Facet-Dependent Adsorption of Pb(II) on Hematite (001), (116), and (104) Surfaces
Ping Chen, Micah P. Prange, Duo Song, Sungsik Lee, Sang Soo Lee, Juejing Liu, Yatong Zhao, Xiang Wang, Mark Engelhard, Yadong Zhou, Yanqiu Feng, Nikita Basilyan, Xiaoxu Li, Carolyn I. Pearce, Zhe-Ming Wang, Zihua Zhu, Kevin M. Rosso, Xin Zhang
Abstract
Hematite’s common (001) and (012) facets are frequently used in model studies of lead (Pb) adsorption behavior, but there is a lack of research on the high-energy facets, e.g., (104), present in nature. Also, few studies have attempted to connect the molecular details of facet-specific Pb adsorption to the macroscopic uptake behavior. To address these knowledge gaps, we investigated Pb(II) adsorption behaviors on facet-engineered hematite nanoparticles dominated by (001), (104), and (116). Adsorption experiments revealed significant variations in Pb(II) uptake among the three samples, with (001) demonstrating the highest capacity and (116) showing the best adsorption efficiency when normalized to the specific surface area. Adsorption kinetics followed the pseudo-second-order model, indicating that the adsorption process is governed mostly by chemisorption. Adsorption isotherms were well fitted by the Langmuir model, indicating that uptake proceeds until roughly monolayer adsorption. Detailed characterization revealed Pb(II) was adsorbed as single atoms with complex inner-sphere binding modes that varied across different facets, indicating that adsorption is both structurally and energetically facet-dependent. Coadsorption experiments further demonstrated Cu 2+, Zn 2+, and humic acid significantly promoted Pb(II) adsorption. This study advances the understanding of hematite surface reactivity in controlling macroscopic wet adsorption behaviors, providing valuable insights into the environmental fate of Pb(II).