Electrochemical
surface science of oxides is an emerging field
with expected high impact in developing, for instance, rationally
designed catalysts. The aim in such catalysts is to replace noble
metals by earth-abundant elements, yet without sacrificing activity.
Gaining an atomic-level understanding of such systems hinges on the
use of experimental surface characterization techniques such as scanning
tunneling microscopy (STM), in which tungsten tips have been the most
widely used probes, both in vacuum and under electrochemical conditions.
Here, we present an in situ STM study with atomic
resolution that shows how tungsten(VI) oxide, spontaneously generated
at a W STM tip, forms 1D adsorbates on oxide substrates. By comparing
the behavior of rutile TiO2(110) and magnetite Fe3O4(001) in aqueous solution, we hypothesize that, below
the point of zero charge of the oxide substrate, electrostatics causes
water-soluble WO3 to efficiently adsorb and form linear
chains in a self-limiting manner up to submonolayer coverage. The
1D oligomers can be manipulated and nanopatterned in situ with a scanning probe tip. As WO3 spontaneously forms
under all conditions of potential and pH at the tungsten–aqueous
solution interface, this phenomenon also identifies an important caveat
regarding the usability of tungsten tips in electrochemical surface
science of oxides and other highly adsorptive materials.