Syntheses of transition-metal dichalcogenides
(TMDs) using colloidal-chemistry approaches are gaining signifi cant interest in recent years, as these methods enable the
morphology and properties of the nanocrystals to be tuned for
targeted applications. In this work, by only varying the ligand used
during synthesis, we synthesized nanoflowers with oleic acid (OA)
and 1T′ phase dominated WSe2 nanosheets with oleylamine (OLA).
WSe2 nanocrystals show slower rate of formation for the metastable
1T′ phase. Surface chemistry analyses of the synthesized nanocryst als by solution NMR establish that neither of the ligands bind
strongly to the surface of nanocrystals but are in a dynamic
coordination with the WSe2 surface. A further examination of the
coordination of tungsten hexacarbonyl (W(CO)6) with the
respective ligands confirms that W(CO)6 decomposes in OA, losing its octahedral symmetry, which leads to fast reactivity in the
flask. In contrast to this, W(CO)6 reacts with OLA to form a new complex, which leads to slower reactivity and crystallization of the
synthesized nanocrystals in the octahedral 1T′ phase. These insights into the influence of precursor-ligand chemistry on reaction
outcome and the peculiar surface chemistry of colloidal TMD nanocrystals will be instrumental in developing future colloidal TMD
nanocrystals.