Liu Jing, Dong Dengpan, Caro Alan Larrea, Andreas Nicolai Sage, Li Zongjian, Qin Yunan, Bedrov Dimitry, Gao Tao
Department of Chemical Engineering and Department of Material Science and Engineering, University of Utah, Salt Lake City, Utah 84114, United States.
ACS Cent Sci. 2022 Jun 22;8(6):729-740. doi: 10.1021/acscentsci.2c00293. Epub 2022 May 12.
Iron (Fe) metal batteries, such as Fe-ion batteries and all Fe flow batteries, are promising energy storage technologies for grid applications due to the extremely low cost of Fe and Fe salts. Nonetheless, the cycle life of Fe metal batteries is poor primarily due to the low Coulombic efficiency of the Fe deposition/stripping reaction. Current aqueous electrolytes based on Fe chloride or sulfate salts can only operate at a Coulombic efficiency of <91% under mild operation conditions (<5 mA/cm), largely due to undesired hydrogen evolution reaction (HER). This work reports a series of novel Fe electrolytes, Fe electrolytes reinforced with Mg ions (FERMI) and Ca ions (FERCI), which have remarkably better Coulombic efficiency, higher conductivity, and faster deposition/stripping kinetics. By the addition of 4.5 M MgCl or CaCl into the baseline FeCl electrolyte, the Fe deposition/stripping efficiency can be significantly improved to 99.1%, which greatly boosts the cycling performance of Fe metal batteries in both half-cells and full-cells. Mechanistic studies reveal that the remarkably improved efficiency is due to a reduced amount of "dead Fe" as well as suppressed HER. By the combination of experiments and molecular dynamics and density functional theory computation, the electrolyte structure is revealed, and the mechanism for enhanced water reduction resistance is elucidated. These novel electrolytes not only enable a highly reversible Fe metal anode for low-cost energy storage technologies but also have the potential to address the HER side reaction problem in other electrochemical technologies based on aqueous electrolytes, such as CO reduction, NH synthesis, etc.
铁(Fe)金属电池,如铁离子电池和全铁液流电池,由于铁和铁盐的成本极低,是用于电网应用的很有前景的储能技术。尽管如此,铁金属电池的循环寿命较差,主要原因是铁沉积/剥离反应的库仑效率较低。目前基于氯化铁或硫酸铁盐的水性电解质在温和操作条件下(<5 mA/cm²)只能在库仑效率<91%的情况下运行,这主要是由于不希望发生的析氢反应(HER)。这项工作报道了一系列新型铁电解质,即添加镁离子增强的铁电解质(FERMI)和添加钙离子增强的铁电解质(FERCI),它们具有显著更好的库仑效率、更高的电导率和更快的沉积/剥离动力学。通过向基线氯化铁电解质中添加4.5 M氯化镁或氯化钙,铁沉积/剥离效率可显著提高到99.1%,这极大地提升了铁金属电池在半电池和全电池中的循环性能。机理研究表明,效率的显著提高是由于“死铁”量的减少以及析氢反应的抑制。通过实验与分子动力学以及密度泛函理论计算相结合,揭示了电解质结构,并阐明了增强抗析氢能力的机理。这些新型电解质不仅为低成本储能技术提供了高度可逆的铁金属阳极,而且有可能解决其他基于水性电解质的电化学技术中的析氢副反应问题,如一氧化碳还原、氨合成等。