Near molecular-scale growth of natural minerals: Experimental methods and errors in length-dependent step speeds with scanning probe microscopy |
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Authors: | Steven R Higgins Xiaoming Hu |
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Institution: | Chemistry Department, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH 45435, USA |
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Abstract: | Experimental observation of step (i.e., a linear discontinuity in a surface) growth on calcium carbonate and barium sulfate surfaces was performed using in situ scanning probe microscopy (SPM) in aqueous solutions. Step speeds at very short step lengths (<300 nm) were found to increase with step length, but scatter in the data precluded comparison of different theoretical models with regard to the experimental data. Analysis of experimental errors revealed that the data scatter was not unusual and further suggested that significant experimental bias in the determination of step properties such as the step free energy and kinetics of kink propagation and nucleation are introduced if the instrument bandwidth is not appropriate for the specific dynamics of the step. In light of step growth models based on either equilibrium assumptions or non-equilibrium assumptions, these biases tend to favor one model over the other. |
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Keywords: | Scanning probe microscopy Surface chemistry Heterogeneous kinetics Crystal growth Step dynamics Calcium carbonate Barium sulfate |
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