材料科学
转化(遗传学)
金属
化学工程
锰
化学物理
过渡金属
无机化学
结晶学
亚稳态
作者
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
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-04-03
卷期号:20 (14): 11344-11357
标识
DOI:10.1021/acsnano.6c00961
摘要
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.
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