Herein we present two new ferrocene compounds Fc3 and Fc4 with, respectively, propyl and butyl zwitterionic side chains. These compounds are highly soluble in water (0.66 M for Fc3 and 2.01 M for Fc4). When paired with anthraquinone-2,7-disulfonate as the anolyte, these zwitterionic ferrocenes exhibit excellent performance under neutral aqueous conditions. Voltage and energy efficiencies were ca. 88%, and the Coulombic efficiency was over 99% for both high-concentration redox flow batteries. We observed a difference in stability between the lengths of the zwitterionic chains, with Fc4 showing higher stability than Fc3, and the capacity decreased by ∼5% at the end of 20 cycles (∼1% per day). Density functional theory calculations revealed striking differences in the conformational properties between Fc3 and Fc4, with Fc4 retaining a linear structure of the side chain in solution, while Fc3 favored both linear and curved geometries.