“…[23][24][25] In addition, although some inorganic supports such as active carbon materials possessed rich functional groups on the surface and their nature could be easily manipulated at a proper temperature for optimizing the interaction with the loaded metal, controlling the size distribution of particles was still difficult 27,28 due to the uneven dispersing density of the functional groups on the surface, especially when metal loadings were altered to a relative higher amount. 29,30 In contrast, in our study, the introduction of a capturing group (VTC) in a proper amount to copolymerize on the surface of polystyrene (with the molar ratio of VTC : styrene at 0.05) was veried to be a feasible way to optimize the electrostatic state of polystyrene substrate, which consequently facilitated the uniform anchoring of Pd precursors and the following in situ reduction to narrow-size-range distributed Pd nanoparticles (ca. 3.0-5.0 nm) in a broad loading range (from 0.2 wt% to 4.6 wt%) under protector-free conditions.…”