Earth-abundant transition
metal phosphides are promising materials
for energy-related applications. Specifically, copper(I) phosphide
is such a material and shows excellent photocatalytic activity. Currently,
there are substantial research efforts to synthesize well-defined
metal–semiconductor nanoparticle heterostructures to enhance
the photocatalytic performance by an efficient separation of charge
carriers. The involved crystal facets and heterointerfaces have a
major impact on the efficiency of a heterostructured photocatalyst,
which points out the importance of synthesizing potential photocatalysts
in a controlled manner and characterizing their structural and morphological
properties in detail. In this study, we investigated the interface
dynamics occurring around the synthesis of Ag–Cu3P nanoparticle heterostructures by a chemical reaction between Ag–Cu
nanoparticle heterostructures and phosphine in an environmental transmission
electron microscope. The major product of the Cu–Cu3P phase transformation using Ag–Cu nanoparticle heterostructures
with a defined interface as a template preserved the initially present
Ag{111} facet of the heterointerface. After the complete transformation,
corner truncation of the faceted Cu3P phase led to a physical
transformation of the nanoparticle heterostructure. In some cases,
the structural rearrangement toward an energetically more favorable
heterointerface has been observed and analyzed in detail at the atomic
level. The herein-reported results will help better understand dynamic
processes in Ag–Cu3P nanoparticle heterostructures
and enable facet-engineered surface and heterointerface design to
tailor their physical properties.