High-resolution structural study of zinc ion incorporation at the calcite cleavage surface

被引:45
作者
Cheng, L
Sturchio, NC [1 ]
Woicik, JC
Kemner, KM
Lyman, PF
Bedzyk, MJ
机构
[1] Argonne Natl Lab, Div Environm Res, Argonne, IL 60439 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Mat Res Ctr, Evanston, IL 60208 USA
[4] Natl Inst Stand & Technol, Gaithersburg, MD 20899 USA
[5] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
adsorption; calcite; surface extended x-ray absorption fine structure (SEXAFS); surface structure; X-ray standing waves (XSW); zinc;
D O I
10.1016/S0039-6028(98)00545-7
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
The atomic-scale structure of Zn2+ incorporated at the CaCO3 (10 (1) over bar 4) surface by adsorption from solution was determined by X-ray standing wave triangulation and surface extended X-ray absorption fine structure spectroscopy. At low coverage (approximately 0.1 ML), Zn2+ substitutes for Ca2+ in the surface layer. Structural relaxation of the adjacent in-plane CO32- ions in the host surface is shown by the reduced nearest-neighbor distance of Zn-O relative to Ca-O. Relaxation of the Zn2+ ion in the out-of-plane direction is shown by the displacement of its lattice position from the ideal Ca2+ position. These relaxations, resulting in a local lattice buckling feature at the Zn2+ adsorption site, can be fully explained as the combined effect of the electrostatic relaxation of the nearest-neighbor anions in response to the smaller size of Zn2+, and the bonding asymmetry due to surface truncation. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:L976 / L982
页数:7
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