Muscovite mica is an important mineral that has become a standard substrate, due to its easy cleavage along the {001} planes, revealing a very flat surface that is compatible with many biological materials. Here we study mica surfaces by dynamic atomic force microscopy (AFM) operated in the non-contact mode (NC-AFM) under ultra-high vacuum (UHV) conditions. Surfaces produced by cleaving in UHV cannot be imaged with NC-AFM due to large surface charges; however, cleavage in air yields much less surface charge and allows for NC-AFM imaging. We present highly resolved NC-AFM images of air-cleaved mica surfaces revealing a rough morphology originating from a high density of nanometre-sized particles. Among these particles, we find regularly shaped structures indicating the growth of crystallites on the surface. The contamination layer cannot be removed by degassing in UHV; even prolonged heating at a temperature of 560 K under UHV conditions does not yield an atomically flat surface.

The stabilization of polar oxide surfaces is of fundamental interest for understanding many processes in surface chemistry. We study the zinc-terminated Zn-ZnO(0001), a surface important in heterogeneous catalysis, by highest resolution scanning force microscopy (SFM) operated in the noncontact mode (NC-AFM). While most of the surface morphology is dominated by a phase consisting of triangular shaped nanostructures, we observe a coexisting (1 × 3) reconstructed phase where the reconstruction is ascribed to the formation of missing Zn-rows. Our findings provide evidence that the electrostatic instability of the polar Zn-ZnO(0001) surface can be canceled by a reduction of the surface charge by 1/3 which is considerably larger than the value of 1/4 derived from a simple ionic model for polar stabilization. Within the presented model for the (1 × 3) reconstruction, the role of point defects tentatively ascribed to hydrogen adsorbed on top of double Zn-rows forming zinc-hydride is discussed.

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Non-contact atomic force microscopy is used to study C(60) molecules deposited on the rutile TiO(2)(110) surface in situ at room temperature. At submonolayer coverages, molecules adsorb preferentially at substrate step edges. Upon increasing coverage, ordered islands grow from the decorated step edges onto the lower terraces. Simultaneous imaging of bridging oxygen rows of the substrate and the C(60) island structure reveals that the C(60) molecules arrange themselves in a centered rectangular superstructure, with the molecules lying centered in the troughs formed by the bridging oxygen rows. Although the TiO(2)(110) surface exhibits a high density of surface defects, the observed C(60) islands are of high order. This indicates that the C(60) intermolecular interaction dominates over the molecule-substrate interactions that may cause structural perturbations on a defective surface. Slightly protruding C(60) strands on the islands are attributed to anti-phase boundaries due to stacking faults resulting from two islands growing together.

Atomic scale manipulation on insulating surfaces is one of the great challenges of non-contact atomic force microscopy. Here we demonstrate lateral manipulation of defects occupying single ionic sites on a calcium fluoride (111)-surface. Defects stem from the interaction of the residual gas with the surface. The process of surface degradation is briefly discussed. Manipulation is performed over a wide range of path lengths ranging from tens of nanometres down to a few lattice constants. We introduce a simple manipulation protocol based on line-by-line scanning of a surface region containing defects to be manipulated, and record tip-surface distance and cantilever resonance frequency detuning as a function of the manipulation pathway in real time. We suggest a hopping model to describe manipulation where the tip-defect interaction is governed by repulsive forces.