Xinran Liang, Xi Gao, Haoran Hu, Muammar Mansor, Fayang Guo, Bruno Lanson, Lei Wang, Fangdong Zhan, Yanqun Zu, Haesung Jung, Hui Li, Wenfeng Tan, Xionghan Feng, Biao Wan, James J. De Yoreo
Crystallization of poorly crystalline minerals generally remobilizes the adsorbed heavy metals. In contrast, we find that the conversion of poorly crystalline layered δ-MnO 2 to crystalline 2 × 2 tunneled α-MnO 2 significantly increases both the amount and stability of Pb 2+ immobilization. The varied characterization analyses reveal that Pb 2+ first exchanges surface K + associated with δ-MnO 2 and is then sequestered into α-MnO 2 2 × 2 tunnels via oriented attachment along the (001) plane. Without the crystallization process, Pb 2+ cannot substitute for tunnel K + in α-MnO 2 and can only weakly bind to the external (310) surface. Stability comparisons across outer-surface adsorption, wall substitution, and tunnel incorporation indicate that only tunnel-resident metals achieve strongly enhanced and persistent Pb sequestration. This study not only challenges the conventional understanding that mineral crystallization and layer-to-tunnel transformation lead to the release of adsorbed heavy metals but also suggests a potential strategy for selective metal trapping in engineered remediation materials and environmental matrices.