetric/gravimetric capacity. However, the high charge density of Ca contributes to strong electrostatic interaction between divalent Ca and hosting lattice, leading to sluggish kinetics and poor rate performance. Here, in situ formed poly(anthraquinonyl sulfide) (PAQS)@CNT composite is reported as nonaqueous calcium-ion battery cathode. The enolization redox chemistry of organics has fast redox kinetics, and the introduction of carbon nanotube (CNT) accelerates electron transportation, which contributes to fast ionic diffusion. As the conductivity of the PAQS is enhanced by the increasing content of CNT, the voltage gap is significantly reduced. The PAQS@CNT electrode exhibits specific capacity (116 mAh g at 0.05 A g ), high rate capacity (60 mAh g at 4 A g ), and an initial capacity of 82 mAh g at 1 A g (83% capacity retention after 500 cycles). The electrochemical mechanism is proved to be that the PAQS undergoes reduction reaction of their carbonyl bond during discharge and becomes coordinated by Ca and Ca(TFSI) species. Computational simulation also suggests that the construction of Ca and Ca(TFSI) co-intercalation in the PAQS is the most reasonable pathway.
钙离子电池(CIBs)因其二价电子氧化还原特性、低成本以及高体积/重量容量,被视为大规模储能领域有前景的替代方案。然而,钙的高电荷密度导致二价钙离子与主体晶格之间存在强烈的静电相互作用,致使动力学迟缓且倍率性能不佳。在此,原位形成的聚(蒽醌基硫醚)(PAQS)@碳纳米管(CNT)复合材料被报道可作为非水钙离子电池的正极。有机物的烯醇化氧化还原化学具有快速的氧化还原动力学,而碳纳米管(CNT)的引入加速了电子传输,这有助于快速的离子扩散。随着CNT含量增加提高了PAQS的导电性,电压间隙显著减小。PAQS@CNT电极展现出比容量(在0.05 A g 时为116 mAh g)、高倍率容量(在4 A g 时为60 mAh g)以及在1 A g 时的初始容量为82 mAh g(500次循环后容量保持率为83%)。电化学机理被证明是PAQS在放电过程中其羰基键发生还原反应,并与Ca和Ca(TFSI)物种配位。计算模拟还表明,在PAQS中构建Ca和Ca(TFSI)共嵌入是最合理的途径。