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部分催化球形胶体的扩散泳自推进

Diffusiophoretic self-propulsion for partially catalytic spherical colloids.

作者信息

de Graaf Joost, Rempfer Georg, Holm Christian

出版信息

IEEE Trans Nanobioscience. 2015 Apr;14(3):272-88. doi: 10.1109/TNB.2015.2403255. Epub 2015 Mar 2.

Abstract

Colloidal spheres with a partial platinum surface coating perform autophoretic motion when suspended in hydrogen peroxide solution. We present a theoretical analysis of the self-propulsion velocity of these particles using a continuum multi-component, self-diffusiophoretic model. With this model as a basis, we show how the slip-layer approximation can be derived and in which limits it holds. First, we consider the differences between the full multi-component model and the slip-layer approximation. Then the slip model is used to demonstrate and explore the sensitive nature of the particle's velocity on the details of the molecule-surface interaction. We find a strong asymmetry in the dependence of the colloid's velocity as a function of the level of catalytic coating, when there is a different interaction between the solute and solvent molecules and the inert and catalytic part of the colloid, respectively. The direction of motion can even be reversed by varying the level of the catalytic coating. Finally, we investigate the robustness of these results with respect to variations in the reaction rate near the edge between the catalytic and inert parts of the particle. Our results are of significant interest to the interpretation of experimental results on the motion of self-propelled particles.

摘要

部分表面涂有铂的胶体球悬浮在过氧化氢溶液中时会进行自泳运动。我们使用连续多组分自扩散电泳模型对这些粒子的自推进速度进行了理论分析。基于该模型,我们展示了如何推导滑移层近似以及它在哪些极限情况下成立。首先,我们考虑完整多组分模型与滑移层近似之间的差异。然后,使用滑移模型来证明和探索粒子速度对分子 - 表面相互作用细节的敏感性。当溶质与溶剂分子以及胶体的惰性部分和催化部分之间存在不同相互作用时,我们发现胶体速度随催化涂层水平的变化存在强烈的不对称性。甚至可以通过改变催化涂层的水平来反转运动方向。最后,我们研究了这些结果对于粒子催化部分和惰性部分之间边缘附近反应速率变化的稳健性。我们的结果对于解释自推进粒子运动的实验结果具有重要意义。

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