Recently, the focus of proton-exchange membrane fuel cell (PEMFC) applications has shifted from fuel cell vehicles (FCVs) to heavy-duty vehicles (HDVs), necessitating enhanced fuel cell durability. The degradation of carbon-supported metal nanoparticle catalysts and electrolyte membranes are the primary factors responsible for fuel cell durability. Particularly in the context of HDVs, augmenting the chemical stability of electrolyte membranes, such as Nafion, stands as a crucial factor in improving fuel cell lifetime. The degradation mechanism of Nafion is believed to involve the cleavage of polymer chains by OH∙ radicals, formed by crossover hydrogen and crossover oxygen in the presence of trace transition metal ions. A common strategy to mitigate Nafion's chemical degradation involves adding radical quenchers like cerium ion (Ce+) to Nafion. However, Ce+ may migrate out of Nafion during fuel cell operation, leading to a decline in its highly efficient radical quenching ability over extended operational periods.In this study, we demonstrate that a fullerene-derived radical quencher with multiple hydroxy groups significantly contributes to enhancing the durability of Nafion. Our approach involves synthesizing fullerene derivatives with various kind of hydroxy and functional groups for remarkable water solubility to realize their homogeneous dispersion within the Nafion membrane. The abundant functional groups also aid in improving proton conductivity. Moreover, the chelating effect of the spherically distributed functional groups immobilizes themselves, preventing any observed leakage from the Nafion membrane. These fullerene-derivative radical quenchers effectively enhance fuel cell durability and hold promise for future applications in HDVs.This study was supported by the New Energy and Industrial Technology Development Organization (NEDO), Japan (JPNP20003).