<p>This
work shows that ZnTe/CdSe core/shell quantum dots synthesized by standard
literature procedures in actuality have an alloyed Cd<sup></sup><sub>x</sub>Zn<sub>1-x</sub>Te
core. We employ X-ray absorption spectroscopy (XAS) at all four <i>K</i>-shell
ionization edges (Zn, Te, Cd, Se) and perform a global fitting analysis in
order to extract the first-shell bond distances. We combine our XAS results
with transmission electron microscopy (TEM) sizing and elemental analyses,
which allows us to propose models of the internal particle structure. Our
multimodal characterization approach confirms <b>(1) </b>the presence of Cd-Te bonds, <b>(2) </b>cation<b> </b>alloying in the particle core (and the
absence of anion alloying), and <b>(3) </b>a
patchy pure-phase CdSe shell. We synthesize particles of different shell
thicknesses and performed synthetic control studies that allowed us to discard a
ZnTe/CdTe/CdSe core/shell/shell structure and confirm the alloyed core/shell
structure. Our structural analysis is
extended with electronic band structure calculations and UV/vis absorption spectroscopy,
demonstrating that the alloyed Cd<sup></sup><sub>x</sub>Zn<sub>1-x</sub>Te/CdSe
core/shell quantum dots exhibit a direct band gap, different from the predicted
type-II band alignment of the intended ZnTe/CdSe core/shell quantum dots. This study highlights the challenges with
synthesizing II-VI quantum dot heterostructures and the power of XAS for
understanding the internal structure of heterogenous nanoparticles.</p>