首页> 外文期刊>Chemphyschem: A European journal of chemical physics and physical chemistry >In Situ Observation of the Surface Processes Involved in Dissolution from the Cleavage Surface of Calcite in Aqueous Solution Using Combined Scanning Electrochemical-Atomic Force Microscopy (SECM-AFM)
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In Situ Observation of the Surface Processes Involved in Dissolution from the Cleavage Surface of Calcite in Aqueous Solution Using Combined Scanning Electrochemical-Atomic Force Microscopy (SECM-AFM)

机译:使用组合扫描电化学原子力显微镜(SECM-AFM)现场观察方解石从水溶液的裂解表面溶解所涉及的表面过程

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The surface processes involved in the initial stages of the proton-assisted dissolution of the calcite single crystal cleavage plane (101-bar4) have been identified using a combined scanning electrochemical-atomic force microscope (SECM-AFM). This instrument employs a platinum-coated AFM probe, which functions as an electrode as well as a high-resolution topographical sensor. Dissolution in this arrangement is effected by the local electro-generation of protons, produced by oxidation of water at the probe electrode. By careful control of the applied potential, it is possible to vary the magnitude of the electrogenerated flux of protons from the probe towards the calcite surface. Crucially, by generating a small proton flux for short time periods (0.5 s) it is possible to observe and monitor the initial sites in the dissolution process. Topographical images were recorded in the same area of the surface both prior to and after inducing dissolution, as a function of the proton flux. At low proton fluxes, of the order of 1 nmol cm~(-2)s~(-1) or less, the surface was observed to dissolve by the nucleation of monolayer deep pits, with densities of about 10~8 cm~(-2). These pits are likely to be formed at point vacancies or atomic (impurity, for example) defects in the crystal lattice. As the proton flux was increased (over two orders of magnitude), these same etch pits were found to open into wider macro-pits, with an outline morphology that reflected the crystallographic orientation of the surface. At the highest proton fluxes, dissolution from macroscopic step edges became significant.
机译:使用组合扫描电化学原子力显微镜(SECM-AFM)已确定了方解石单晶劈裂面(101-bar4)的质子辅助溶解初始阶段涉及的表面过程。该仪器采用镀铂的AFM探针,该探针既可以用作电极,又可以用作高分辨率的地形传感器。在这种布置中的溶解受质子的局部发电的影响,质子的产生是由探针电极上水的氧化产生的。通过仔细控制所施加的电势,可以改变从探针到方解石表面的质子的电生通量的大小。至关重要的是,通过在短时间内(0.5 s)产生小的质子通量,可以观察和监测溶解过程中的初始位置。根据质子通量,在诱导溶解之前和之后在表面的相同区域中记录地形图。在低质子通量(约1 nmol cm〜(-2)s〜(-1)或更低)下,观察到表面通过单层深凹核的溶解而溶解,密度约为10〜8 cm〜( -2)。这些凹坑很可能在晶格中的点空位或原子(例如杂质)缺陷处形成。随着质子通量的增加(超过两个数量级),发现这些相同的蚀刻凹坑通向更宽的宏观凹坑,其轮廓形态反映了表面的晶体学取向。在最高的质子通量下,宏观台阶边缘的溶解变得明显。

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