Theoretical Study of Small Iron-Oxyhydroxide Clusters and Formation of Ferrihydrite

被引:32
作者
Das, Bidisa [1 ]
机构
[1] Indian Assoc Cultivat Sci, Tech Res Ctr, 2A & 2B Raja SC Mullick Rd, Kolkata 700032, India
关键词
MOLECULAR-DYNAMICS SIMULATION; DENSITY-FUNCTIONAL THEORY; ENERGY; HYDROLYSIS; HETEROPOLY; 1ST-PRINCIPLES; APPROXIMATION; EXCHANGE; ION;
D O I
10.1021/acs.jpca.7b09470
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrolysis of iron compounds in water leads to the formation of Fe(III) oyxhydroxide-based minerals like ferrihydrite, which act as natural scavengers of inorganic contaminants in the environment. Though studied widely, experimental identification of these oxyhydroxides remains very difficult due to their extreme reactivity. The present study theoretically investigates the formation of Fe(III) oxyhydroxides starting from a single hydrated Fe(III) ion, modeling the formation of larger clusters gradually. The structures, formation enthalpies, and free energies of dimers, trimers, tetramers, and even larger Fe(III) oxyhydroxide clusters comprising of Fe-5, Fe-7, and Fe-13-Keggin ions in gaseous phase and in aqueous medium (using self-consistent reaction field method) are systematically studied using density functional theory. Spontaneous formation of certain multinuclear Fe(III) oxyhydroxide clusters with clear structural signatures of ferrihydrite highlights their potential as prenucleation clusters in the course of mineralization.
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页码:652 / 661
页数:10
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