Physics of Complex Fluids Group and MESA+ Institute, Faculty of Science and Technology, University of Twente, PO Box 217, 7500 AE Enschede, The Netherlands.
Nanoscale. 2017 Apr 6;9(14):4721-4729. doi: 10.1039/c6nr09491k.
We use high resolution Atomic Force Microscopy to study the surface charge of the basal plane of gibbsite nanoparticles, with a lateral resolution of approximately 5 nm, in ambient electrolyte of variable pH and salt content. Our measurements reveal surface charge variations on the basal planes that correlate with the presence of topographic defects such as atomic steps. This surface charge heterogeneity, which increases with increasing pH, suggests that for a pH between 6 and 9 the defect sites display a stronger chemical activity than adjacent, apparently atomically smooth regions of the basal plane. Smooth regions display a slight positive surface charge of ≈0.05e per nm that hardly varies within this pH range. In contrast, near the topographic defects we observe a much lower charge. Considering the size of the interaction area under the probing tip, this implies that at the defect sites the charge density must be negative, ≈-0.1e per nm. These measurements demonstrate that surface defects have a large influence on the average surface charge of the gibbsite basal plane. These findings will contribute to understand why surface defects play an important role in various applications, such as fuel cells, chemical synthesis, self-assembly, catalysis and surface treatments.
我们使用高分辨率原子力显微镜研究了水铝石纳米粒子基面的表面电荷,其横向分辨率约为 5nm,在可变 pH 值和盐含量的环境电解质中进行测量。我们的测量结果揭示了与地形缺陷(如原子台阶)相关的基面表面电荷变化。这种表面电荷异质性随着 pH 值的增加而增加,这表明在 pH 值为 6 至 9 之间,缺陷部位显示出比相邻的、明显原子平滑的基面区域更强的化学活性。平滑区域显示出约 0.05e/每 nm 的轻微正表面电荷,在该 pH 范围内几乎没有变化。相比之下,在地形缺陷附近,我们观察到的电荷要低得多。考虑到探测尖端下的相互作用面积大小,这意味着在缺陷部位,电荷密度必须为负,约为-0.1e/每 nm。这些测量结果表明,表面缺陷对水铝石基面的平均表面电荷有很大影响。这些发现将有助于理解为什么表面缺陷在各种应用中(如燃料电池、化学合成、自组装、催化和表面处理)起着重要作用。