Transition
metal dichalcogenides (TMDs) are attractive materials
for a variety of applications in solar energy conversion and electrocatalysis,
due to their favorable optical and electrical properties and their
unique two-dimensional structures which facilitate the fabrication
of wide-area, ultrathin layers. Unfortunately, the basal planes which
make up the majority of these materials are relatively inert, and
thus a great deal of effort has been directed to engineering favorable,
catalytically active defects into these materials. Here, we demonstrate
how probe-based electrochemical techniques can be employed as multifunctional
tools for locally modifying TMD materials and probing the electrochemical
behavior of the resulting defects. Scanning Electrochemical Cell Microscopy
(SECCM) was employed to locally anodize exfoliated p-type WSe2 nanosheets, creating hole-like defects within individual
basal planes in a highly controllable fashion. Photoelectrochemical
SECCM imaging was then employed to characterize the chemical behavior
of these engineered defects, revealing significantly enhanced activity
toward the Hydrogen Evolution Reaction (HER). Atomic force microscopy
studies are presented which suggest these enhancements result from
an increased density of monolayer-high step features within the anodized
defects. Analysis of the SECCM data in the context of finite element
simulations revealed that these enhancements increased with increasing
anodization time, with local kinetic rates over 2 orders of magnitude
higher than unaltered basal planes.