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The scanning tunnelling microscope (STM) has been a valuable tool in surface science for the study of structures and electronic states of metal surfaces. The recent advance of STM as a state-of-the-art technique to probe and manipulate individual molecules has made it possible to investigate molecular dynamics and chemical reactions at the surface in a single-molecule limit. In this review paper, we present an overview of our recent work of H-bond imaging, manipulating and engineering at a metal surface. From individual water molecules, a variety of H-bonded structures including water clusters, hydroxyl clusters and water–hydroxyl complexes are assembled on Cu(1 1 0), whose properties and dynamics are studied in real space in collaboration with density-functional-theory calculations.
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Okuyama et al. (2011) studied this question.
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